[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Sinai University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":190},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,48,73,96,120,140,163],{"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":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100621119","effectiveness-of-electrical-stimulation-and-biofeedback-on-fecal-incontinence-in-children-with-repaired-anorectal-malformation-100621119",false,"NCT07366476","Effectiveness of Electrical Stimulation and Biofeedback on Fecal Incontinence in Children With Repaired Anorectal Malformation","Effectiveness of Electrical Stimulation and Biofeedback on Fecal Incontinence in Children With Repaired Anorectal Malformation: A Comparative Randomized Clinical Trial","Inclusion Criteria:\n\n* children with repaired anorectal malformation\n* evident spared anal sphincter muscles by MRI\n* the age range from 6 to 10 years\n* able to follow instructions\n* Faecal symptoms will be evaluated for a month to confirm study eligibility.\n\nExclusion Criteria:\n\n* children with absent anal sphincter muscles by MRI\n* children with post-colon surgery other than ARM\n* neurologic\u002Fneuropathic disorder\n* sensory or hearing deficits\n* psychological disturbances.","ALL","6 Years","10 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aimed to investigate and compare the effect of electrical stimulation and biofeedback with electrical stimulation alone on fecal incontinence in children with repaired imperforate anus, with ages from 6 to 10 years.",[27,28],"Fecal Incontinence (FI)","Anorectal Malformations",[30,31,32,33,34],"fecal incontinence","anorectal malformation","biofeedback","anal electrical stimulation","pelvic floor muscles training","NOT_YET_RECRUITING","2026-05-05",{"date":38,"type":39},"2026-05-06","ACTUAL",{"date":41,"type":21},"2026-05-01",{"date":43,"type":21},"2026-11-01",{"name":45,"class":46},"Sinai University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":63,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":72},"100606042","effects-of-laser-acupuncture-treatment-in-hypertension-haemodialysis-patients-100606042","NCT07170397","Effects of Laser Acupuncture Treatment in Hypertension Haemodialysis Patients","Effects of a Single Session of Laser Acupuncture Treatment on Blood Pressure and in Hypertension Haemodialysis Patients","Inclusion Criteria:\n\n* sixty hemodialysis patients undergoing physical therapy treatments will participate in the study. Their mean age will range from (18-65) years old\n\nExclusion Criteria:\n\n* a failure to take part in more than three light therapy sessions; a kidney transplant; and death","18 Years","60 Years",{"count":58,"type":21},60,[24],"The purpose of this study is to find the effect of acupuncture laser therapy on Blood Pressure in Hypertension Haemodialysis Patients",[62],"Hypertension",[64],"laser Acupuncture Treatment, Blood Pressure, Hypertension Haemodialysis Patients",{"date":66,"type":39},"2026-05-11",{"date":68,"type":21},"2026-05-30",{"date":70,"type":21},"2026-12-01",{"name":45,"class":46},2,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":80,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":22,"phases":83,"briefSummary":84,"conditions":85,"keywords":88,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":90,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":47},"100604575","phonophoresis-with-bee-venom-evaluating-its-efficacy-in-managing-pain-and-enhancing-mobility-in-knee-osteoarthritis-patients-100604575","NCT07151300","Phonophoresis With Bee Venom: Evaluating Its Efficacy in Managing Pain and Enhancing Mobility in Knee Osteoarthritis Patients","BEE-KNEE","Inclusion Criteria:\n\n* Age 40-75 years\n* Clinically and radiographically confirmed knee osteoarthritis\n* Moderate to severe pain (VAS ≥ 4)\n* Willingness to provide informed consent\n\nExclusion Criteria:\n\n* Allergy to bee products or topical agents used in the study\n* Knee surgery or trauma in the past year\n* Intra-articular injection in the past 6 months\n* Other musculoskeletal or systemic conditions affecting the knees (e.g., rheumatoid arthritis)\n* Pregnancy or contraindication to ultrasound therapy","40 Years","75 Years",{"count":20,"type":21},[24],"Brief Summary:\n\nThis single-blind, randomized controlled trial will investigate the efficacy of bee venom phonophoresis in managing pain and improving mobility in patients with knee osteoarthritis. Thirty adults aged 40-75 years with clinically and radiographically confirmed knee osteoarthritis will be randomly assigned to receive either bee venom phonophoresis or placebo phonophoresis with a neutral gel. Ultrasound parameters will be standardized for all participants.\n\nPrimary outcomes are pain reduction, measured by the Visual Analog Scale (VAS), and functional mobility, assessed by the Timed Up and Go (TUG) test. The secondary outcome is walking endurance, measured by the Six-Minute Walk Test (6MWT). Assessments will be conducted at baseline and post-intervention.\n\nThe study is designed to determine whether bee venom phonophoresis offers greater clinical benefit compared to placebo phonophoresis, potentially providing a non-invasive, adjunctive treatment option for knee osteoarthritis. Ethical approval has been obtained from the Faculty of Physical Therapy, Sinai University, and all participants will provide written informed consent.",[86,87],"Knee Osteoarthritis","Osteoarthritis",[87,89],"Osteoarthritis, Knee",{"date":66,"type":39},{"date":92,"type":21},"2026-05-15",{"date":94,"type":21},"2026-12-25",{"name":45,"class":46},{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":102,"eligibilityCriteria":103,"healthyVolunteers":11,"sex":16,"minAge":55,"maxAge":104,"enrollmentInfo":105,"targetDuration":4,"studyType":22,"phases":106,"briefSummary":107,"conditions":108,"keywords":112,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":116,"startDateStruct":117,"completionDateStruct":118,"leadSponsor":119,"locationsCount":47},"100604576","efficacy-of-bee-venom-phonophoresis-in-treating-chronic-sinusitis-100604576","NCT07151313","Efficacy of Bee Venom Phonophoresis in Treating Chronic Sinusitis:","Efficacy of Bee Venom Phonophoresis in Treating Chronic Sinusitis: A Double-Blind Randomized Controlled Trial","BEE-SONIC","Inclusion Criteria:\n\n* Adults aged 18 to 65 years.\n* Clinical diagnosis of chronic sinusitis (symptoms ≥ 12 weeks) or acute sinusitis confirmed by an otolaryngologist.\n* Willing and able to provide written informed consent.\n\nExclusion Criteria:\n\n* Known allergy or hypersensitivity to bee venom or bee products.\n* Skin conditions (e.g., eczema, dermatitis, open wounds) over the area of ultrasound application.\n* Severe comorbid medical conditions (e.g., uncontrolled asthma, autoimmune disease, malignancy).\n* Pregnancy or breastfeeding.\n* Use of systemic corticosteroids, antibiotics, or other medications that may significantly alter sinusitis symptoms within 4 weeks prior to enrollment.\n* Participation in another clinical trial within the past 30 days.","65 Years",{"count":20,"type":21},[24],"This double-blind, randomized controlled trial (BEE-SONIC) aims to evaluate the efficacy of bee venom phonophoresis in the treatment of chronic sinusitis. Thirty adult patients (aged 18-65 years) with clinically diagnosed chronic or acute sinusitis will be randomized into two groups: the intervention group will receive bee venom phonophoresis using low-to-moderate intensity ultrasound, while the control group will receive standard care consisting of oral decongestants and saline nasal irrigation. Primary outcomes include improvement in symptom severity (SNOT-22, Visual Analog Scale) and quality of life (SF-33). Secondary outcomes include reduction in facial pain, nasal congestion, and patient satisfaction. Data will be collected at baseline, midpoint, and post-intervention, and analyzed using paired t-tests and ANOVA. The study has received ethics approval from Sinai University's Human Research Ethics Committee, and informed consent will be obtained from all participants.",[109,110,111],"Chronic Sinusitis","Acute Sinusitis","Rhinosinusitis",[113,114,115],"Sinusitis","Rhinosinusitis, Chronic","Rhinosinusitis, Acute",{"date":66,"type":39},{"date":92,"type":21},{"date":94,"type":21},{"name":45,"class":46},{"id":121,"slug":122,"hasResults":11,"nctId":123,"briefTitle":124,"officialTitle":125,"acronym":4,"eligibilityCriteria":126,"healthyVolunteers":127,"sex":16,"minAge":4,"maxAge":56,"enrollmentInfo":128,"targetDuration":4,"studyType":22,"phases":129,"briefSummary":130,"conditions":131,"keywords":133,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":135,"startDateStruct":136,"completionDateStruct":137,"leadSponsor":139,"locationsCount":47},"100600581","efficacy-of-of-acupuncture-laser-therapy-on-hemodialysis-patients-100600581","NCT07099352","Efficacy of of Acupuncture Laser Therapy on Hemodialysis Patients","Efficacy of of Acupuncture Laser Therapy on Neck Pain Severity and Quality of Life in Hemodialysis Patients","Inclusion Criteria:\n\n-Their mean age will range from (18-65) years old.\n\nExclusion Criteria:\n\n-a failure to take part in more than three light therapy sessions; a kidney transplant; and death.",true,{"count":58,"type":21},[24],"This expected prospective randomized control trial study will involve 60 haemodialysis patients with neck pain. The patients in the experimental group (E) will subject, medical treatment besides acupuncture laser therapy. Medical treatment will be used in the control group (C). Pain and quality of life assessment will be used in the assessment of outcome.",[132],"Hemodialysis",[134],"Hemodialysis, Acupuncture Laser Therapy",{"date":66,"type":39},{"date":41,"type":21},{"date":138,"type":21},"2026-10-01",{"name":45,"class":46},{"id":141,"slug":142,"hasResults":11,"nctId":143,"briefTitle":144,"officialTitle":145,"acronym":146,"eligibilityCriteria":147,"healthyVolunteers":11,"sex":16,"minAge":55,"maxAge":81,"enrollmentInfo":148,"targetDuration":4,"studyType":22,"phases":150,"briefSummary":151,"conditions":152,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":158,"startDateStruct":159,"completionDateStruct":160,"leadSponsor":162,"locationsCount":4},"100600591","ultrasound-enhanced-propolis-therapy-for-healing-diabetic-foot-wounds-100600591","NCT07099482","\"Ultrasound-Enhanced Propolis Therapy for Healing Diabetic Foot Wounds\"","Effectiveness of Propolis Phonophoresis on Wound Healing in Diabetic Ulcer: a Randomized Controlled Trial","PEARL","Inclusion Criteria:\n\nAdults aged 18 to 75 years\n\nDiagnosed with type 1 or type 2 diabetes mellitus\n\nPresence of a diabetic foot ulcer classified as Grade 1 or 2 (Wagner classification)\n\nUlcer size between 1 cm² and 5 cm²\n\nAble and willing to provide informed consent\n\nExclusion Criteria:\n\nSevere infection or presence of osteomyelitis at the ulcer site\n\nUse of systemic immunosuppressants or corticosteroids\n\nKnown allergy or hypersensitivity to propolis\n\nPregnant or breastfeeding women\n\nParticipation in another clinical trial within the past 30 days",{"count":149,"type":21},80,[24],"This study aims to evaluate whether using ultrasound (phonophoresis) can help deliver propolis-a natural compound made by bees-more effectively into the skin to speed up wound healing in people with diabetic foot ulcers. Diabetic foot ulcers are a common and serious complication of diabetes and often take a long time to heal. Propolis has natural anti-inflammatory and antimicrobial properties that may promote healing, but it does not easily penetrate the skin. By using ultrasound to enhance absorption, this study tests whether combining propolis with phonophoresis is more effective than standard wound care alone. Participants will be randomly assigned to receive either the propolis ultrasound therapy or standard care. The study will measure wound size, healing time, pain, infection rates, and quality of life.",[153,154,155,156,157],"Diabetic Foot Ulcer t","Type 1 Diabetes Mellitus","Type 2 Diabetes Mellitus","Wound Management","Chronic Wound Healing",{"date":38,"type":39},{"date":68,"type":21},{"date":161,"type":21},"2026-09-25",{"name":45,"class":46},{"id":164,"slug":165,"hasResults":11,"nctId":166,"briefTitle":167,"officialTitle":167,"acronym":168,"eligibilityCriteria":169,"healthyVolunteers":11,"sex":16,"minAge":170,"maxAge":171,"enrollmentInfo":172,"targetDuration":173,"studyType":174,"phases":4,"briefSummary":175,"conditions":176,"keywords":178,"overallStatus":181,"whyStopped":4,"lastUpdateSubmitDate":182,"lastUpdatePostDateStruct":183,"startDateStruct":185,"completionDateStruct":187,"leadSponsor":189,"locationsCount":47},"100556894","relationship-between-gross-motor-coordination-and-balance-in-children-with-spastic-cerebral-palsy-100556894","NCT06531044","Relationship Between Gross Motor Coordination and Balance in Children With Spastic Cerebral Palsy","CP","Inclusion Criteria:\n\n1. They were scored Level I on the Gross Motor Function Classification System (GMFCS).\n2. The subjects' age was from five to eleven years.\n3. They were at least 1-meter-tall and not less 20 Kg.\n4. They had to comprehend verbal commands.\n5. They were score 1 to 1+ based on Modified Ashworth' Scale.\n\nExclusion Criteria:\n\n1. Contracture, deformity and\u002For tightness in upper or lower limbs.\n2. Botulinum toxin in the last year.\n3. Recent fracture.\n4. Vertigo or dizziness.\n5. Epilepsy.\n6. Osteoporosis.\n7. Recent operation in the six months at least (according to the type of operation).","5 Years","11 Years",{"count":58,"type":21},"1 Day","OBSERVATIONAL","This study aims to determine if there is a connection between gross motor coordination and balance in children with spastic cerebral palsy. Since these children often struggle with balance and other motor skills, researchers hypothesize that there is no link between the two abilities.",[177],"Cerebral Palsy",[177,179,180],"Balance","Gross Motor Coordination","RECRUITING","2024-07-28",{"date":184,"type":39},"2024-07-31",{"date":186,"type":39},"2024-03-06",{"date":188,"type":21},"2024-11-20",{"name":45,"class":46},""]