Skip to main content
Clinical Trials/NCT01833013
NCT01833013
Unknown
Not Applicable

Infertility and Endometriosis : a Prospective Cohort Study

University Hospital, Montpellier1 site in 1 country200 target enrollmentApril 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endometriosis
Sponsor
University Hospital, Montpellier
Enrollment
200
Locations
1
Primary Endpoint
live birth date
Last Updated
11 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
April 2013
End Date
October 2018
Last Updated
11 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

live birth date

Time Frame: 3 years

Assessment of the number of live birth in the 3 years following the laparoscopic exploration making the diagnosis of endometriosis

Secondary Outcomes

  • Quality of life(3 years)
  • pain symptoms(3 years)

Study Sites (1)

Loading locations...

Similar Trials