Register study for the survey of births in patients with deep endometriosis

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00016768

Enrollment

500

Registered

2019-02-21

Start date

2019-05-25

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

N80

Interventions

Group 1: If a patient with deep endometriosis (operated or non-operated) gives birth in the participating clinics, the peripartum detalis are entered in an electronic database. The data input mask can

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: - Deep endometriosis (operated and not-operated) - Delivery - Written consent to study participation (Informed Consent)

Exclusion criteria

Exclusion criteria: - Multiple pregnancy - Abnormal fetal position

Design outcomes

Primary

Measure	Time frame
The primary outcome is the documentation of peripartal parameters of women with deep endometriosis over a longer (not yet limited) time period. The focus is on gaining information on the birth injuries, the delivery mode and the fetal outcome.	—

Countries

Austria, Germany, Switzerland

Contacts

Public ContactSimon-Hermann Enzelsberger

Kepler Universitätsklinikum - Universitätsklinik für Gynäkologie, Geburtshilfe und Gyn. Endokrinologie

simon-hermann.enzelsberger@kepleruniklinikum.at+43 5 7680 84 23718

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026