[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"achilles-tendon-injury\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:achilles-tendon-injury":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,77],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":31,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100642048","morphological-and-mechanical-assessment-in-the-achilles-tendon-after-radiofrequency-stimulation-in-runners-100642048",false,"NCT07648199","Morphological and Mechanical Assessment in the Achilles Tendon After Radiofrequency Stimulation in Runners","Morphological and Mechanical Changes in the Achilles Tendon After the Application of INDIBA® Therapy in Healthy Runners: A Pre-post Quasi-experimental Study","RFAchillesRun","Inclusion Criteria:\n\n* Adults aged 18-65\n* Runners with at least one year of regular practice.\n* Must not have suffered any ligament, bone, tendon, or muscle injury in the lower limb or lumbar region during the last year.\n\nExclusion Criteria:\n\n* History of lower limb surgery, rheumatic or neuromuscular diseases or pregnancy\n* Contraindication for radiofrecuency treatment.\n* Athletes with visual, auditory, or any other impairment that may affect their cognitive ability to understand the test.",true,"ALL","18 Years","65 Years",{"count":22,"type":23},19,"ESTIMATED","INTERVENTIONAL",[26],"NA","448 kHz capacitive-resistive monopolar radiofrequency is an emerging physiotherapy technique whose usefulness and clinical relevance still need to be investigated. This study is a pre-post quasi-experimental study in which several variables will be measured before and immediately after 448 kHz capacitive resistive monopolar radiofrequency. It aims to analyze the morphological and mechanical changes in the Achilles tendon following the intervention in healthy runners.",[29,30],"Achilles Tendon Injury","Achilles Tendon",[32,33,34],"Achilles tendon","Radiofrecuency","Physiotherapy","NOT_YET_RECRUITING","2026-06-14",{"date":38,"type":39},"2026-06-17","ACTUAL",{"date":41,"type":23},"2026-07-01",{"date":43,"type":23},"2026-07-30",{"name":45,"class":46},"University of Malaga","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":24,"phases":57,"briefSummary":59,"conditions":60,"keywords":63,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":76},"100576047","phase-2-assessment-of-medrol-dosepak-to-reduce-opioid-consumption-in-foot-and-ankle-surgical-patients-100576047","NCT06780202","Assessment of Medrol Dosepak to Reduce Opioid Consumption in Foot and Ankle Surgical Patients","Inclusion Criteria:\n\n-Emory Orthopedic patients undergoing foot and ankle surgery\n\nExclusion Criteria:\n\n* Concurrent or significant injuries to other bones or organs\n* Local infections\n* History of alcohol or medical abuse, including prior opioid abuse\n* Smoking\n* History of severe heart disease, renal failure, liver dysfunction, active peptic ulcer disease, diabetes, rheumatoid arthritis, neurological or psychiatric diseases that could influence pain perception\n* Pre-existing immune suppression\n* Those deemed possibly non-compliant by the study team and,\n* All vulnerable populations (those unable to give consent, juveniles, pregnant women, prisoners, cognitively impaired and non-English speaking).","95 Years",{"count":56,"type":23},180,[58],"PHASE2","This clinical trial aims to determine the effects of a 6-day low-dose methylprednisolone course on pain, nausea, and total opioid consumption in patients undergoing foot and ankle surgeries.\n\nThe secondary objective of the study is to determine and monitor the effects of the course on complications following surgery and patient-reported outcomes",[61,62,29],"Foot Injuries and Disorders","Ankle Injuries and Disorders",[64,65],"VAS scale: visual analog scale","Medrol Dosepak","RECRUITING","2026-03-05",{"date":69,"type":39},"2026-03-09",{"date":71,"type":39},"2025-01-27",{"date":73,"type":23},"2027-12",{"name":75,"class":46},"Emory University",2,{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":81,"acronym":82,"eligibilityCriteria":83,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":84,"targetDuration":86,"studyType":87,"phases":4,"briefSummary":88,"conditions":89,"keywords":91,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":4},"100618345","cuhk-achilles-tendon-disorder-registry-100618345","NCT07330414","CUHK Achilles Tendon Disorder Registry","AT Registry","Inclusion Criteria:\n\n* Adults (\\>18 years of age)\n\nExclusion Criteria:\n\n* Any physical or psychological comorbidity that would impair the ability to complete study assessments (e.g., significant neurological deficits) or preclude the provision of informed consent.\n* Concomitant diseases that severely affect lower limb function or assessment (e.g., severe osteoarthritis of the knee or hip, prior lower limb amputation, peripheral vascular disease, active rheumatoid arthritis, lower limb paralysis, etc.)",{"count":85,"type":23},200,"5 Years","OBSERVATIONAL","This is a long-term research registry for patients with Achilles tendon disorders (like tears, chronic pain, or ruptures) as well as healthy adults without tendon problems. The goal is to collect detailed information over time to understand which treatments work best for different people, identify risk factors for injury, and improve overall care. Adults over 18, both with and without Achilles tendon conditions, are eligible to join. Participants will attend several assessment visits at the Prince of Wales Hospital over the first year (at the start, 6 weeks, 3, 4, 6, and 12 months) for physical tests, ultrasounds, and questionnaires. After the first year, follow-up continues with annual online questionnaires for up to five years. The main measure is a standard questionnaire about tendon pain and function (VISA-A). The study aims to use this information to guide better, more personalized rehabilitation strategies, improve patient outcomes, and reduce long-term disability. All participation is voluntary and requires written consent.",[29,30,90],"Achilles Tendon Pain",[92,93,94],"Achilles tendinopathy","Achilles tendon rupture","Achilles tendinitis","2025-12-28",{"date":97,"type":39},"2026-01-09",{"date":99,"type":23},"2026-01-15",{"date":101,"type":23},"2030-12-30",{"name":103,"class":46},"Chinese University of Hong Kong"]