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NCT02209545

Buccal Misoprostol Prior to Abdominal Myomectomy for Reduction of Intraoperative Blood Loss: A Randomized Placebo-Controlled Trial

Terminated Phase 4 Results posted Last updated 12 August 2023
What this trial tests

Phase 4 trial testing Misoprostol in Fibroids in 47 participants. Terminated before completion.

Timeline
1 October 2014
Primary endpoint
1 July 2022
1 July 2022

Quick facts

Lead sponsorNorthwestern University
PhasePhase 4
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment47
Start date1 October 2014
Primary completion1 July 2022
Estimated completion1 July 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Northwestern University

Who can join

Adults 18 to 50, female only, with Fibroids. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The aim of this research work is to assess the impact of a single preoperative dose of buccal misoprostol in reducing blood loss during abdominal fibroid surgery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Misoprostol

Trials testing the same drug.

Other Northwestern 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/NCT02209545.

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