Recovery and Symptom Relief Following Percutaneous Ablation of Abdominal Wall Endometriosis

NCT06268951 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2025-05-31

No results posted yet for this study

Summary

To determine the characteristics of recovery and symptom relief following ablation of abdominal wall endometriosis.

Conditions

  • Endometriosis

Sponsors & Collaborators

Principal Investigators

  • Thomas Atwell, M.D. · Mayo Clinic

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-05-09
Primary Completion
2027-02-28
Completion
2027-12-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06268951 on ClinicalTrials.gov