Assessment of the bowel from women that underwent surgery for intestinal endometriosis

Recruiting

• Conditions: Endometriosis of intestine; M01.975

• Registration Number: RBR-7zrm8fd
• Lead Sponsor: Irmandade da Santa Casa de Misericórdia de São Paulo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-04-16
• Last Update Posted: 29 April 2024
• Study Completion: 2025-07-30

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Female patients; with clinical and radiological suspicion of deep endometriosis with intestinal involvement, who underwent imaging investigation using transvaginal ultrasound with intestinal preparation to map the endometriosis or Nuclear Magnetic Resonance Imaging with the same intestinal preparation technique; and had suspected intestinal involvement under 4 cms; with a degree of circumference in the intestinal involvement less than 40% and with a distance from the lesion less than 15 cms from the anal verge

Exclusion Criteria

Patients who do not present clinical and diagnostic characteristics in the evaluation that include them in the indications for the lumpectomy technique; the impossibility of completing the questionnaire within the allotted time (PRE, P3, P6 and P12); failure to complete the Informed Consent Form

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To assess intestinal function in women with intestinal endometriosis

Secondary Outcome Measures

Name	Time	Method
To assess intestinal function in women with intestinal endometriosis pre- and post-operatively