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

Premature Rupture of Membrane Clinical Trial

Official 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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03491826
• Other study ID #: 123
• Status: Completed
• First received: March 28, 2018
• Last updated: April 6, 2018
• Start date: January 2010
• Est. completion date: December 2014

Study information

• Verified date: April 2018
• Source: Kasr El Aini Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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

Description:

The data will be retrieved from the archival files and analyzed

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1011
• Est. completion date: December 2014
• Est. primary completion date: December 2014
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 24 Years to 39 Years

Eligibility

Inclusion Criteria:

• rupture of membrane

Exclusion Criteria:

• medical disorder

Related Conditions & MeSH terms

• Fetal Membranes, Premature Rupture
• Premature Birth
• Premature Rupture of Membrane
• Rupture

Intervention

Biological:
• rupture of membrane

Locations

Country	Name	City	State
Egypt	Kasr El Ainiy Hospital	Cairo

Sponsors (2)

Lead Sponsor	Collaborator
sarah mohamed hassan	Hend Mostafa Hussein Salem

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	maternal mortality	maternal mortality	up to 48 hours after delivery