Recovery and Symptom Relief Following Percutaneous Ablation of Abdominal Wall Endometriosis
NCT ID: NCT06268951
Last Updated: 2025-05-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ENROLLING_BY_INVITATION
50 participants
OBSERVATIONAL
2024-05-09
2027-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
FEMALE
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Thomas D. Atwell
Principal Investigator
Principal Investigators
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Thomas Atwell, M.D.
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic
Rochester, Minnesota, United States
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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23-005485
Identifier Type: -
Identifier Source: org_study_id
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