[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hip-pain\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hip-pain":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,50,78,114,136],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100638799","enhancing-exercise-adherence-among-patients-with-lateral-hip-pain-100638799",false,"NCT07597343","Enhancing Exercise Adherence Among Patients With Lateral Hip Pain","The 'As Soon As Possible (ASAP)' Intervention for Enhancing Therapeutic Exercise Adherence Among Patients With Greater Trochanteric Pain Syndrome (GTPS): A Feasibility Trial","ASAP","Inclusion Criteria:\n\n1. Diagnosis of Greater Trochanteric Pain Syndrome (GTPS): Participants must have been diagnosed with GTPS by a qualified healthcare provider\n2. Age: Participants aged 18 years or above\n3. Willingness to Participate: Participants must express a willingness to participate in the study\n4. Ability to Understand and Provide Informed Consent: Participants must be able to comprehend the study details, provide informed consent, and actively engage in the intervention and assessment processes\n5. Ability to Perform Prescribed Exercises: Participants should be physically able to perform the prescribed exercises safely to actively engage in the intervention as assessed by their NHS treating healthcare practitioner\n6. Having a mobile phone\n\nExclusion Criteria:\n\n1. Age: Participants aged under 18 years.\n2. Severe Medical or Psychiatric Conditions: Participants who suffer from severe medical or psychiatric disorders that could significantly impact their ability to engage in the intervention or comply with the exercise program will not be included.","ALL","18 Years",{"count":20,"type":21},60,"ESTIMATED","INTERVENTIONAL",[24],"NA","Greater Trochanteric Pain Syndrome (GTPS) is a condition that causes pain on the outer side of the hip. This clinical trial tests a simple exercise timing approach for adults with GTPS.\n\nThe main questions it aims to answer are:\n\n* Can enough people with GTPS be recruited and complete this study?\n* How many participants fill in their questionnaires at all five check-ins?\n* Do participants find the exercise timing approach easy and acceptable?\n\nResearchers will compare three groups. Each group receives different guidance on when to do their exercises. This will show whether timing guidance (with or without reminders) works better than usual care.\n\nParticipants will:\n\n* Follow a prescribed hip exercise programme set by their healthcare provider\n* Fill in a short daily survey (1-2 minutes) for 28 days\n* Complete online questionnaires about hip pain, movement, and exercise at five - points over about three months\n* Join an online group discussion at the end of the study\n\nAdults aged 18 and over may take part if they:\n\n* Have been diagnosed with GTPS by a healthcare provider\n* Are able to exercise safely\n* Own a mobile phone\n\nTaking part may help participants keep up with their prescribed exercises, which may in turn reduce hip pain and improve daily activities. It could also help researchers find better ways to support people with GTPS in the future.",[27,28],"Greater Trochanter Pain Syndrome","Hip Pain",[30,31,32,33,34,35,36],"Greater Trochanteric Pain Syndrome","Exercise adherence","Feasibility trial","Behavioural intervention","Hip pain","Rehabilitation","Exercise timing","RECRUITING","2026-05-15",{"date":40,"type":41},"2026-05-19","ACTUAL",{"date":43,"type":41},"2025-09-01",{"date":45,"type":21},"2027-03-31",{"name":47,"class":48},"Loughborough University","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":60,"briefSummary":61,"conditions":62,"keywords":65,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":49},"100640994","hips-feasibility-randomized-controlled-trial-100640994","NCT07586397","HIPS Feasibility Randomized Controlled Trial","HIPS Feasibility RCT Testing a Mind-Body Intervention to Improve Recovery for Individuals With Chronic Hip Pain","HIPS-RCT","Inclusion Criteria:\n\n1. Presenting with chronic (lasting ≥3 months) hip joint-related pain\n2. Fluent in English\n3. Age ≥18yr \\[If ≥45yr, the physician will confirm no osteoarthritis via X-ray (Kellgren Lawrence \\[KL\\] grade 0-1)\\]\n4. Score ≥3 for current hip pain on the Pain-VAS\n5. Psychological risk factor for the maintenance of pain by meeting ≥1 of the criteria listed below:\n\n   1. Score ≥ 20 on the PCS\n   2. Score ≤ 40 on the PSEQ\n   3. Score ≥ 17 on the TSK-11\n6. Exhibits sedentariness or dissatisfaction with physical activity by meeting ≥1 of the criteria listed below:\n\n   1. Physically active \\\u003C 150mins\u002Fweek according to the IPAQ-SF\n   2. Hip pain interferes with the ability to be physically active\n   3. Dissatisfaction with the current physical activity level\n\nExclusion Criteria:\n\n1. Previous surgery on the symptomatic (painful) hip\n2. Current pain referred from the lower back",{"count":59,"type":21},50,[24],"The goal of this clinical trial is to conduct a randomized controlled trial (RCT) to test the feasibility of two dose- and time-matched pain management programs, delivered via live video, for adults with chronic (lasting at least 3 months) and non-arthritic hip-related pain (HRP). Following pre-determined benchmarks, findings from this trial will be used to assess the feasibility, credibility, and acceptability of both programs (HIPS-1, HIPS-2). In preparation for a future clinical trial powered to test efficacy, we will optimize the protocol for patient recruitment, study protocol, and fidelity materials.",[63,28,64],"Hip Pain Chronic","Physical Medicine and Rehabilitation",[66,67,68],"Intervention feasibility","Randomized controlled trial","Behavioral intervention development","NOT_YET_RECRUITING","2026-05-13",{"date":38,"type":41},{"date":73,"type":21},"2026-06-01",{"date":75,"type":21},"2028-06-01",{"name":77,"class":48},"Massachusetts General Hospital",{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":85,"enrollmentInfo":86,"targetDuration":4,"studyType":22,"phases":88,"briefSummary":89,"conditions":90,"keywords":94,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":105,"lastUpdatePostDateStruct":106,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":49},"100635080","ultrasound-guided-needle-percutaneous-electrolysis-with-therapeutic-exercise-in-femoroacetabular-impingement-syndrome-100635080","NCT07548034","Ultrasound-guided Needle Percutaneous Electrolysis With Therapeutic Exercise in Femoroacetabular Impingement Syndrome","Effectiveness of Ultrasound-guided Percutaneous Needle Electrolysis Combined With Therapeutic Exercise in Femoroacetabular Impingement Syndrome: a Randomized Pilot Clinical Trial.","Inclusion Criteria:\n\n* Anterior hip pain (inguinal region) lasting more than 3 months\n* Numeric Rating Scale (NRS) pain score ≥ 4\u002F10 during at least one provocative test\n* Positive result in at least one of the following clinical tests: Straight Leg Raise (SLR), Flexion-Adduction-Internal Rotation (FADIR), or Hip-External Rotation-Flexion-Ceiling (HEC)\n* Ultrasound findings compatible with pseudofibrotic tissue near the iliopsoas tendon at the anterosuperior acetabular recess\n* Age between 18 and 55 years\n* Able to provide written informed consent\n\nExclusion Criteria:\n\n* Previous hip surgery\n* Moderate or severe hip osteoarthritis (diagnosed radiographically)\n* Neurological pathology affecting the lower limb\n* Dominant lumbar spine pathology\n* Active rheumatic or systemic inflammatory diseases\n* Any contraindication to percutaneous electrolysis\n* Belonephobia","55 Years",{"count":87,"type":21},30,[24],"Hip pain in the front of the hip is common and can make daily activities and sports difficult. One frequent cause is femoroacetabular impingement, also known as hip impingement.\n\nThis clinical trial is studying whether adding ultrasound-guided percutaneous electrolysis - a minimally invasive physiotherapy technique that uses a fine needle and a small electrical current - to a program of specific exercises works better than doing the exercises alone.\n\nParticipants will be randomly assigned to one of two groups:\n\n* One group will receive two sessions of percutaneous electrolysis plus a home exercise program.\n* The other group will follow the same home exercise program without percutaneous electrolysis.\n\nThe study will last five weeks. Researchers will measure pain, hip movement, and hip function at the beginning, after one week, and after four weeks. They will also record any side effects.\n\nThe main goal is to find out if adding percutaneous electrolysis helps reduce hip pain and improve function more than exercise alone. This pilot study will help determine if this technique could be a safe and effective non-surgical treatment option for people with pain in the front of the hip.",[91,28,92,93],"Femoro Acetabular Impingement","Iliopsoas Syndrome","Groin Pain",[95,96,97,98,99,100,101,102,103,104],"Percutaneous needle electrolysis","Therapeutic exercise","Anterior hip pain","Iliopsoas","Hip function","Range of motion","Pain intensity","Ultrasound-guided therapy","Conservative treatment","Ultrasound-Guided Percutaneous Needle Electrolysis","2026-04-29",{"date":107,"type":41},"2026-05-05",{"date":109,"type":41},"2026-04-22",{"date":111,"type":21},"2027-07-01",{"name":113,"class":48},"CEU San Pablo University",{"id":115,"slug":116,"hasResults":11,"nctId":117,"briefTitle":118,"officialTitle":119,"acronym":4,"eligibilityCriteria":120,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":121,"enrollmentInfo":122,"targetDuration":4,"studyType":22,"phases":124,"briefSummary":125,"conditions":126,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":49},"100417833","categorized-pt-for-non-arthritic-hip-and-groin-pain-100417833","NCT04720846","Categorized PT for Non-arthritic Hip and Groin Pain","Assessment of a Categorized Physical Therapy Protocol for Non-arthritic Hip and Groin Pain: a Randomized Controlled Study","Inclusion Criteria:\n\n* New patient presenting with non-arthritic hip impingement, hip pain, and groin pain (Tonnis 0-1)\n* 18-60 years old\n\nExclusion Criteria:\n\n* Arthritic hip pain (Tonnis 2+)\n* \\\u003C18 and \\>60 years old\n* History of spinal fusion surgery\n* History of low back pain with radicular pain\n* History of hip arthroscopy\n* History of inflammatory conditions, and other concurrent problems interfering with hip therapy (i.e., concurrent back\u002Fknee\u002Ffoot\u002Fankle\u002Fshoulder issues)\n* Patients currently taking TNF-alpha inhibitors for inflammatory conditions\n* History of prior knee osteotomy\n* Non-English speakers","60 Years",{"count":123,"type":21},70,[24],"There is currently limited literature on a categorized physical therapy protocol for management of hip pain. Only a handful of studies have looked at the treatment of osteoarthritis of the hip with a standardized physical therapy treatment, primarily looking at manual therapy versus exercise therapy protocols. However, there are no studies observing the effect of a standardized physical therapy program on patients presenting with non-arthritic hip and groin pain. Based on the gap in the literature, this study will aim to assess the effect of matrix-based standard of care therapy in patients presenting with non-arthritic hip and groin pain.",[28,93],"2026-04-23",{"date":129,"type":41},"2026-04-28",{"date":131,"type":41},"2020-12-02",{"date":133,"type":21},"2027-02",{"name":135,"class":48},"Hospital for Special Surgery, New York",{"id":137,"slug":138,"hasResults":11,"nctId":139,"briefTitle":140,"officialTitle":141,"acronym":4,"eligibilityCriteria":142,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":143,"enrollmentInfo":144,"targetDuration":4,"studyType":22,"phases":145,"briefSummary":146,"conditions":147,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":155,"lastUpdatePostDateStruct":156,"startDateStruct":158,"completionDateStruct":160,"leadSponsor":162,"locationsCount":49},"100594265","opposed-anterior-hip-arthroplasty-regional-anesthesia-study-study-100594265","NCT07017192","OPPOSED (anteriOr hiP arthroPlasty regiOnal aneSthEsia stuDy) Study","OPPOSED (anteriOr hiP arthroPlasty regiOnal aneSthEsia stuDy) Study. Regional Anesthesia Techniques for Anterior Approach Hip Arthroplasty Analgesia: SIFI Block Versus Lumbar ESP Block","Inclusion Criteria:\n\n* Age \\>=18 years and =\\\u003C85 years\n* patients undergoing elective unilateral THA with direct anterior approach\n* patients able to understand the purposes of the study and provide signed informed consent\n\nExclusion Criteria:\n\n* pregnancy\n* Age \\\u003C18 years or \\>85 years\n* revision or bilateral surgeries\n* psychiatric pathology or cognitive deficits, mental retardation, inability to provide valid informed consent\n* History of illicit drugs and\u002For alcohol abuse\n* urgent\u002Femergent surgery with admission to Intensive Care under sedation and mechanical ventilation or complications that do not allow evaluation\n* known allergy to the drugs used in the study\n* refusal to provide informed consent","85 Years",{"count":59,"type":21},[24],"Main indications for total hip arthroplasty (THA) are degenerative osteoarthritis of the coxofemoral joint, osteonecrosis of the hip, congenital disorders such as dysplasia and inflammatory arthritis. More recently, surgery using the direct anterior approach is getting popularity: this method, in fact, granting a significant sparing of the hip muscles, is associated with favorable results compared to other techniques, such as a lower risk of dislocation, limitated damage to soft tissues with better recovery and early discharge.\n\nPatients undergoing this procedure may although experience moderate to severe postoperative pain in the first few hours (with peaks observed in the first 12 hours), as well as potential complications such as nausea and vomiting related to opioids use.\n\nIt has been shown that adequate pain control influences early mobilization and rehabilitation, ensuring a quicker recovery. The role of regional anesthesia techniques has been established in almost all areas of orthopedic surgery, and in particularly in the management of postoperative pain following hip replacement surgery, but definitive data are missing with regard to direct anterior approach.\n\nRegional anesthesia consists of infiltrating local anesthetics in sites (fascial planes or nerves), in order to limit or even eliminate the use of traditional painkillers, with a significant reduction in the side effects.\n\nThe aim of this study is to compare the impact of two techniques, the Suprainguinal Fascia Iliaca (SIFI) block and the lumbar Erector Spinae Plane (ESP) block, in managing postoperative pain in subjects undergoing total hip replacement surgery performed by direct anterior approach.\n\nThe primary objective of the study is the incidence of residual femoral and obturator nerves block (knee extension and hip adduction according to ASIA score) 8 hours after surgery in the two treatment groups.\n\nSecondary objectives include: • Time elapsed between the end of surgery and the recovery of lower limb motility enough to allow the patient to mobilize independently; • Total opioid consumption (calculated as morphine equivalents) at 8, 24 and 48 hours after surgery; • Pain according to NRS (numerica rating scale) at 8, 24 and 48 hours after surgery; • Extent of sensory block of the three branches of the lumbar plexus (femoral, obturator, lateral femorocutaneuous nerves) at 8, 24 and 48 hours after surgery; • Timing of hospital discharge; • Incidence of chronic or persistent postoperative pain (at 30 and 90 days after surgery); • Any postoperative complication",[148,149,28,150,151,152,153,154],"Hip Replacement Surgery","Hip Replacement, Total","Hip Arthroplasty","Hip Replacement Postoperative","Hip Surgery","Pain,Postoperative","Mobility and Independence","2025-06-27",{"date":157,"type":41},"2025-06-29",{"date":159,"type":41},"2025-06-23",{"date":161,"type":21},"2026-09-23",{"name":163,"class":48},"A.O.U. Città della Salute e della Scienza"]