Patient-reported Outcomes Following Percutaneous Ablation of Desmoid Tumors

This study will evaluate patient-reported outcomes before and after percutaneous ablation of desmoid tumors. Adult participants undergoing ablation for desmoid tumor will complete surveys pre and post procedure to assess symptom burden, impact on daily life, early post-procedural pain and recovery, concomitant treatments, and radiological response following ablation.

NCT Number	NCT07755176
Lead Sponsor	Mayo Clinic
Conditions	Desmoid Tumor, Aggressive Fibromatoses
Enrollment	30 participants
Start Date	2026-09-01
Primary Completion	2028-12-31 (estimated)
Study Completion	2028-12-31 (estimated)
Updated on ClinicalTrials.gov	2026-08-10