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Completed

NCT Number: NCT03491826

Fetal and Maternal Outcome in Preterm Premature Rupture of Membranes (PPROM)

The aim of this study is to compare fetal and maternal outcome in cases of PPROM before 34 weeks versus after 34 weeks.

Completed

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Key information

Conditions

Premature Rupture of Membrane Female Urogenital Diseases and Pregnancy Complications Fetal Membranes, Premature Rupture Obstetric Labor Complications Pregnancy Complications Urogenital Diseases

Age range

24 year–39 year

Sex eligibility

Female

Study type

Observational

Primary location

Kasr El Ainiy Hospital

Cairo, 11562, Egypt

About this study

The data will be retrieved from the archival files and analyzed

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • rupture of membrane

Exclusion criteria

  • medical disorder

Treatment and study plan

rupture of membrane

Biological

Primary outcomes

  1. maternal mortality

    Time frame: up to 48 hours after delivery

    maternal mortality

Sponsors and collaborators

Lead sponsor

sarah mohamed hassan

Other

Collaborators

  • Hend Mostafa Hussein Salem

Registry information

Official study title

Fetal and Maternal Outcome in Preterm Premature Rupture of Membranes (PPROM) at AIN Shams Maternity Hospital: A Retrospective Analysis of Last Five Years Admissions

Important dates

Study start
2010
Primary completion
2014
Study completion
2014
First posted
Apr 9, 2018
Registry last updated
Apr 9, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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