[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT06268951":3,"trial-entities:NCT06268951":64,"trial-summary:NCT06268951":68},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":6,"overall_status":7,"completion_date":8,"status_verified_date":9,"last_update_date":10,"start_date":11,"sponsor_name":12,"lead_sponsor_class":13,"has_dmc":14,"brief_summary":15,"detailed_description":16,"conditions":17,"keywords":19,"study_type":21,"primary_purpose":22,"phases":23,"enrollment_info":24,"interventions":27,"primary_outcomes":28,"secondary_outcomes":33,"sex":34,"minimum_age":22,"maximum_age":22,"healthy_volunteers":14,"eligibility_criteria":35,"std_ages":41,"locations":45,"central_contacts":54,"overall_officials":55,"references":59,"see_also_links":60},"NCT06268951","23-005485","Recovery and Symptom Relief Following Percutaneous Ablation of Abdominal Wall Endometriosis","ENROLLING_BY_INVITATION","2028-12","2026-05","2026-06-02","2024-05-09","Mayo Clinic","OTHER",false,"To determine the characteristics of recovery and symptom relief following ablation of abdominal wall endometriosis.","The purpose of this study is to characterize the recovery and symptom relief following cryoablation of abdominal wall endometriosis. Patients undergoing clinically indicated ablation of abdominal wall endometriosis will receive an endometriosis-specific symptom survey (Endometriosis Health Profile - 30) prior to ablation and then at 3-, 6-, 12-, and 24-months following treatment. A 2 question survey related to pain at the treatment site will also be administered prior to ablation and then at 1-, 7-, and 30-days after ablation.",[18],"Endometriosis",[20],"Abdominal Wall endometriosis","OBSERVATIONAL",null,[],{"count":25,"type":26},50,"ESTIMATED",[],[29],{"measure":30,"description":31,"timeFrame":32},"Symptom severity due to abdominal wall endometriosis following ablation.","Using the Endometriosis Health Profile - 30 survey, the impact of ablation on endometriosis-related symptoms will be quantified over time. A numerical rating scale will be used to quantify pain at the site of treated abdominal wall endometriosis.","Baseline and intermittently over 24 months",[],"FEMALE",{"inclusion":36,"exclusion":38,"raw_text":40},[37],"Undergoing ablation for abdominal wall endometriosis.",[39],"Decline to participate in research.","Inclusion Criteria:\n\n* Undergoing ablation for abdominal wall endometriosis.\n\nExclusion Criteria:\n\n* Decline to participate in research.",[42,43,44],"CHILD","ADULT","OLDER_ADULT",[46],{"facility":12,"city":47,"state":48,"zip":49,"country":50,"geoPoint":51},"Rochester","Minnesota","55905","United States",{"lat":52,"lon":53},44.02163,-92.4699,[],[56],{"name":57,"affiliation":12,"role":58},"Thomas Atwell, M.D.","PRINCIPAL_INVESTIGATOR",[],[61],{"label":62,"url":63},"Mayo Clinic Clinical Trials","https:\u002F\u002Fwww.mayo.edu\u002Fresearch\u002Fclinical-trials",{"nct_id":4,"conditions":65,"biomarkers":67},[66],"Abdominal Wall Endometriosis",[],{"nct_id":4,"found":14,"summary":22,"prompt_version":22}]