Recovery and Symptom Relief Following Percutaneous Ablation of Abdominal Wall Endometriosis

Part of paid clinical trials in Rochester, Minnesota.

Sponsor
Mayo Clinic
Study ID
NCT06268951
Status
Enrolling By Invitation

Conditions

Eligibility Criteria

Sex
FEMALE
Age
N/A - N/A
Healthy Volunteers
Not accepted

Study Details

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

Key Dates

Start date
May 9, 2024
Status verified
May 2026
Primary completion
Feb 29, 2028
Completion
Dec 31, 2028

Study Design

Enrollment
50 participants (estimated)

Primary Outcome Measure

Symptom severity due to abdominal wall endometriosis following ablation. [ Time Frame: Baseline and intermittently over 24 months ]

Locations (1)

FacilityCityStateZIPSite coordinators
Mayo ClinicRochesterMinnesota55905-

Find similar trials in Rochester, MN

By condition
Endometriosis
By specialty
Women's healthFertility
By research site
Mayo Clinic· Rochester, MN

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