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NCT04807543

Effect of Progesterone on Latent Phase Prolongation in Patients With Preterm Premature Rupture of Membranes

Completed Phase 2 Last updated 19 March 2021
What this trial tests

Phase 2 trial testing 17-hydroxyprogesterone caproate in Preterm Premature Rupture of Membrane in 100 participants. Completed in 10 December 2020.

Timeline
10 January 2018
Primary endpoint
10 October 2020
10 December 2020

Quick facts

Lead sponsorAin Shams University
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposesupportive care
Enrollment100
Start date10 January 2018
Primary completion10 October 2020
Estimated completion10 December 2020
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Ain Shams University

Who can join

Adults 20 to 35, female only, with Preterm Premature Rupture of Membrane. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the study is to assess the efficacy of 17-hydroxyprogesterone caproate (17P) therapy on the latency period in pregnant women with Preterm premature rupture of membranes.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Preterm Premature Rupture of Membrane

Currently open trials in the same condition.

Other Ain Shams University trials

Trials by the same sponsor.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing