Impact of Endometriosis on Pregnancy and Delivery - a Retrospective Cohort Study

NCT ID: NCT04664335

Last Updated: 2022-08-22

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

1762 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-12-01

Study Completion Date

2020-12-01

Brief Summary

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Purpose:

To study the impact of endometriosis on subsequent pregnancy and delivery.

Methods:

retrospective analysis by questionnaire / interview of cases (endometriosis laparoscopically removed / child wish) vs. controls (endometriosis laparoscopically excluded / child wish) from the University Hospital Muenster, Germany, treated between 2009 and 2016; analysis of pregnancy rate, mode of delivery and complications using Clavien-Dindo-classification, role of deep infiltrating endometriosis using ENZIAN classification; data analysis using t-test with p \< 0.050% being considered significant.

Detailed Description

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Conditions

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Endometriosis Pregnancy Complications Delivery Complication Complication Miscarriage

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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endometriosis cases

endometriosis laparoscopically removed / child wish

questionnaire

Intervention Type OTHER

if no Reply to questionnaire, telephone interview

controls

endometriosis laparoscopically excluded / child wish

questionnaire

Intervention Type OTHER

if no Reply to questionnaire, telephone interview

Interventions

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questionnaire

if no Reply to questionnaire, telephone interview

Intervention Type OTHER

Other Intervention Names

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interview

Eligibility Criteria

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Inclusion Criteria

* cases: Operation because of endometriosis at the endometriosis Center, University Hospital Muenster, child wish, wants to participate, correct age group
* controls: Operation because of sterility, exclusion of endometriosis during this Operation, child wish, wants to participate, correct age group

Exclusion Criteria

* cases / controls: declines participation, incorrect age Group, no child wish
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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University Hospital Muenster

OTHER

Sponsor Role lead

Responsible Party

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Dr. med. Sebastian Daniel Schäfer

Head of Gynecology

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Sebastian D Schaefer, MD PhD

Role: PRINCIPAL_INVESTIGATOR

University Hospital Muenster, Germany

Locations

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University Hospital Münster Germany

Münster, North Rhine-Westphalia, Germany

Site Status

Countries

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Germany

Other Identifiers

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Schäfer_Endo_Preg_Del_Comp

Identifier Type: -

Identifier Source: org_study_id

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