MedTrace Logo

The North-West Inter Regional Female Cohort for Patients With Endometriosis

NCT02294825 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1500

Last updated 2019-10-24

No results posted yet for this study

Summary

All women managed for endometriosis are included and followed up through the CIRENDO database.

Information is obtained from surgical and histological records and from self-questionnaires completed before surgery. Standardized gastrointestinal questionnaires (KESS, GIQLI, WEXNER, FIQL and Bristol) are routinely used to assess bowel function. Data recording, patient contact and follow-up are carried out by a clinical research technician. Postoperative follow-up is based on data from the afore-mentioned questionnaires completed at 1, 3, 5 and 7 years.

Conditions

  • Endometriosis

Interventions

PROCEDURE

various surgical procedures in endometriosis

Shaving, disc excision and colorectal resection; ureterolysis or ureter resection; bladder resection; ablation of endometriomas using plasma energy; excision and ablation of deep and superficial lesions

Sponsors & Collaborators

  • University Hospital, Lille

    collaborator OTHER

  • University Hospital, Caen

    collaborator OTHER

  • Amiens University Hospital

    collaborator OTHER

  • University Hospital, Rouen

    lead OTHER

Principal Investigators

  • Horace Roman · University Hospital, Rouen

Eligibility

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

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2022-06-30
Completion
2022-06-30

Countries

  • France

Study Locations

More Related Trials

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 NCT02294825 on ClinicalTrials.gov