Last reviewed · How we verify

NCT03723031

Intrauterine Misoprostol Versus Rectal Misoprostol in Reducing Blood Loss During Cesarean Section

Status unknown Phase 2 Last updated 18 March 2020
What this trial tests

Phase 2 trial testing Misoprostol in Hemorrhage, Postpartum in 98 participants. Status unknown.

Timeline
15 November 2018
Primary endpoint
15 April 2020
15 May 2020

Quick facts

Lead sponsorCairo University
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeprevention
Enrollment98
Start date15 November 2018
Primary completion15 April 2020
Estimated completion15 May 2020
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Cairo University

Who can join

Adults 20 to 40, female only, with Hemorrhage, Postpartum. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

98 pregnant women attending for CS will be randomized into 2 groups. Rectal misopristol group who will receive 400 microgram misoprostol rectally preoperatively with urinary catheter insertion and intrauterine misopristol group will receive 400 microgram misoprostol intrauterine (200 microgram at each cornu) intraoperatively following the delivery of the placenta. The estimated blood loss for each patient will be measured and data of both groups will be compared.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. A comparative study between preoperative rectal misoprostol and intraoperative intrauterine administration in the reduction of blood loss during and after cesarean delivery: A randomized controlled trial.
    El-Sherbini MM, Maged AM, Helal OM, Awad MO, et al · · 2021 · cited 5× · PMID 33064852 · DOI 10.1002/ijgo.13426

Verify or expand the search:

Other trials of Misoprostol

Trials testing the same drug.

Other recruiting trials for Hemorrhage, Postpartum

Currently open trials in the same condition.

Other Cairo University trials

Trials by the same sponsor.

Verify against primary sources

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/NCT03723031.

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