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Endometriosis and Risk of Miscarriage

NCT ID: NCT03354780

Last Updated: 2017-11-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

844 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-01-15

Study Completion Date

2017-10-04

Brief Summary

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The aim of this study is to compare the rate of miscarriage at first spontaneous pregnancy among women with endometriosis with the rate of miscarriage at first spontaneous pregnancy among women without endometriosis.

Detailed Description

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All women followed up for a surgical or sonographic diagnosis of endometriosis in 11 italian referral Centres for the treatment of endometriosis completed a questionnaire regarding their previous pregnancies. The same questionnaire was completed by women, attending a routine gynecologic visit, in whom surgery or vaginal examination and pelvic ultrasonography excluded endometriosis.

Conditions

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Endometriosis Miscarriage

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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endometriosis

Survey on first pregnancy after endometriosis diagnosis

Survey on first pregnancy after endometriosis diagnosis

Intervention Type OTHER

rate of miscarriage was noted

non endometriosis

Survey on first pregnancy

Survey on first pregnancy

Intervention Type OTHER

rate of miscarriage was noted

Interventions

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Survey on first pregnancy after endometriosis diagnosis

rate of miscarriage was noted

Intervention Type OTHER

Survey on first pregnancy

rate of miscarriage was noted

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 30 to 50 years old women
* with at least one previous spontaneous pregnancy
* with surgical or clinical/sonographic diagnosis of endometriosis or
* in whom surgical or clinical/sonographic evaluation ruled out endometriosis

Exclusion Criteria

* Pregnancy achieved by Assisted Reproductive technology
* Biochemical pregnancy
* Non corrected uterine malformation, poliabortivity, lupus like anticoagulant
Minimum Eligible Age

30 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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University of Milan

OTHER

Sponsor Role collaborator

Endometriosis Treatment Italian Club

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Nicola Berlanda, MD

Role: PRINCIPAL_INVESTIGATOR

Endometriosis Treatment Italian Club

Other Identifiers

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ETIC001

Identifier Type: -

Identifier Source: org_study_id