Current partner codePEPTIDESDE
NCT06946589·Phase 4·INTERVENTIONAL

Cardiac Changes After Effective Dose Carbetocin for Elective Caesarian Section

Status

Not yet recruiting

Phase

Phase 4

Enrollment

200

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

The goal of this project is to examine the cardiac symptoms and physiologic changes after administration of a reduced dose of carbetocin in participants undergoing elective cesarian section. * Does reduced dose carbetocin (50mcg) have fewer cardiac side effects than usual dose carbetocin (100mcg) when comparing patient reported symptoms, ECG changes and troponin increases? * Is there a relationship between patient reported cardiac symptoms after carbetocin administration and subjective measures of cardiac ischemia (ECG changes and troponin increases? Researchers will compare 50mcg of carbetocin to the control group of 100mcg of carbetocin in patients undergoing elective cesarian section. Participants will: * Be given 50mcg or 100mcg of carbetocin during cesarian section * Asked to report cardiac symptoms * Be assessed for ECG changes and blood loss using standard of practice monitoring * Have a troponin I blood test completed after delivery

Interventions

Treatment arms and agents.

DRUG

Carbetocin

A uterotonic agent used for the prevention of postpartum hemorrhage in Cesarian section

Timeline

From registration to results.

  1. First posted

    Apr 27, 2025

  2. Study start

    Aug 1, 2025

  3. Primary completion

    Aug 1, 2026

  4. Study completion

    Sep 1, 2027

  5. Results posted

    Not reported

  6. Registry updated

    Apr 27, 2025

Outcomes

What the study measures.

Primary outcomes

Patient reported symptoms

Time frame · within 5 minutes of study drug administration

Subjective patient reported symptoms of cardiac ischemia, reported with descriptive words

Secondary outcomes

Troponin I levels

Time frame · One day after study drug administration

Troponin I levels on blood work

ECG: ST segment

Time frame · 5 minutes after study drug administration

Changes to the ST segment on ECG

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
FEMALE
Healthy volunteers
No

Inclusion Criteria: * Undergoing elective cesarian section * Primary and repeat cesarian section Exclusion Criteria: * Prior and current cardiovascular co-morbidities including pre-eclampsia * BMI greater than 50 * Pre-existing bleeding disorders * Allergy to carbetocin * Age under 18

Study locations

1 registered sites.

Canada. Showing up to 24 locations stored in the fast local snapshot.

Kingston Health Sciences Centre

Kingston, Ontario, Canada

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Carbetocin.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.