[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"MTI University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":231},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,42,68,93,120,140,175,207],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100641171","efficacy-of-diclofenac-sodium-shock-wave-phonophoresis-on-patients-with-subacromial-impingement-syndrome-100641171",false,"NCT07657637","Efficacy of Diclofenac Sodium Shock Wave Phonophoresis on Patients With Subacromial Impingement Syndrome","Efficacy of Diclofenac Sodium Shock Wave Phonophoresis on Patients With Subacromial Impingement Syndrome: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients age range between 25-40 years ago.\n* Shoulder pain between 60- 120° with shoulder elevation (positive painful arch test).\n* Grade 2 impingement syndrome according to neer classification.\n\nExclusion Criteria:\n\n* Shoulder affected bilaterally\n* Receiving anesthetic or corticosteroid injections within 4 weeks of study enrollment\n* Surgery or previous fractures of the ipsilateral humeral head of the affected shoulder\n* Osteoarthritis in the acromioclavicular or glenohumeral joints","ALL","25 Years","40 Years",{"count":20,"type":21},70,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of the study is to determine the effect of radial shock wave Phonophoresis on patients with impingement syndromes. to answer the following questions:\n\ndoes shock wave Phonophoresis have and effect on pain? does shock wave Phonophoresis have and effect on shoulder function? does shock wave Phonophoresis have and effect on subacromial space? patients will be randomized to two groups: Group (A): patients will receive shock wave Phonophoresis plus conventional physical therapy.\n\nGroup (B): Patients will receive shock wave plus conventional Physical therapy.",[27,28],"Shock Wave","Subacromial Impingement Syndrome","NOT_YET_RECRUITING","2026-06-14",{"date":32,"type":33},"2026-06-18","ACTUAL",{"date":35,"type":21},"2026-06-30",{"date":37,"type":21},"2026-10-30",{"name":39,"class":40},"MTI University","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":16,"minAge":49,"maxAge":50,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":54,"conditions":55,"keywords":57,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":41},"100642814","a-study-comparing-the-hall-technique-and-conventional-stainless-steel-crowns-in-carious-primary-molars--clinical-outcomes-anxiety-time-and-cost-effectiveness-100642814","NCT07648654","A Study Comparing the Hall Technique and Conventional Stainless-Steel Crowns in Carious Primary Molars : Clinical Outcomes, Anxiety, Time, and Cost-Effectiveness","A Randomized Controlled Trial Comparing the Hall Technique and Conventional Stainless-Steel Crowns in Carious Primary Molars : Clinical Outcomes, Anxiety, Time, and Cost-Effectiveness","Inclusion Criteria:\n\n* Only patients aged between 5-8 years old will be included in the study. The following criteria is used to determine eligibility to be part of the study:\n\nOnly participants with one or two asymptomatic, vital primary molars following completion of treatment, will be able to participate in the clinical study .The posterior teeth may have multi-surface caries within the proximal and occlusal surfaces of the teeth, either one or both surfaces have been involved with caries and results in complete coronal coverage of the tooth.\n\nThe posterior teeth included must show evidence of caries on x-rays (ICDAS 0-3), but with no evidence of pulp involvement\u002Fradicular pathology.\n\nAll included teeth must be able to be restored and possess sufficient structure for retention of a preformed metal crown (PMC).\n\nParticipants will be eligible if they demonstrate cooperation (i.e. Frankl behaviour rating 3-4) during examination\u002Fanesthesia\u002Fsurgery.\n\nExclusion Criteria:\n\n* o Any clinical symptoms or signs associated with pulpal pathology which could include sinus tract, spontaneous pain, tenderness to percussion or pathological mobility.\n\n  * Radiographic evidence of pulp involvement, furcation radiolucency or pathological root resorption exceeding one-third (1\u002F3) of the root length were also considered.\n  * There are certain medical or systemic conditions\u002Fcontra-indicators for routine dental treatment.\n  * Target teeth which have been previously restored have additional requirements.\n  * A follow-up appointment cannot occur because the parent\u002Fguardian will not be able to bring the child in for any follow-up appointments is another issue.","5 Years","8 Years",{"count":52,"type":21},200,[24],"Tooth decay is a widely experienced condition associated with the oral health of children, particularly in posterior teeth. This is attributed to their intricate texture which is commonly encountered during the oral hygiene measures . Caring for posterior teeth affected by tooth decay in children is vital to ensure stability in tooth occlusion, minimizing pain, preventing infections, and facilitating mastication and communication. However, the success of tooth restorations is questionable, particularly due to secondary decay, fracture, loss of retention, and marginal problems.\n\nStainless steel crowns are deemed one of the most durable and reliable treatment options in pediatric dentistry, especially for multi-surface lesions or structurally damaged molars. In a conventional approach to placing SSCs, caries needs to be removed, teeth prepared, and in most cases, local anesthesia is administered. These approaches can be quite time-consuming and may exacerbate dental anxiety in children who report previous negative dental experiences.\n\nIn the last couple of decades, there has been a gradual move toward minimal invasive dentistry (MID) in caries management. This philosophy emphasizes the importance of maintaining sound tooth structure and adopts biological methods instead of traditional operative methods . This is further consolidated by consensus guidelines that recommend either non- selective or selective caries removal methods for the purpose of minimizing patient discomfort and limiting the invasiveness of treatment. Moreover, practitioners highlight the need for early intervention and the application of less invasive methods where clinically indicated.\n\nHT represents a biologically based, minimally invasive approach within the MID framework. This approach involves cementing a preformed metal crown over a carious posterior tooth without local anesthesia, caries excavation, or tooth preparation to seal the lesion from the oral environment. Despite several studies demonstrating favorable results of HT, there is still a lack of well-documented evidence on RCTs comparing clinical and radiographic outcomes, patient anxiety, treatment duration, and cost-effectiveness between HT and conventional SSC placement.\n\nThe aim of the study, therefore, was to establish whether the Hall Technique, compared to the conventional stainless-steel crown technique, is efficient in managing carious posterior teeth in children aged 5-8 years. Outcomes included crown survival, anxiety levels of the patient, treatment time required, and cost-effectiveness over a period of 3 months.",[56],"Hall Technique",[58],"Hall Technique, Stainless-steel crowns, Preformed metal crowns, Dental anxiety.","RECRUITING","2026-06-12",{"date":62,"type":33},"2026-06-15",{"date":64,"type":33},"2026-05-25",{"date":66,"type":21},"2026-08-25",{"name":39,"class":40},{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":74,"eligibilityCriteria":75,"healthyVolunteers":11,"sex":16,"minAge":76,"maxAge":50,"enrollmentInfo":77,"targetDuration":4,"studyType":22,"phases":79,"briefSummary":80,"conditions":81,"keywords":84,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":89,"completionDateStruct":90,"leadSponsor":92,"locationsCount":4},"100641766","aquatic-therapy-versus-sensory-room-intervention-for-sensory-motor-function-in-children-with-sensory-processing-disorder-100641766","NCT07646951","Aquatic Therapy Versus Sensory Room Intervention for Sensory-Motor Function in Children With Sensory Processing Disorder","Comparative Impact of Aquatic Therapy and Conventional Sensory Room Intervention on Adaptive Neural Responses and Sensory-Motor Praxis in Children With Monochannel Sensory Processing Disorder: A Randomized Clinical Trial","AQUA vs SRI Tr","Inclusion Criteria:\n\n* Children aged 4-8 years with a confirmed diagnosis of monochannel sensory processing disorder.\n\nExclusion Criteria:\n\n* Medical Instability: Any acute illness, fever, or infectious diseases (e.g., ear infections or open wounds) that contraindicate pool therapy.\n* Neurological Risks: Children with uncontrolled seizures or epilepsy that poses a safety risk in an aquatic environment.\n* Severe Phobia: Extreme fear of water (hydrophobia) that prevents active participation in aquatic exercises.\n* Recent Surgery: Any recent surgical interventions (orthopedic or neurological) that have not yet reached full clinical clearance for physical activity.\n* Incontinence: Severe lack of bowel or bladder control unless specific medical swim diapers are utilized according to facility policy.","4 Years",{"count":78,"type":21},60,[24],"This randomized clinical trial compares the effects of aquatic therapy and conventional sensory room intervention on adaptive neural responses and sensory-motor praxis in children with Monochannel Sensory Processing Disorder. Participants will be randomly assigned to one of the two intervention groups. Outcomes related to sensory processing, sensory-motor praxis, and adaptive responses will be evaluated before and after treatment. The study aims to determine whether aquatic therapy provides additional benefits compared with conventional sensory room intervention in improving sensory integration and functional performance in affected children.",[82,83],"Neuro Developmental Delay","Sensory Disorders",[85,86],"Aquatic Therapy vs Sensory Room + SPD + Children","sensory disorder - aquatic therapy","2026-06-09",{"date":62,"type":33},{"date":62,"type":21},{"date":91,"type":21},"2026-12-20",{"name":39,"class":40},{"id":94,"slug":95,"hasResults":11,"nctId":96,"briefTitle":97,"officialTitle":97,"acronym":98,"eligibilityCriteria":99,"healthyVolunteers":100,"sex":101,"minAge":102,"maxAge":103,"enrollmentInfo":104,"targetDuration":4,"studyType":22,"phases":106,"briefSummary":107,"conditions":108,"keywords":110,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":112,"lastUpdatePostDateStruct":113,"startDateStruct":115,"completionDateStruct":117,"leadSponsor":119,"locationsCount":41},"100638945","the-impact-of-whole-body-vibration-and-relaxation-techniques-on-adolescent-athlete-girls-with-triad-syndrome-100638945","NCT07587346","The Impact of Whole-Body Vibration and Relaxation Techniques on Adolescent Athlete Girls With Triad Syndrome\"","WBV for triad","Inclusion Criteria:\n\n* Low energy availability (with or without disordered eating)\n* Menstrual dysfunction (oligomenorrhea)\n* Low bone mineral density or a history of stress fractures\n\nExclusion criteria:\n\n* Recent fractures or unhealed stress fractures within the last 6 months.\n* Presence of serious medical conditions that contraindicate WBV or exercise participation, such as: Uncontrolled cardiovascular disease, Uncontrolled hypertension, Neurological disorders, Severe vestibular disorders, Active cancer, Bleeding\u002Fclotting disorders.\n* Severe eating disorder requiring inpatient medical or psychiatric treatment.\n* Current use of medications that significantly affect bone or hormonal status\n* Participation in another interventional clinical study within the last 3 months.\n* Inability or unwillingness to provide assent\u002Fconsent or comply with study procedures.",true,"FEMALE","14 Years","16 Years",{"count":105,"type":21},50,[24],"This study aims to explore the effects of Whole-Body Vibration (WBV) exercises and relaxation techniques on adolescent female athletes who are experiencing Female Athlete Triad Syndrome - a condition that may include low bone density, irregular menstrual cycles, and low energy availability.\n\nParticipants will take part in a structured program combining vibration training and relaxation sessions over several weeks. The goal is to determine whether this combination can improve bone health, menstrual regularity, physical performance, and overall well-being in young female athletes.",[109],"Menstrual Cycle Abnormal",[111],"Athelte traid , whole body vibration , relaxation technique","2026-05-08",{"date":114,"type":33},"2026-05-14",{"date":116,"type":33},"2025-11-02",{"date":118,"type":21},"2026-05-22",{"name":39,"class":40},{"id":121,"slug":122,"hasResults":11,"nctId":123,"briefTitle":124,"officialTitle":124,"acronym":4,"eligibilityCriteria":125,"healthyVolunteers":100,"sex":101,"minAge":126,"maxAge":18,"enrollmentInfo":127,"targetDuration":4,"studyType":22,"phases":128,"briefSummary":129,"conditions":130,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":132,"lastUpdatePostDateStruct":133,"startDateStruct":135,"completionDateStruct":137,"leadSponsor":139,"locationsCount":4},"100636984","effect-of-electroacupuncture-on-bowel-function-and-quality-of-life-in-postpartum-constipation-a-randomized-controlled-trial-100636984","NCT07572786","Effect of Electroacupuncture on Bowel Function and Quality of Life in Postpartum Constipation: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Females aged 20-40 years\n* Within 6 weeks postpartum\n* Diagnosed with constipation\n* Willing to participate\n\nExclusion Criteria:\n\n* History of gastrointestinal disorders\n* Previous colorectal surgery\n* Neurological diseases affecting bowel function\n* Contraindications to acupuncture (tumor, scar or keloids \\& spinal instability ).","20 Years",{"count":78,"type":21},[24],"Postpartum constipation is a common condition affecting women after childbirth, leading to discomfort and reduced quality of life. Pharmacological treatments may have side effects and are sometimes avoided during breastfeeding. Electroacupuncture is a safe, non-pharmacological intervention that may improve bowel motility. However, limited evidence exists regarding its effectiveness in postpartum women, necessitating further investigation",[131],"Postpartum Constipation","2026-05-01",{"date":134,"type":33},"2026-05-07",{"date":136,"type":21},"2026-05-20",{"date":138,"type":21},"2026-10-20",{"name":39,"class":40},{"id":141,"slug":142,"hasResults":11,"nctId":143,"briefTitle":144,"officialTitle":145,"acronym":146,"eligibilityCriteria":147,"healthyVolunteers":11,"sex":16,"minAge":148,"maxAge":149,"enrollmentInfo":150,"targetDuration":4,"studyType":22,"phases":152,"briefSummary":153,"conditions":154,"keywords":158,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":168,"startDateStruct":170,"completionDateStruct":172,"leadSponsor":174,"locationsCount":41},"100608084","effect-of-electromagnetic-field-therapy-on-balance-and-gait-in-paraparetic-patients-100608084","NCT07196956","Effect of Electromagnetic Field Therapy on Balance and Gait in Paraparetic Patients","The Role of Electromagnetic Field Therapy in Improving Perturbation of Balance and Gait Disorders in Paraparetic Patients","EMT-BG","Inclusion Criteria:\n\n* Diagnosis of paraparesis with spinal cord lesion level between T6 and T12. Age between 25 and 45 years. Muscle spasticity graded as II or III on the Modified Ashworth Scale (MAS) for hip adductors and ankle plantar flexors.\n\nMedically and psychologically stable. Conscious and cooperative, able to follow instructions. Able to provide informed consent.\n\nExclusion Criteria:\n\n* Presence of metal implants or pacemakers (contraindicated for electromagnetic therapy).\n\nHistory of seizures or epilepsy. Active malignancy or infection. Severe cognitive or psychiatric impairment that would interfere with participation.\n\nUse of alcohol or recreational drugs during the study period. Participation in another concurrent physical or electromagnetic therapy trial. Unstable medical condition (e.g., uncontrolled hypertension, cardiovascular disease).","15 Years","45 Years",{"count":151,"type":21},30,[24],"This study will investigate whether adding electromagnetic field therapy (EMT) to a standard physical therapy program is more effective than physical therapy alone for improving balance and walking ability in paraparetic patients.\n\nThirty patients with paraparesis (weakness in the lower limbs) due to spinal cord lesions between levels T6 and T12 will be randomly assigned to one of two groups. Both groups will receive a 45-minute physical therapy session, three times per week for two months. The physical therapy program will include stretching, strengthening, balance, and gait training exercises.\n\nThe key difference will be that one group (Group II) will also receive active low-frequency (0.5 Hz) electromagnetic therapy applied to their spine during their sessions, while the other group (Group I) will receive a placebo (inactive) EMT device.\n\nPatients will be assessed before and after the 2-month treatment period. The assessments will measure muscle spasticity (using the Modified Ashworth Scale), balance (using the Biodex Balance System), and detailed gait parameters like step length, stride length, and base of support (using a 3D motion analysis system",[155,156,157],"Paraparesis","Gait Disorders, Neurologic","Postural Balance Disorders",[159,160,161,162,163,164,165,166],"Electromagnetic Field Therapy","Electromagnetic Stimulation","Physical Therapy Modalities","Spasticity","Rehabilitation","Biodex Balance System","Motion Analysis","Modified Ashworth Scale","2026-01-01",{"date":169,"type":33},"2026-01-05",{"date":171,"type":21},"2026-01-11",{"date":173,"type":21},"2026-03-01",{"name":39,"class":40},{"id":176,"slug":177,"hasResults":11,"nctId":178,"briefTitle":179,"officialTitle":180,"acronym":181,"eligibilityCriteria":182,"healthyVolunteers":11,"sex":16,"minAge":149,"maxAge":183,"enrollmentInfo":184,"targetDuration":4,"studyType":22,"phases":185,"briefSummary":186,"conditions":187,"keywords":191,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":199,"lastUpdatePostDateStruct":200,"startDateStruct":202,"completionDateStruct":204,"leadSponsor":206,"locationsCount":4},"100618686","anterior-foot-wedge-with-neuromuscular-training-for-balance-in-parkinsons-disease-100618686","NCT07334847","Anterior Foot Wedge With Neuromuscular Training for Balance in Parkinson's Disease","Efficacy of Anterior Foot Wedge Modulation With Neuromuscular Training on Balance During Walking in Parkinsonian Patients","AFW-NT","Inclusion Criteria:\n\n* Diagnosis of Parkinson's disease, confirmed by neurologist. Disease severity classified as Stage III on the Hoehn \\& Yahr scale. Age between 45 and 75 years. Medically stable (normal vital signs). Conscious, cooperative, and able to follow instructions. No severe cognitive or psychological impairment. Able to provide informed consent.\n\nExclusion Criteria:\n\n* Severe disability or advanced Parkinsonism (Stage IV or V). Presence of other neurological or orthopedic conditions affecting gait or balance (e.g., stroke, spinal cord injury, severe arthritis).\n\nHistory of diabetes in second-degree relatives (as specified in your protocol). Unstable medical conditions (e.g., uncontrolled hypertension, cardiac disease). Inability to stand or walk with minimal assistance. Non-cooperative or unable to tolerate assessment procedures (EMG, Biodex, motion analysis).","75 Years",{"count":151,"type":21},[24],"This study will test whether combining an anterior foot wedge with neuromuscular training can improve balance, gait, and muscle activity in people with Parkinson's disease. Thirty patients (ages 45-75) with moderate Parkinson's (Hoehn \\& Yahr Stage III) will be randomly assigned to one of two groups:\n\nGroup 1 (Control): Receives a standard physical therapy program including stretching, strengthening, PNF, weight-shifting, and gait training.\n\nGroup 2 (Experimental): Receives the same physical therapy plus neuromuscular training using the Biodex Multi-Joint System and a custom anterior foot wedge.\n\nAll participants will train for 60 minutes, three times per week, for 8 weeks. Before and after the program, researchers will measure: balance (using the Biodex Balance System), gait (via Unified Parkinson's Disease Rating Scale and motion analysis), and muscle activity in the trunk (using electromyography). The goal is to find a more effective rehabilitation approach to reduce fall risk and improve walking in Parkinson's patients.",[188,189,190],"Parkinson's Disease","Postural Instability","Gait Disorder",[192,193,194,195,196,197,198],"Anterior foot wedge","Neuromuscular training","Balance","Gait","Biodex","Electromyography","Postural stability","2025-12-31",{"date":201,"type":33},"2026-01-12",{"date":203,"type":21},"2026-01-02",{"date":205,"type":21},"2026-03-14",{"name":39,"class":40},{"id":208,"slug":209,"hasResults":11,"nctId":210,"briefTitle":211,"officialTitle":212,"acronym":4,"eligibilityCriteria":213,"healthyVolunteers":11,"sex":16,"minAge":18,"maxAge":214,"enrollmentInfo":215,"targetDuration":4,"studyType":22,"phases":217,"briefSummary":218,"conditions":219,"keywords":221,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":223,"lastUpdatePostDateStruct":224,"startDateStruct":226,"completionDateStruct":228,"leadSponsor":230,"locationsCount":4},"100570571","effect-of-insulin-therapy-by-ultrasonography-in-wound-healing-of-chronic-diabetic-patients-100570571","NCT06708975","Effect of Insulin Therapy by Ultrasonography in Wound Healing of Chronic Diabetic Patients","Effect of Transdermal Insulin Therapy by Ultrasonographic in Wound Healing of Chronic Diabetic Patients","Inclusion Criteria:\n\n* patients will be included if they are free from any pathological condition like limb infection, local or proximate malignancy, and anti-coagulated patients.\n\nExclusion Criteria:\n\npatients will be excluded if they have any pathological condition like limb infection, local or proximate malignancy, and anti-coagulated patients.","65 Years",{"count":216,"type":21},40,[24],"The main aim of the study is to determine the effect of transdermal application of insulin therapy by phonophoresis in wound healing in diabetic patients the main question of the study: is insulin phonophoresis is effective in accelerating healing in patients with diabetes mellites? 40 patients will be randomly assigned to two groups group A will receive insulin phonophoresis plus hyper polarized laser therapy and standard wound cleaning and dressing three times weekly over four weeks.\n\nGroup B will receive hyper polarized laser therapy and standard wound cleaning and dressing three times weekly over four weeks.",[220],"Diabetes Mellitus",[222],"diabetes mellites, Insulin Phonophoresis","2024-11-25",{"date":225,"type":33},"2024-11-29",{"date":227,"type":21},"2024-12",{"date":229,"type":21},"2025-02",{"name":39,"class":40},""]