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NCT06268951 Clinical Trial

Recovery and Symptom Relief Following Percutaneous Ablation of Abdominal Wall Endometriosis

Endometriosis Clinical Trial

Official title:
Recovery and Symptom Relief Following Percutaneous Ablation of Abdominal Wall Endometriosis

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT06268951
Other study ID # 23-005485
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date May 9, 2024
Est. completion date December 2027

Study information
Verified date May 2024
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Description:

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.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 50
Est. completion date December 2027
Est. primary completion date February 2027
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - Undergoing ablation for abdominal wall endometriosis. Exclusion Criteria: - Decline to participate in research.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Mayo Clinic Rochester Minnesota

Sponsors (1)
Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary 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
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