Clinical trials

7

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

HFNC for Postoperative Atelectasis After Laparoscopic Surgery

Pneumoperitoneum and Trendelenburg positioning during laparoscopic surgery promote atelectasis development, which has been reported in up to 90% of patients under general anesthesia and increases the risk of postoperative pulmonary complications. High-flow nasal cannula (HFNC) oxygen therapy may reduce post-extubation atelectasis through alveolar recruitment. This prospective observational cohort study aims to evaluate the role of HFNC in postoperative atelectasis monitored by lung ultrasonography (LUS) in patients undergoing elective laparoscopic surgery.

Participants needed: 90
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Bursa Yuksek Ihtisas Training and Research HospitalUpdated: Jun 30, 2026
Eligibility criteria

Adult patients aged 18 years and older [+4]

Severe or uncontrolled chronic obstructive pulmonary disease, asthma, or other c... [+6]

Status: Not yet recruiting

vNOTES vs Laparoscopy: Respiratory Mechanics and Hemodynamics

Pneumoperitoneum and Trendelenburg position are unavoidable in laparoscopic surgery and are known to have adverse effects on intraoperative respiratory mechanics and hemodynamics. These conditions increase the risk of ventilator-induced lung injury (VILI) and highlight the importance of lung-protective ventilation strategies. vNOTES (Vaginal Natural Orifice Transluminal Endoscopic Surgery) is a minimally invasive technique that requires less Trendelenburg tilt and lower insufflation pressures compared to conventional laparoscopic surgery, and may therefore offer a more favorable intraoperative profile. This prospective, observational, single-center, parallel-group cohort study aims to compare respiratory mechanics parameters (Ppeak, Pplateau, DP, MPtot, MPdyn, Crs) and hemodynamic parameters (MAP, HR, vasopressor requirement) between vNOTES (n=15) and laparoscopic gynecological surgery (n=15) groups at four intraoperative time points.

Participants needed: 30
Trial details
Age: 18-75Biological sex: FemaleType: ObservationalSponsor: Bursa Yuksek Ihtisas Training and Research HospitalUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Female patients aged 18 to 75 years [+4]

Severe or uncontrolled chronic obstructive pulmonary disease, asthma, or other c... [+6]

Status: Recruiting

Socio-Cultural Level, Health Literacy, and Parental CT Demand in Paediatric Minor Head Trauma

Minor head trauma is one of the most frequent reasons for paediatric emergency department visits worldwide. The PECARN (Paediatric Emergency Care Applied Research Network) clinical decision rule stratifies children with minor head trauma into low-, intermediate-, and high-risk categories for clinically important traumatic brain injury (ciTBI) and provides evidence-based guidance on computed tomography (CT) ordering. Despite its high diagnostic accuracy, real-world CT utilisation frequently diverges from PECARN recommendations. Non-clinical family-level factors - including socio-cultural characteristics and health literacy - may drive part of this divergence, particularly through their influence on whether families explicitly request CT imaging. This prospective observational cohort study will enrol 200 children with minor head trauma presenting to the emergency department of SBU Bursa Yuksek Ihtisas EAH, Bursa, Turkey. The primary aim is to determine whether family socio-cultural level (composite index incorporating education, occupation, income, and housing; scored 0-10) and health literacy (Newest Vital Sign-Turkish, NVS-TR) independently predict parental demand for CT imaging. Secondary aims include determining whether parental CT demand and family socio-cultural characteristics predict CT ordering by the treating physician, describing PECARN algorithm adherence patterns in this setting, and examining parental health-seeking behaviour at 7-day telephone follow-up.

Participants needed: 200
Trial details
Age: Up to 17Biological sex: AllType: ObservationalSponsor: Bursa Yuksek Ihtisas Training and Research HospitalUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Age less than 18 years at time of emergency department presentation [+3]

GCS score 13 or less at presentation (moderate or severe head injury) [+9]

Status: Not yet recruiting

Parasacral Ischial Plane Block in Lower Extremity Surgery

The parasacral ischial plane block is a novel fascial plane approach targeting the sacral plexus. This technique is technically less challenging and eliminates the requirement for direct visualization of the sacral plexus. The aim of this prospective observational study is to evaluate the efficacy of the conventional sacral plexus block versus the parasacral ischial plane block in patients undergoing lower extremity surgery.

Participants needed: 60
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Bursa Yuksek Ihtisas Training and Research HospitalUpdated: May 18, 2026Locations: 1
Eligibility criteria

Ages 18-80 [+4]

Patients with a history of allergy to local anesthetic drugs [+7]

Status: Recruiting

Optic Nerve Sheath Diameter and Cognitive Outcomes in Bentall Surgery

Bentall surgery is a major cardiac procedure involving replacement of the ascending aorta, aortic root, and aortic valve, typically requiring cardiopulmonary bypass (CPB) and sometimes deep hypothermic circulatory arrest (DHCA). Due to its complexity, it carries a significant risk of postoperative neurological complications including stroke and postoperative cognitive dysfunction (POCD). This prospective observational study aims to evaluate the relationship between perioperative bilateral optic nerve sheath diameter (ONSD) measurements obtained by ultrasound and postoperative cognitive functions in patients undergoing elective Bentall surgery. ONSD is a non-invasive surrogate marker of intracranial pressure that can be measured at the bedside using ultrasound. In addition to routine hemodynamic monitoring and cerebral oximetry (NIRS), bilateral ONSD will be measured at predefined intraoperative and postoperative time points. Cognitive function will be assessed using the Montreal Cognitive Assessment (MoCA) test preoperatively and postoperatively, and delirium will be evaluated using the CAM-ICU scale during ICU stay. The association between perioperative ONSD values and postoperative cognitive outcomes, extubation time, ICU stay, and neurological complications will be analyzed.

Participants needed: 100
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Bursa Yuksek Ihtisas Training and Research HospitalUpdated: Mar 6, 2026Locations: 1Duration: 1 Month
Eligibility criteria

Age between 18 and 80 years [+4]

Age below 18 or above 80 years [+9]

Status: Not yet recruiting

Ultrasound-Based Prediction of Hemodynamic Instability During CVVHDF Initiation

This prospective observational study aims to evaluate the ability of transthoracic echocardiographic and bedside ultrasonographic parameters to predict intradialytic hypotension and hemodynamic instability at the initiation of continuous venovenous hemodiafiltration (CVVHDF) in adult intensive care unit patients.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Bursa Yuksek Ihtisas Training and Research HospitalUpdated: Feb 13, 2026Duration: 1 Year
Eligibility criteria

Adult patients (≥18 years) admitted to the intensive care unit [+3]

Acute coronary syndrome [+5]

Status: Not yet recruiting

Effect of Injection Duration of Fascial Plane Blocks on Block Success

This prospective observational study aims to evaluate the impact of injection duration during fascial plane blocks on block success and analgesic efficacy in patients undergoing laparoscopic cholecystectomy. The hypothesis is that shorter injection durations increase injection pressure, potentially limiting local anesthetic spread, while longer durations facilitate broader anesthetic distribution.

Participants needed: 100
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Bursa Yuksek Ihtisas Training and Research HospitalUpdated: Jul 31, 2025Locations: 1
Eligibility criteria

Laparoscopic cholecystectomy surgery [+1]

Uncontrolled Arterial Hypertension [+6]