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A Study on the Prognosis of Two Different Surgery Methods in Patients With Rectal Endometriosis

NCT06254716 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 90

Last updated 2024-02-12

No results posted yet for this study

Summary

This retrospective study aims to compare the surgical and pregnancy outcomes of disc and segmental resection for rectal DIE through a single-center retrospective analysis, to summarize clinical experience, and to explore the possible factor of the differences. The results would provide preliminary clinical basis for the treatment and selection of surgical methods for patients with rectal DIE, and also provide a research basis for the prospective clinical studies.

Conditions

  • Gastrointestinal Function
  • Quality of Life
  • Pregnancy Outcomes

Interventions

PROCEDURE

disc resection

disc resection refers to the full-thickness resection of the lesion and the intestinal wall, usually anterior rectal wall. During the operation, the anterior intestinal wall is opened and then sutured or anastomosed with a stapler. Segmental bowel resection for the treatment of intestinal endometriosis was first reported by Redwine and Sharpe in 1991, which requires the maximum removal of endometriosis lesions.

PROCEDURE

segmental resection

Segmental bowel resection for the treatment of intestinal endometriosis was first reported by Redwine and Sharpe in 1991, which requires the maximum removal of endometriosis lesions.

Sponsors & Collaborators

  • Fudan University

    lead OTHER

Principal Investigators

  • Wei Zhang, Ph.D. · OB & GYN Hospital of Fudan University

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-01
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • China

Study Locations

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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 NCT06254716 on ClinicalTrials.gov