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Infertility and Endometriosis Cohort

Infertility and Endometriosis : a Prospective Cohort Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01833013
Acronym
EndoFertil
Enrollment
200
Registered
2013-04-16
Start date
2013-04-30
Completion date
2018-10-31
Last updated
2015-01-09

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

Conditions

Endometriosis, Infertility

Keywords

Endometriosis, Cohort study, fertility, pregnancy, assisted reproductive technics, laparoscopy

Brief summary

Nowadays, one in six couples consults for fertility problems. If the standard examination and tests do not reveal any cause of infertility, the woman may undergo a laparoscopic exploration which reveals endometriosis in more than 50% of cases. Endometriosis is an inflammatory disease defined as the presence of endometrial tissue out of the uterine cavity. It is frequent (1 in 10 women) and associated with a high economic burden (22 billion dollars in 2002 in the USA) and important decrease in quality of life. Physiopathological mechanisms and risk factors for endometriosis are not well identified. A woman with endometriosis is 20 times more at risk of infertility. Fecundity rate of a 25-year-old couple is about 15 to 20% in the general population and only 2 to 10% in case of endometriosis. There are many manifestations of this disease (infertility, pelvic pain) and the anatomo-clinical correlation is not good. The presently used international classification (American Fertility Society revised in 1985, AFSr) does not predict the chance of pregnancy. New scores such as the Endometriosis Fertility Index (EFI) have been proposed to do so, but need to be validated. Treatment for endometriosis-related infertility is not consensual. A prospective cohort study would give access to clinical data of patients followed in our center, so as to identify clinical factors predicting pregnancy and to help treatment decision for women with endometriosis suffering from infertility.

Interventions

OTHERlive birth date and quality of life assessment

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 41 Years
Healthy volunteers
No

Inclusion criteria

* Woman from 18 to 41 years old. * Dealing with infertility, * With a normal pelvic echography and hysterosalpingography, a normal hormonal status and a partner with a normal sperm. * For whom a laparoscopic exploration finds endometriosis. * Consenting to participate to the study.

Exclusion criteria

* Any contraindication for general anesthesia or for laparoscopy. * Any contraindication for pregnancy. * Follow-up is impossible. * Consent is impossible.

Design outcomes

Primary

MeasureTime frameDescription
live birth date3 yearsAssessment of the number of live birth in the 3 years following the laparoscopic exploration making the diagnosis of endometriosis

Secondary

MeasureTime frameDescription
Quality of life3 yearsAssessment of the quality of life relating to infertility and endometriosis in the 3 years following laparoscopic exploration making the diagnosis of endometriosis.
pain symptoms3 yearsAssessment of the pain symptoms relating to infertility and endometriosis in the 3 years following laparoscopic exploration making the diagnosis of endometriosis.

Countries

France

Contacts

Primary ContactHerve Dechaud, MD,PhD
h-dechaud@chu-montpellier.fr+33467336532
Backup Contactclaire chauveton, pharmD
c-chauveton@chu-montpellier.fr+33467330924

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026