Skip to content

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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02294825
Acronym
CIRENDO
Enrollment
1500
Registered
2014-11-19
Start date
2009-06-30
Completion date
2022-06-30
Last updated
2019-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis

Keywords

deep endometriosis;, colorectal endometriosis, surgery, medical treatment, fertility

Brief 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.

Detailed description

All women managed for endometriosis are included and followed up through the CIRENDO database (the North-West Inter Regional Female Cohort for Patients with Endometriosis), a prospective cohort financed by the G4 Group (The University Hospitals of Rouen, Lille, Amiens and Caen), and coordinated by the principal investigator (H.R.). 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. Women are included in the CIRENDO database only when endometriosis is confirmed by both surgical exploration and biopsy. Postoperative follow-up is based on data from the afore-mentioned questionnaires completed at 1, 3, 5 and 7 years. Prospective data recording and analysis were approved by the French authorities CNIL (Commission Nationale de l'Informatique et des Libertés) and CCTIRS (Comité Consultatif pour le Traitement de l'Information en matière de Recherche dans le domaine de la Santé).

Interventions

PROCEDUREvarious 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

University Hospital, Lille
CollaboratorOTHER
University Hospital, Caen
CollaboratorOTHER
Amiens University Hospital
CollaboratorOTHER
University Hospital, Rouen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Endometriosis revealed on histological specimens

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Recurrences7 yearsrate of recurrences at 1,3,5 and 7 years postoperatively

Secondary

MeasureTime frameDescription
Risk factors for endometriosis1 yearAssociation of various antecedents with specific localizations of features of the endometriosis
Digestive functional outcomes7 yearsBowel function in patients managed for bowel endometriosis by various procedures
Fertility7 yearsRate of pregnancy at 1, 3, 5, and 7 years postoperatively

Countries

France

Contacts

Primary ContactHorace Roman
horace.roman@gmail.com+33 232 888 745

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 15, 2026