[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"chronic-heel-pain\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:chronic-heel-pain":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"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":30,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":5},"100646777","pulsed-radiofrequency-versus-5-dextrose-injection-in-chronic-plantar-fasciitis-100646777",false,"NCT07688876","Pulsed Radiofrequency Versus 5% Dextrose Injection in Chronic Plantar Fasciitis","Comparison of Ultrasound-Guided Pulsed Radiofrequency and 5% Dextrose Injection in Patients With Chronic Plantar Fasciitis: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Diagnosis of chronic plantar fasciitis based on medical history and physical examination\n* Heel pain resistant to conservative treatment for at least 12 weeks\n* Age between 18 and 70 years\n* Willingness to participate in the study and provide written informed consent\n\nExclusion Criteria:\n\n* Congenital or acquired disease that may impair or prevent foot function, such as rheumatoid arthritis, hemiplegia, congenital foot deformity, traumatic foot or leg amputation, or fracture sequelae\n* Local infection or skin disease at the treatment site\n* Bleeding disorder or use of anticoagulant medication within the last week\n* Disease causing mental dysfunction, such as uncontrolled Parkinson disease or Alzheimer disease\n* Previous surgery for plantar fasciitis\n* Refusal to participate in the study or inability to provide informed consent\n* Failure to attend follow-up visits after treatment\n* Request to withdraw from the study\n* Pregnancy or suspected pregnancy\n* Presence of a cardiac pacemaker\n* History of epilepsy\n* Active or previous malignancy\n* Rheumatologic disease","ALL","18 Years","70 Years",{"count":20,"type":21},50,"ESTIMATED","INTERVENTIONAL",[24],"NA","This prospective, two-center, randomized controlled clinical trial aims to compare the effectiveness of ultrasound-guided pulsed radiofrequency and 5% dextrose injection in patients with chronic plantar fasciitis. Eligible participants will be randomized into two parallel groups. One group will receive ultrasound-guided pulsed radiofrequency treatment, and the other group will receive ultrasound-guided 5% dextrose injection using the peppering technique. All participants will receive a home-based plantar fascia stretching exercise program. Outcomes will be assessed at baseline, 3 weeks, 6 weeks, and 12 weeks after treatment. The primary outcome will be pain intensity measured by the Numeric Rating Scale. Secondary outcomes will include foot function, activity-related pain, ankle-hindfoot function, and health-related quality of life.",[27,28,29],"Chronic Plantar Fasciitis","Chronic Heel Pain","Foot Pain",[31,32,33,34,35,36,37,38,39,40,41],"Pulsed radiofrequency","Radiofrequency treatment","Dextrose injection","Prolotherapy","Ultrasound-guided injection","Plantar fascia","Chronic heel pain","Numeric Rating Scale","Foot Function Index","AOFAS score","Nottingham Health Profile","RECRUITING","2026-06-30",{"date":45,"type":46},"2026-07-07","ACTUAL",{"date":48,"type":46},"2026-01-01",{"date":50,"type":21},"2027-01-01",{"name":52,"class":53},"Ankara City Hospital Bilkent","OTHER"]