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Comparative Study Between Vaginal Progesterone Alone or Combined With Aspirin in Prevention of Recurrent Preterm Birth — prematurity  

Preterm Birth Clinical Trial

Official title:
Comparative Study Between Vaginal Progesterone Alone or Combined With Aspirin in Prevention of Recurrent Preterm Birth

Clinical Trial Summary

This is a double blinded randomized placebo controlled clinical trial to detect the efficacy and safety of vaginal progesterone alone or combined with aspirin in prevention of recurrent PTB.

Clinical Trial Description

The included women will be randomly allocated to prophylactically receive either vaginal progesterone at a dose of 200 mg (prontogest 200mg every 12 hr) combined with oral aspirin at a dose of 100mg once daily both at the same time (group1), or vaginal progesterone (prontogest 200mg every 12 hr) and oral placebo (manufactured in a standard way to have the same size and shape of asprin tablet) also at the same time (group 2). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05319834
Study type Interventional
Source Menoufia University
Contact
Status Completed
Phase Phase 4
Start date April 1, 2022
Completion date December 31, 2023
View Details
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