Actively Recruiting
Impact of Complete Surgery of Colorectal Deep Infiltrating Endometriosis on Fertility
Led by University Hospital, Lille · Updated on 2026-04-22
120
Participants Needed
5
Research Sites
493 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Lille
Lead Sponsor
M
Ministry of Health, France
Collaborating Sponsor
AI-Summary
What this Trial Is About
The ENDOFERT Study is an open, multicenter, randomized, parallel-group, controlled trial. This study includes patients presenting colorectal DIE and infertility. Patients will be randomized in two parallel-groups; one group underwent complete surgery of colorectal DIE prior to ART and the other group underwent ART alone (ratio 1:1)
CONDITIONS
Official Title
Impact of Complete Surgery of Colorectal Deep Infiltrating Endometriosis on Fertility
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Primary or secondary infertility
- Indication for IVF treatment
- Persistent pain related to endometriosis despite medical pain treatment
- Persistent pain including at least one digestive symptom related to endometriosis: dyschesia, sub-occlusive syndrome, rectal bleeding, or painful defecation
- Colorectal deep infiltrating endometriosis confirmed by MRI and at least one additional imaging method
- Eligible for deep infiltrating endometriosis surgery
You will not qualify if you...
- Contraindication to pregnancy or IVF
- Viral risk
- Previous IVF cycles
- Previous colorectal surgery
- Need for myomectomy during surgery
- Use of donor oocytes
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 5 locations
1
CHU
Clermont-Ferrand, France
Actively Recruiting
2
Hôpital Jeanne de Flandres, CHRU
Lille, France
Actively Recruiting
3
AP-HP, Hôpital Tenon
Paris, France
Actively Recruiting
4
CHU
Poissy, France
Actively Recruiting
5
CHU
Rouen, France
Actively Recruiting
Research Team
P
Pierre Collinet, MD,PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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