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NCT03741114

Foley's Catheter Balloon Plus Tranexamic Acid During Cesarean Delivery for Placenta Previa

Status unknown NA Last updated 9 January 2019
What this trial tests

NA trial testing Foley's Catheter in Placenta Previa in 120 participants. Status unknown.

Timeline
1 December 2018
Primary endpoint
30 November 2020
1 February 2021

Quick facts

Lead sponsorAswan University Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment120
Start date1 December 2018
Primary completion30 November 2020
Estimated completion1 February 2021
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Aswan University Hospital

Who can join

Adults 18 to 45, female only, with Placenta Previa. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Placenta previa (PP) is an obstetric condition that is closely linked with massive obstetric hemorrhage with a varied incidence about once in every 150-250 live births. Insertion of intrauterine balloon tamponade has been suggested in the management of massive postpartum hemorrhage (PPH). The Bakri balloon has a sausage-like spindle shape and a drainage lumen and is made of silicon. It has been used in cases of uterine atony and placenta previa with a success rate of 90%. However, Bakri balloon is not available in all countries. The aim of this study is to evaluate the efficacy of the use of intrauterine inflated Foley's catheter balloon with or without intravenous tranexamic acid to control PPH during cesarean delivery in cases of placenta previa.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Placenta Previa

Currently open trials in the same condition.

Other Aswan University Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03741114.

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