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Endometriosis and Obstetric Outcomes

A

Azienda Ospedaliero-Universitaria di Modena

Status

Unknown

Conditions

Endometriosis
Obstetric Complication

Treatments

Other: Retrospective analysis of obstetrics outcomes

Study type

Observational

Funder types

Other

Identifiers

NCT04664660
EndoPreg01

Details and patient eligibility

About

The purpose of this study is to assess if endometriosis can be considered a risk factor for adverse obstetric and delivery outcomes

Full description

This is a retrospective, observational, case-control study. Pregnancy, delivery and neonatal outcomes will be analyzed in two groups of patients (case and control group): women with diagnosis of endometriosis histologically confirmed and women without endometriosis. Women with endometriosis will be matched to controls by age. A database with general medical and gynecological history, pregnancy course, delivery mode and newborn conditions will be analyzed.

Enrollment

350 estimated patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Pregnant women who delivered at Azienda Ospedaliero Universitaria Policlinico di Modena from 2000 to 2020
  • Histologic diagnosis of endometriosis before pregnancy for case group
  • Age matched healthy patients for control group

Exclusion criteria

  • Clinical records not available

Trial design

350 participants in 2 patient groups

Patients with previous histologic diagnosis of endometriosis
Treatment:
Other: Retrospective analysis of obstetrics outcomes
Patient without endometriosis
Treatment:
Other: Retrospective analysis of obstetrics outcomes

Trial contacts and locations

1

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Central trial contact

Carlo Alboni

Data sourced from clinicaltrials.gov

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