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When is the best time to give carbetocin to stop postpartum bleeding?

NCT ID NCT06776926

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This completed trial studied 200 first-time mothers having a normal vaginal delivery to find the best time to give carbetocin, a drug that prevents severe bleeding after childbirth. Researchers compared giving the drug at different times to see which reduced bleeding, side effects, and the need for extra medications. The goal is to improve safety during childbirth.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
carbetocin
What this could lead to
If successful, this could help doctors choose the best time to give carbetocin to prevent dangerous bleeding after childbirth.
What could go wrong
This is a small, completed trial with 200 participants, so results may not apply to all women. The timing difference may not be significant.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

200 people

The number who actually took part.

Started

Jan 2025

Finished

Feb 2025

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 40 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Singleton pregnancy * Vaginal delivery at or beyond 38 weeks of gestation * Primipar Exclusion Criteria: * Multiparity * Contraindications to carbetocin use (e.g., pre-existing hypertension, pre-eclampsia,asthma, cardiac, renal, or liver disease) * High-risk factors for primary postpartum hemorrhage, including grand multiparity,presence of uterine fibroids, or a need for prophylactic oxytocin infusion * Anemia or * body mass index (BMI) over 35 * Baby weight over 4000 grams * Comorbidities or chronic diseases * History of curettage * Use of propess or oxytocin during labor

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Conditions

The condition(s) this trial relates to.

Placenta, Retained Postpartum Hemorrhage

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Kartal Dr Lutfi Kirdar City Hospital

    Istanbul, Istanbul, 34880, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.