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NCT05108597

Effect of Rectal Misoprostol in Reducing Intra-operative Blood Loss During Myomectomy

Completed Phase 3 Last updated 5 November 2021
What this trial tests

Phase 3 trial testing Misoprostol in Blood Loss, Surgical in 200 participants. Completed in 4 March 2020.

Timeline
4 March 2019
Primary endpoint
4 March 2020
4 March 2020

Quick facts

Lead sponsorPak Emirates Military Hospital
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeother
Enrollment200
Start date4 March 2019
Primary completion4 March 2020
Estimated completion4 March 2020
Sites1 location across Pakistan

Drugs / interventions tested

Conditions studied

Sponsor

Pak Emirates Military Hospital

Who can join

Adults 18 to 50, female only, with Blood Loss, Surgical or Uterine Myoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A total of 200 women for elective abdominal myomectomy were randomly allocated into two groups. 100 women in experimental group were administered 400ug Misoprostol (2 tablets of Prosotec®) through the rectal route prior to surgery and 100 were in control group, in which no drug was administered.

Publications & conference data

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

Verify or expand the search:

Other trials of Misoprostol

Trials testing the same drug.

Other recruiting trials for Blood Loss, Surgical

Currently open trials in the same condition.

Other Pak Emirates Military Hospital 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/NCT05108597.

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