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NCT06776926

Timing of Carbetocin Administration in Postpartum Hemorrhage

Completed NA Last updated 18 September 2025
What this trial tests

NA trial testing Carbetocin in Postpartum Hemorrhage in 200 participants. Completed in 28 February 2025.

Timeline
10 January 2025
Primary endpoint
28 February 2025
28 February 2025

Quick facts

Lead sponsorMehmet Mete Kırlangıç
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment200
Start date10 January 2025
Primary completion28 February 2025
Estimated completion28 February 2025
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Mehmet Mete Kırlangıç

Who can join

Adults 18 to 40, female only, with Postpartum Hemorrhage or Carbetocin. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Postpartum haemorrhage (PPH) is one of the major contributors to maternal mortality and morbidity worldwide. Active management of the third stage of labour has been proven to be effective in the prevention of PPH. Syntometrine is more effective than oxytocin but is associated with more side effects. Carbetocin, a long-acting oxytocin agonist, appears to be a promising agent for the prevention of PPH. The use of carbetocin, being an important agent in the prevention of PPH, also increases its prevalence. It is planned to investigate the advantages and disadvantages of the timing of its use.

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 Carbetocin

Trials testing the same drug.

Other recruiting trials for Postpartum Hemorrhage

Currently open trials in the same condition.

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/NCT06776926.

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