[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"elbow-pain\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:elbow-pain":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,76],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100638108","comparative-effects-of-mulligan-mobilization-with-and-without-myofascial-release-technique-in-management-of-post-traumatic-elbow-stiffness-100638108",false,"NCT07598526","Comparative Effects of Mulligan Mobilization With and Without Myofascial Release Technique in Management of Post Traumatic Elbow Stiffness","Inclusion Criteria:\n\n* Participants aged between 17 and 44 years will be included in the study (Sun et al., 2025).\n* Both male and female patients experiencing mild to moderate elbow pain (3\u002F10 to 5\u002F10 on NPRS) along with restricted range of motion will be eligible (Zulfqar et al., 2021).\n* Subjects having elbow movement limitation of more than 30° in extension, flexion less than 120°, and 50° restriction in both pronation and supination will be included (Masci et al., 2020).\n* Participants will be recruited 3 to 6 weeks after POP removal, and radiographic confirmation of bone\u002Fskeletal healing will be ensured before inclusion (Morrey et al., 2017).\n* Patients with both intra-articular and extra-articular fractures will be considered eligible.\n* Individuals with DASH scores ranging from 45 to 50 points will be included.\n* Only patients willing to participate in the study will be enrolled.\n\nExclusion Criteria:\n\n* Patients with a history of previous surgical excision will be excluded from the study (Zheng et al., 2018).\n* Participants presenting with pathological fractures will not be included (Zulfqar et al., 2021).\n* Patients in the acute stage of fracture will be excluded from participation (Zulfqar et al., 2021).\n* Individuals with metabolic or malignant conditions causing elbow stiffness, such as gout or osteosarcoma, will not be eligible (Fusaro et al., 2014).\n* Patients with elbow fractures associated with a history of metal implants will be excluded (Zheng et al., 2018).\n* Individuals who have already received physiotherapy treatment or medication for the condition will not be included.\n* Patients diagnosed with psychological illnesses that may interfere with following instructions will be excluded.\n* Participants with brain trauma or referred neurological symptoms, including numbness, dizziness, or hyperesthesia, will not be considered (Fusaro et al., 2014).\n* Patients with structural or postural abnormalities involving the shoulder or wrist will be excluded.\n* Individuals with open skin wounds or burn injuries around the affected area will not be included.\n* Patients with a pre-operative history of arthritis will also be excluded from the study.","ALL","17 Years","44 Years",{"count":19,"type":20},30,"ESTIMATED","INTERVENTIONAL",[23],"NA","The Randomize Clinical Trial will involve 30 participants with post traumatic elbow stiffness recruited from Madinah Teaching Hospital and Chiniot General hospital Faisalabad. Consecutive sampling technique will be used. Study will include individuals with \\>30° extension loss and \\\u003C120° flexion, 50° in both directions for pronation-supination, who are 3-6 weeks post-POP removal from radiograph confirmation of skeletal\u002Fbone healing will be insured, who have elbow pain from 3 to 5\u002F10 on NPRS and have fully healed fractures. Both intra-articular and extra-articular injuries will be accepted. DASH Score with 45 to 50 points. Study will exclude pathological or acute fractures, burns, brain trauma, neurological or psychological disorders, history of pre-operative osteoarthritis. Consent will be taken written and verbal from participants before including into study. Patients will be allocated with online randomization generator method into 2 groups. Group A will receive Mulligan Mobilization with Myofascial release technique, while Group B will receive Mulligan Mobilization alone. Hot pack for 20 minutes before treatment and static stretching after treatment will apply in both groups. Each stretch is performed 10 repetition with hold duration of 30 sec and rest period 15 sec between each stretch. Total 3 sessions per week for 4 weeks (12 sessions) on alternative days will be given. Outcome of study will be elbow pain, elbow range of motion (flexion and extension) and functional disability will be measure by using Numerical Pain Rating Scale, Universal Goniometer and Dash Questionnaire Score respectively. Data will be investigated by using SPSS version 2023.",[26,27],"Elbow Stiffness","Elbow Pain",[29,30,31,32,33],"Post op elbow stiffness","Mulligan Mobilization","Myofascial Release Technique","Disabilities of Arm, Shoulder, and Hand","Elbow pain","NOT_YET_RECRUITING","2026-05-13",{"date":37,"type":38},"2026-05-20","ACTUAL",{"date":37,"type":20},{"date":41,"type":20},"2026-09-20",{"name":43,"class":44},"University of Faisalabad","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":15,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":21,"phases":57,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"100544829","phase-4-nonnarcotic-pain-control-in-percutaneous-needle-tenotomy-of-elbow-100544829","NCT06373978","NonNarcotic Pain Control in Percutaneous Needle Tenotomy of Elbow","A Randomized Controlled Trial: Alternative Post Procedural Analgesia With NSAIDs vs Opioids in Percutaneous Needle Tenotomy of Elbow","Inclusion Criteria:\n\n* Provision of signed and dated informed consent form\n* Stated willingness to comply with all study procedures and availability for the duration of the study\n* Male or female, aged 18-65 years\n* Percutaneous Needle Tenotomy of Lateral Elbow Procedure\n* Ability to take oral medication and willingness to participate in a 2-week follow-up pill counts\n* Musculoskeletal ultrasound or MRI with diagnosis of tendinosis of the common extensor tendon of the elbow\n\nExclusion Criteria:\n\n* • Any full thickness common extensor tendon tear of the elbow\n\n  * Prior history of elbow surgery\n  * Symptomatic cervical radiculopathy\n  * Concurrent symptoms of the medial elbow\n  * Treatment with another investigational drug or other intervention concurrently or previously that would interfere with postoperative pain control\n  * Psychiatric illness that impedes evaluation of pain and\u002For narcotics use\n  * No history of inflammatory arthritis, diabetes, chronic regional pain syndrome, connective tissue disease, fibromyalgia or autoimmune disease\n  * No contraindications to NSAIDs or Opioids","18 Years","65 Years",{"count":56,"type":20},92,[58],"PHASE4","This study is a double-blind, randomized controlled trial comparing the effectiveness of oral acetaminophen, diclofenac, and tramadol in reducing the consumption of narcotic doses (primary outcome) and minimizing patients' exposure to narcotics (secondary outcome) following an ultrasound-guided percutaneous needle tenotomy procedure on the lateral elbow.",[27,61],"Chronic Pain",[63,64],"TenJet","Elbow","RECRUITING","2026-02-11",{"date":68,"type":38},"2026-02-13",{"date":70,"type":38},"2024-08-12",{"date":72,"type":20},"2026-06-30",{"name":74,"class":44},"The Cleveland Clinic",2,{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":83,"sex":15,"minAge":4,"maxAge":53,"enrollmentInfo":84,"targetDuration":4,"studyType":21,"phases":86,"briefSummary":87,"conditions":88,"keywords":95,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":108,"lastUpdatePostDateStruct":109,"startDateStruct":111,"completionDateStruct":113,"leadSponsor":115,"locationsCount":45},"100609243","the-utilization-of-ultrasound-to-diagnose-pediatric-elbow-fractures-100609243","NCT07212036","The Utilization of Ultrasound to Diagnose Pediatric Elbow Fractures","The Utilization of Ultrasound to Diagnose Pediatric Elbow Fractures: Evaluation of Cost Savings, Radiation Exposure, and Patient Satisfaction","Inclusion Criteria:\n\n• Pediatric patient with elbow pain\n\nExclusion Criteria:\n\n* Polytrauma (more than one injury)\n* Deformity of the arm including the elbow\n* Pain in any other location than the elbow\n* Pain in other parts of the same limb including the, wrist, forearm, shoulder, hand\n* Pain in other limbs,\n* Puckering of the skin (skin indentation)\n* Obvious fracture\n* Open wound at or around the elbow\n* Pain and swelling without trauma\n* Concerns for tumor or infection\n* Suspected nursemaid's elbow",true,{"count":85,"type":20},225,[23],"The goal of this intervention trial is to learn if a ultrasound diagnosis of elbow fractures can improve care in pediatric patients seen in the emergency room. The main questions it aims to answer are:\n\nThe primary outcomes measured are cost of the emergency visit, radiation exposure, time spent in the emergency department and patient satisfaction.\n\nPatients who are evaluated with ultrasounds of the elbow will be compared to patients who have x-rays of the elbow.\n\nParticipants will be assigned either to the ultrasound group or x-rays group when they present with elbow pain.",[27,89,90,91,92,93,94],"Supracondylar Humerus Fracture","Radial Head Fractures","Radial Head or Neck Fractures","Elbow Dislocation","Humerus Fractures","Jakob II Classification",[96,97,98,99,100,101,102,103,104,105,106,107],"elbow pain","elbow fracture","supracondylar humerus fracture","pediatric","lateral humeral condyle fracture","radial head fracture","radial neck fracture","monteggia fracture","elbow dislocation","radial head dislocation","emergency department","ultrasound","2026-01-27",{"date":110,"type":38},"2026-01-29",{"date":112,"type":38},"2025-07-22",{"date":114,"type":20},"2027-09-02",{"name":116,"class":44},"Nemours Children's Clinic"]