[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100629095":3},{"organization":4,"armGroups":7,"interventions":29,"overallOfficials":48,"centralContacts":49,"locations":57,"responsibleParty":76,"collaborators":48,"id":78,"slug":79,"hasResults":80,"nctId":81,"briefTitle":82,"officialTitle":82,"acronym":48,"eligibilityCriteria":83,"healthyVolunteers":80,"sex":84,"minAge":85,"maxAge":86,"enrollmentInfo":87,"targetDuration":48,"studyType":90,"phases":91,"briefSummary":93,"conditions":94,"keywords":48,"overallStatus":60,"whyStopped":48,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":105},{"fullName":5,"class":6},"Sehat Medical Complex","OTHER",[8,14,19,23],{"label":9,"type":10,"description":11,"interventionNames":12},"Group A (Blood Flow Restriction Therapy)","EXPERIMENTAL","4 Sets of exercise with restriction cuff 30,15,15,15 with cable system pulley",[13],"Other: Blood flow Restriction therapy",{"label":15,"type":10,"description":16,"interventionNames":17},"Group B (Extracorporeal Shock wave therapy)","10 minutes shocks of 2000 J\u002Fsession",[18],"Device: ESWT",{"label":20,"type":10,"description":21,"interventionNames":22},"Group C (Combination of BFRT+ESWT)","Interventional study group Combination therapy",[13,18],{"label":24,"type":25,"description":26,"interventionNames":27},"Control Group D","SHAM_COMPARATOR","Control group with routine physical therapy",[28],"Other: Control",[30,37,42],{"type":6,"name":31,"description":32,"armGroupLabels":33,"otherNames":34},"Blood flow Restriction therapy","BFRT 4 Sets of exercise with restriction cuff 30,15,15,15 with cable system pulley ESWT 10 minutes shocks of 2000 J\u002Fsession",[9,20],[35,36],"BFRT","ESWT",{"type":38,"name":36,"description":16,"armGroupLabels":39,"otherNames":40},"DEVICE",[15,20],[41],"Shock wave therapy",{"type":6,"name":43,"description":44,"armGroupLabels":45,"otherNames":46},"Control","Electric heating pad (Besmed, Taiwan) 10 minutes, TENS (Comfy Stim, Taiwan Model #: EV-806) 10 minutes",[24],[47],"Routine physical therapy",null,[50,55],{"name":51,"role":52,"phone":53,"phoneExt":48,"email":54},"imran Ghafoor, M Phil","CONTACT","+923344292887","imran.ghafoor64@gmail.com",{"name":56,"role":52,"phone":48,"phoneExt":48,"email":48},"Sahar Ijaz, PhD Anatomy",[58],{"facility":59,"status":60,"city":61,"state":62,"zip":63,"country":64,"countryCode":65,"cosmosGeoPoint":66,"geoPoint":71,"contacts":72},"Sehat Medical Complex\u002FUOL\u002FUVAS","RECRUITING","Lahore","Punjab Province","54000","Pakistan","PK",{"type":67,"coordinates":68},"Point",[69,70],74.35071,31.558,{"lat":70,"lon":69},[73],{"name":74,"role":52,"phone":75,"phoneExt":48,"email":54},"Imran Ghafoor","03344292887",{"type":77,"investigatorFullName":48,"investigatorTitle":48,"investigatorAffiliation":48,"oldNameTitle":48,"oldOrganization":48},"SPONSOR","100629095","anatomical-evaluation-of-supraspinatus-through-ultrasonography-and-biomechanical-measurements-following-different-combinations-of-physical-therapies-in-patients-of-supraspinatus-tendinitis-100629095",false,"NCT07470190","Anatomical Evaluation of Supraspinatus Through Ultrasonography and Biomechanical Measurements Following Different Combinations of Physical Therapies in Patients of Supraspinatus Tendinitis","Inclusion Criteria:\n\n* unilateral shoulder pain\n* both gender group\n* two positive tests of (Neer impingement test, Hawkins-Kendy test, Empty can test),\n* shoulder pain history up to 3 months\n* not receiving any physiotherapy last 3 months.\n* not receiving pain medications (NSAIDS) for last 15 days.\n\nExclusion Criteria:\n\n* referred shoulder pain\n* limited shoulder ROM less then 90 degree\n* previous shoulder surgery, intra articular injection or nerve block last 6 months.\n* patient with 180 mmHg blood pressure\u002Funcontrolled BP\n* upper limb fracture, uncontrolled diabetes, open wounds, fistula and vascular surgery.\n* pregnant woman or 6 month history of pregnancy","ALL","40 Years","60 Years",{"count":88,"type":89},60,"ESTIMATED","INTERVENTIONAL",[92],"NA","A randomized controlled trial will be conducted to get the expected outcomes. Patients of both gender groups with unilateral shoulder pain will be selected with age range 40-60 years from Sehat medical complex and randomly allocated into four groups (Group A, B, C and D) of two different trials (Trial I and Trial II). The sample size will be 120 patients for both trials. Musculoskeletal ultrasound, goniometry, pain pressure threshold, dynamometer and functional indices will be used to measure the tendon thickness, range of motion, pain, muscle strength and function level. The group A will get BFRT, Group B will get ESWT, group c will get the combination of both and group D will be the Control group (Routine physical therapy). In Trial II the group A will get BFRT, Group B will get Eccentric Training, Group C will get combination of both A \\& B and group D will be control group. data will be collected at baseline, 4th week, 8th week and 12 week of interventions. For data analysis SPSS version 25 will be used. Repeated measures ANOVA will be applied to compare the quantitative data within and between the groups. Post-Hoc test Tukey and Bonferroni correction will be used. The level of significance will be set at 5% (P\\\u003C0.05).",[95],"Supraspinatus Tendinitis","2026-03-09",{"date":98,"type":99},"2026-03-13","ACTUAL",{"date":101,"type":99},"2026-02-23",{"date":103,"type":89},"2026-08-30",{"name":5,"class":6},1]