Clinical trials

26

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Condition / disease
Location
Status: Recruiting

The Effect of Peloidotherapy in Young Adults Undergoing Physical Therapy Scoliosis Specific Exercises (PSSE)

Scoliosis is a musculoskeletal disorder defined by a three-dimensional spinal deformity that can result in substantial clinical and functional limitations, particularly during adolescence and young adulthood. Affected individuals commonly experience postural asymmetry, muscular imbalance, pain, and diminished quality of life. In conservative management, Physiotherapeutic Scoliosis-Specific Exercises (PSSE) have gained recognition as a fundamental intervention. The primary objectives of PSSE include optimizing spinal alignment, facilitating rotational breathing, and restoring muscular symmetry to improve functional capacity. Evidence from systematic reviews suggests that PSSE, especially the Schroth method, are superior to general exercise programs in improving both radiographic parameters and health-related quality of life.Meta-analytic findings further support the effectiveness of PSSE in reducing curve magnitude and enhancing quality of life outcomes. Among the various PSSE approaches, the Schroth method is one of the most extensively investigated and widely applied in clinical settings. This method incorporates three-dimensional postural correction, targeted breathing techniques, and the development of postural awareness. Randomized controlled trials have demonstrated that Schroth exercises significantly improve SRS-22 quality of life scores and positively influence pain, body image, and overall well-being.Despite these established benefits, pain and muscle tension occurring during exercise sessions may negatively influence adherence to rehabilitation programs. In young adults, pain is a critical factor limiting treatment compliance and restricting engagement in daily activities. Accordingly, adjunctive interventions implemented prior to exercise may enhance exercise tolerance and optimize therapeutic outcomes.Peloidotherapy, which involves the therapeutic application of natural medicinal mud, is commonly used in musculoskeletal rehabilitation due to its analgesic, muscle-relaxant, and circulation-enhancing effects. By alleviating pain and reducing muscular tension, peloidotherapy may facilitate greater participation in exercise programs and support improved clinical outcomes.This study aims to investigate the effects of adjunctive peloidotherapy administered before Schroth-based PSSE in young adults with scoliosis, focusing on pain, exercise adherence, and quality of life, with particular emphasis on SRS-22 measures..

Participants needed: 54
Trial details
Age: 20-40Biological sex: AllType: ObservationalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Jun 10, 2026Locations: 1Duration: 4 Months
Eligibility criteria

Aged 20-40 years [+6]

Individuals who have undergone scoliosis surgery [+6]

Status: Recruiting

Effects of Aquatic Exercise in Older Adults With Sarcopenia:A Randomized Trial

Sarcopenia is a geriatric syndrome characterized by age-related loss of skeletal muscle mass, strength, and physical performance, leading to increased risk of falls, functional decline, and reduced quality of life. Exercise interventions, particularly resistance training, are effective in managing sarcopenia; however, land-based exercises may be challenging for older adults due to balance impairments, joint problems, and fear of falling. Pool-based exercise programs may offer a safe and feasible alternative, as water buoyancy reduces joint loading while providing resistance to support muscle strengthening. Despite these potential benefits, evidence regarding the effects of aquatic exercise in individuals with sarcopenia remains limited, especially in Türkiye. This study aims to evaluate the effects of a 6-week supervised pool-based exercise program on muscle strength, muscle morphology, physical performance, mood, and quality of life in individuals aged 65 years and older with sarcopenia. Sarcopenia will be identified using the Sonographic Thigh Adjustment Ratio (STAR), based on ultrasound measurements of anterior thigh muscle thickness. In addition, appendicular skeletal muscle mass will be assessed using bioelectrical impedance analysis (ASM/height²). Outcome measures will include ultrasound-based muscle thickness, STAR, muscle strength, functional performance tests, depressive symptoms, and health-related quality of life. Assessments will be performed at baseline, immediately after the intervention, and at 1-month follow-up.

Participants needed: 44
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: May 12, 2026Locations: 2
Eligibility criteria

Age ≥65 years [+5]

Inability to complete assessment tests and questionnaires [+9]

Status: Not yet recruiting

Ai Chi-Based Rehabilitation for Peripheral Unilateral Vestibular Dysfunction

This study aims to evaluate the effects of an Ai Chi-based rehabilitation program on balance, dizziness severity, and quality of life in patients with unilateral peripheral vestibular hypofunction. Participants will be randomly assigned to either a control group receiving standard home-based vestibular rehabilitation exercises or an intervention group receiving additional Ai Chi sessions. The intervention will be conducted over a 4-week period with a total of 10 sessions under the supervision of a certified therapist.

Participants needed: 38
Trial details
Age: 18-70Biological sex: FemaleType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: May 7, 2026
Eligibility criteria

Age between 18 and 70 years [+5]

Inability to complete assessment tests and questionnaires [+7]

Status: Recruiting

Ultrasound-Guided Dextrose Prolotherapy for Coccydynia: A Prospective Study

Coccydynia is a musculoskeletal condition characterized by pain in the coccygeal region, particularly exacerbated by sitting, and is associated with impaired quality of life and functional limitation. Although various conservative and interventional treatment options are available, there remains a need for effective and safe alternative therapies, especially in treatment-resistant cases. Prolotherapy is a regenerative treatment modality that aims to reduce pain and improve function by stimulating tissue repair, particularly in ligamentous structures. While there is increasing evidence supporting its effectiveness in mechanical musculoskeletal pain conditions, the literature regarding its use in coccydynia is limited. The aim of this study is to evaluate the effect of dextrose prolotherapy on pain severity and functional status in patients diagnosed with coccydynia. This study is designed as a prospective, single-arm, open-label interventional study. Patients will receive 15% dextrose prolotherapy according to a standardized protocol. Pain severity will be assessed using the Visual Analog Scale (VAS), and functional status will be evaluated using the Dallas Pain Questionnaire before treatment and at 1 month after completion of the treatment. This study aims to provide more comprehensive data on the effectiveness and safety of prolotherapy in coccydynia and to contribute to the currently limited evidence in the literature.

Participants needed: 30
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: May 4, 2026Locations: 1
Eligibility criteria

Age between 18 and 75 years [+2]

Age <18 years or >75 years [+9]

Status: Recruiting

Oral vs. Intravenous Hydration to Prevent Contrast-Associated Acute Kidney Injury in the ED

This study is planned to be conducted by emergency physicians between November 7, 2025, and December 7, 2026. Inclusion and Exclusion Criteria The study will include adult patients aged 18 years and older who are considered at risk for Contrast-Associated Acute Kidney Injury (CA-AKI), with an estimated Glomerular Filtration Rate (eGFR) between 15-59 ml/min/1.73 m², a clinical indication for contrast-enhanced CT, and who have provided signed informed consent. Exclusion criteria are as follows: Pregnant women. Patients with a known contrast media allergy. Contrast media exposure within the last 72 hours. End-stage renal disease (ESRD) with eGFR \<15 ml/min/1.73 m² or those receiving dialysis. Patients with clinical decompensated heart failure. Patients for whom oral intake is contraindicated or not tolerated. Randomization and Interventions Prior to randomization, the oral intake capacity of eligible patients will be verified. Participants will be randomized into two groups-IV hydration and oral hydration-at a 1:1 ratio using stratified block randomization based on age and gender. IV Hydration Group: Isotonic 0.9% NaCl solution will be administered. The regimen consists of 3 ml/kg for 1 hour pre-procedure, followed by 2 ml/kg/hour for 4 hours post-procedure. Patients with an ejection fraction (EF) \<40% will receive half-doses (1.5 ml/kg pre-procedure; 1 ml/kg/hour for 4 hours post-procedure). Oral Hydration Group: Drinking water will be administered under nursing supervision. The regimen consists of 500 ml 1 hour pre-procedure and 125 ml/hour for 4 hours post-procedure. Patients with an EF \<40% will receive half-doses (250 ml pre-procedure; 62.5 ml/hour post-procedure). Follow-up and Outcome Measures Baseline renal function tests will be obtained from all patients prior to the protocol. Patients will be re-evaluated for CA-AKI via blood samples taken 48-72 hours after contrast administration. Furthermore, eGFR changes will be calculated using the Modification of Diet in Renal Disease (MDRD) formula. Mehran Risk Scores will also be determined for each patient. Long-term outcomes, including progression to ESRD (requirement for dialysis) and mortality within 1 month, as well as creatinine levels between days 30-45, will be assessed.

Participants needed: 198
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Mar 9, 2026Locations: 1
Eligibility criteria

Patients aged 18 years and older. [+3]

Pregnant women. [+5]

Status: Recruiting

The Effect of Three-Dimensional Exercises ( Schroth Method ) on Trunk Muscle Endurance, Sleep Quality, and Quality of Life in Adolescents With Hyperkyphosis

Adolescence is a critical period for spinal growth, and progression of thoracic hyperkyphosis may lead to pain, weak trunk muscles, sleep disturbances, and reduced quality of life. This study aims to investigate the effects of three-dimensional exercise program based on the Schroth Method on trunk muscle endurance, thoracic kyphosis angle, pain, sleep quality and quality of life in adolescents aged 12-18 years with hyperkyphosis.

Participants needed: 60
Trial details
Age: 12-18Biological sex: AllType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Feb 11, 2026Locations: 1
Eligibility criteria

Adolescents between 12 and 18 years of age [+4]

Scoliosis with a Cobb angle >10° in the coronal plane [+8]

Status: Not yet recruiting

Evaluation of the Effects of Adenoidectomy and Adenotonsillectomy on Voice in Children

This prospective study aims to evaluate the effects of adenoidectomy and adenotonsillectomy on voice and speech functions in children. Changes in voice quality and resonance may occur after the removal of adenoid and tonsillar tissues, particularly in pediatric patients with enlarged adenoids or tonsils. Objective voice assessments, including acoustic, aerodynamic, and nasalance measurements, as well as subjective voice-related quality of life questionnaires, will be performed before surgery and at the first and third months after surgery. The results of this study are expected to help clinicians better inform families about possible voice changes following adenoidectomy and adenotonsillectomy procedures.

Participants needed: 36
Trial details
Age: 4-13Biological sex: AllType: ObservationalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Feb 10, 2026Locations: 1
Eligibility criteria

Aged 4-13 years [+1]

Does not meet inclusion criteria [+10]

Status: Recruiting

Ultrasonographic Evaluation of Talar Cartilage Thickness in Patients With Spinal Cord Injury

Spinal cord injury patients often present with musculoskeletal comorbidities, including osteoarthritis. Early detection of cartilage damage is important for preventing osteoarthritis progression. This study aims to compare the talar cartilage thicknesses of spinal cord injury patients with healthy subjects. The secondary aim is to investigate a correlation between the talar cartilage thickness and disease-related parameters. The patient group is to be assessed for talar cartilage thickness (via ultrasound), functional status, spasticity, and ambulation levels.

Participants needed: 76
Trial details
Age: 18-60Biological sex: AllType: ObservationalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Feb 2, 2026Locations: 1
Eligibility criteria

Aged between 18 to 60 years, [+5]

Patients with sacral level injury [+6]

Status: Recruiting

Proximal Versus Distal Superior Cluneal Nerve Block in Entrapment Neuropathy

Superior cluneal nerve (SCN) entrapment is an underdiagnosed cause of chronic low back and gluteal pain. Although diagnostic nerve block is considered the gold standard for confirming SCN entrapment, there is no consensus regarding the optimal injection approach. This prospective observational study aims to compare the clinical effectiveness of proximal and distal ultrasound-guided SCN block techniques in patients diagnosed with SCN entrapment. Pain intensity and functional outcomes will be evaluated over the follow-up period to assess differences between the two approaches.

Participants needed: 54
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Jan 28, 2026Locations: 1Duration: 3 Months
Eligibility criteria

Age between 18 and 75 years [+5]

Active local or systemic infection [+11]

Status: Recruiting

Thyroid-Stimulating Hormone Levels in Pregnancy and Their Association With Depression, Anxiety, and Sexual Function

This prospective, single-center, observational cross-sectional study aims to evaluate the relationship between thyroid-stimulating hormone (TSH) levels and psychological as well as sexual health outcomes during pregnancy. Pregnant individuals will undergo psychometric assessment using the Beck Depression Inventory (BDI), Beck Anxiety Inventory (BAI), the Arizona Sexual Experience Scale (ASEX), and the YKK-13 Quality of Life Scale. The study will investigate whether maternal TSH levels are associated with depression, anxiety, sexual function, and overall quality of life scores. Eligible participants will be pregnant women aged 18-45 years with a singleton pregnancy of at least 6 weeks, who are literate and have provided informed consent. Individuals with a prior psychiatric history, multiple gestation, or existing systemic or endocrine diseases will be excluded. The primary endpoint of the study is to determine the association between TSH levels and psychometric scale scores during pregnancy.

Participants needed: 180
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Dec 9, 2025Locations: 1Duration: 1 Month
Eligibility criteria

Not listed

Status: Recruiting

Analgesic Efficacy of Quadratus Lumborum vs. Transversalis Fascia Block in Inguinal Hernia Surgery

It is planned to compare the postoperative analgesic efficacy of the Transversalis Fascia Plane Block and the anterior Quadratus Lumborum Block in elective inguinal hernia surgeries.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Dec 1, 2025Locations: 1
Eligibility criteria

Ages 18-65 [+1]

Allergy to local anesthetics [+6]

Status: Recruiting

Timing of LNG-IUD Insertion and Ovarian Cyst Formation

In this prospective observational study, the effect of timing of insertion (early/late follicular; early/late luteal) on ovarian cyst development in women receiving an LNG-IUD will be assessed ultrasonographically at months 0, 3, 6, and 12. Secondary outcomes include cyst size/structure, bleeding pattern, pain, and other adverse events.

Participants needed: 60
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Nov 25, 2025Locations: 1Duration: 1 Year
Eligibility criteria

Reproductive age: 18-45 years [+6]

Pregnancy history or current pregnancy [+7]

Status: Recruiting

Hemodynamic Effects of Surgical Position in Prone vs. Supine Percutaneous Nephrolithotomy

This prospective, randomized controlled study evaluates the hemodynamic effects of prone and supine positions during percutaneous nephrolithotomy (PNL) for large kidney stones. Surgical position may influence intraoperative and postoperative hemodynamic stability. Prone positioning can increase intrathoracic pressure and reduce venous return, whereas supine positioning may provide greater hemodynamic stability. A total of 84 patients will be randomized to undergo PNL in prone or supine positions. Primary outcomes include changes in hemodynamic parameters during surgery. Results may guide surgical position selection, especially in patients with potential hemodynamic risk.

Participants needed: 84
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Aug 24, 2025Locations: 1
Eligibility criteria

ASA physical status I-III [+1]

Pregnancy [+7]

Status: Recruiting

PPI in Weaning Prediction

The aim of this study is to evaluate the predictive role of the Peripheral Perfusion Index (PPI) in forecasting extubation success during the weaning process in intensive care unit (ICU) patients. The study will investigate the ability of PPI to predict extubation failure by comparing it with traditional weaning criteria, including the Rapid Shallow Breathing Index (RSBI), PaO₂/FiO₂ ratio, and respiratory rate.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Aug 13, 2025Locations: 1
Eligibility criteria

Patients who have been on mechanical ventilation for at least 48 hours [+2]

Patients for whom extubation is not planned due to hemodynamic instability [+2]

Status: Recruiting

VNOTES Approach in Mesh Free Sacrocolpopexy: A Functional and Anatomic Evaluation

This study aims to evaluate the effectiveness of mesh-free sacrocolpopexy performed using the VNOTES (Vaginal Natural Orifice Transluminal Endoscopic Surgery) technique in the surgical treatment of pelvic organ prolapse. Anatomical and functional outcomes will be assessed over a 6-month period before and after the operation. Evaluation tools will include the Pelvic Floor Distress Inventory-20 (PFDI-20), Pelvic Organ Prolapse Quantification (POP-Q) system, and the Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire (PISQ-12). The findings of this study are expected to provide important data on the anatomical improvement, functional outcomes, and impact on sexual function of mesh-free sacrocolpopexy performed via the VNOTES approach.

Participants needed: 26
Trial details
Age: 18-75Biological sex: FemaleType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Aug 11, 2025Locations: 2
Eligibility criteria

Not listed

Status: Recruiting

Comparison of vNOTES and Laparoscopic Salpingectomy in the Surgical Treatment of Ectopic Pregnancy

This study compares vNOTES salpingectomy and laparoscopic salpingectomy in the treatment of ectopic pregnancy, focusing on outcomes such as operative time, postoperative pain, and recovery.

Participants needed: 56
Trial details
Age: 18-55Biological sex: FemaleType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Aug 5, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Transperineal Ultrasound Evaluation of Vesicourethral Angle and de Novo SUI After Colpocleisis Surgery

This prospective observational study aims to evaluate changes in the vesicourethral angle using transperineal ultrasound before and after colpocleisis surgery, and to assess the relationship of these changes with the development of de novo stress urinary incontinence.

Participants needed: 31
Trial details
Age: 60-75Biological sex: FemaleType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Jul 17, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Post-Hysterectomy Vaginal Length: Horizontal vs. Vertical Closure

This prospective clinical study aims to evaluate the impact of vaginal cuff closure orientation-horizontal versus vertical-on postoperative total vaginal length in patients undergoing vaginal hysterectomy combined with lateral suspension. By comparing anatomical outcomes between the two closure techniques, the study seeks to determine which method better preserves vaginal length, potentially influencing surgical preferences and postoperative quality of life.

Participants needed: 62
Trial details
Age: 35-65Biological sex: FemaleType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Jul 16, 2025Locations: 1
Eligibility criteria

Cases with vaginal hysterectomy and lateral suspension surgery due to stage 3-4...

Cases that have previously undergone a different suspension surgery due to desce...

Status: Not yet recruiting

Low- vs. Normal-Flow Anesthesia and Delirium After Hip Fracture in the Elderly

The aim of this study is to investigate the relationship between low-flow and normal-flow anesthesia techniques and the development of postoperative delirium in elderly patients undergoing surgery for hip fracture.

Participants needed: 128
Trial details
Age: 65+Biological sex: AllType: ObservationalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: May 15, 2025
Eligibility criteria

Not listed

Status: Recruiting

Effects of Hydrotherapy in Children With Cerebral Palsy

The goal of this observational study is to learn the effects of hydrotherapy in children with cerebral palsy. It aims to answer if hydrotherapy is affective on balance and selective motor control of the children with cerebral palsy.

Participants needed: 36
Trial details
Age: 4-18Biological sex: AllType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Mar 27, 2025Locations: 1
Eligibility criteria

Diagnosed with Cerebral Palsy by a specialist physician [+4]

Mental retardation or insufficient cognitive function to comply with study asses... [+9]

Status: Recruiting

Efficacy of Variable Volume Truncal Blocks in Upper Limb Orthopedic Surgery

aim of this study is to compare the effect of selective truncal blocks, performed at different doses and volumes, on the onset times of motor and sensory blocks required for anesthesia in patients scheduled for hand, wrist, forearm, and elbow surgeries. Completing the operation under regional anesthesia will be considered a successful block.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Mar 5, 2025Locations: 1
Eligibility criteria

ASA 1-2 [+2]

Patient refusal [+12]

Status: Recruiting

Effects of Hydrotherapy on Unilateral Lower Extremity Lymphedema

Lymphedema is a chronic condition that negatively affects patients' quality of life and lower extremity functions, causing swelling and a feeling of heaviness in the extremity, as well as posing an economic burden. The gold standard in lymphedema treatment is complex decongestive therapy.Manual lymphatic drainage, skin care, the use of compression garments, and home exercise programs play an important role. Exercise therapies lead to a reduction in volume and an improvement in functionality and quality of life in patients with lymphedema. However, studies on this subject have mostly focused on upper extremity lymphedema. This study aims to compare the effects of a home exercise program and hydrotherapy combined with a home exercise program on quality of life, lower extremity functionality, exercise capacity, and edema severity in patients with unilateral lower extremity lymphedema

Participants needed: 52
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Feb 21, 2025Locations: 1
Eligibility criteria

Patients with primary or secondary unilateral lower extremity lymphedema diagnos... [+4]

Patients who are unable to perform the evaluation parameters [+6]

Status: Recruiting

Evaluation of Perioperative Cystoscopy and Methylene Blue Test in Detecting Complications in TVT and TOT Procedures

Comparison of complications detected by perioperative cystoscopy combined with methylene blue test and postoperative cystoscopy in TVT and TOT operations.

Participants needed: 58
Trial details
Age: 18-85Biological sex: FemaleType: InterventionalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Feb 6, 2025Locations: 1
Eligibility criteria

Providing consent to participate in the study [+8]

Not providing consent to participate in the study [+8]

Status: Recruiting

Comparison of Postoperative Outcomes of Laparoscopic Lateral Suspension and V-NOTES Lateral Suspension With the Salman Ketenci Gencer Technique

Comparison of Early Postoperative Outcomes of Patients Undergoing Laparoscopic Lateral Suspension and V-NOTES Lateral Suspension with the Salman Ketenci Gencer Technique

Participants needed: 84
Trial details
Age: 18-75Biological sex: FemaleType: ObservationalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Jan 31, 2025Locations: 1
Eligibility criteria

Patients with stage 3 or 4 pelvic organ prolapse Sexually active patients

Cervical pathology History of loop electrosurgical excision procedure (LEEP) or...

Status: Recruiting

Comparison of Five-year Survival and Disease-free Survival in Patients Diagnosed With Endometrium Cancer Who Underwent Total Laparoscopic Hysterectomy With and Without Uterine Manipulator

Comparison of five-year survival and disease-free survival in patients diagnosed with endometrium cancer who underwent total laparoscopic hysterectomy with and without a uterine manipulator

Participants needed: 108
Trial details
Age: 18-75Biological sex: FemaleType: ObservationalSponsor: Gaziosmanpasa Research and Education HospitalUpdated: Jan 7, 2025Locations: 1
Eligibility criteria

patients suitable for laparoscopic surgery patients ages 18-75 patients diagnose...

patients not suitable for laparoscopic surgery patients diagnosed figo stage 3 a...