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OpenTrials
Completed

NCT Number: NCT03959436

Database Evaluating Outcomes of Using Carbetocin as the Primary Uterotonic Following Cesarean Delivery

Carbetocin (Duratocin®) is a long-acting form of oxytocin, with a half-life almost 10 times longer. Studies have demonstrated that carbetocin diminishes the need for secondary uterotonic agents compared to oxytocin for cesarean delivery (CD). Despite certain Canadian guidelines recommending its use for elective CD, several Canadian centers and other countries have not adopted carbetocin. The purpose of this study is to prospectively gather electronic data on all CDs over a one year period, elective and emergent, in a single institution, and to evaluate the efficacy and other clinical outcomes when carbetocin is used as a first line uterotonic for all CDs. A database using Microsoft Dynamics CRM is available on smart phones and tablets. Data regarding additional uterotonic use and impact of carbetocin use during CD on intra and postoperative outcomes are gathered and analyzed. The primary outcome is the use of additional uterotonics in this population compared to that described in the literature for oxytocin as the primary uterotonic.

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Key information

Sex eligibility

Female

Study type

Observational

Primary location

Maisonneuve-Rosemont hospital

Montreal, Quebec, H1T 2M4, Canada

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All Cesarean deliveries in the operating room.

Exclusion criteria

  • Vaginal deliveries and double set-up vaginal deliveries conducted in the operating room.

Treatment and study plan

Carbetocin

Drug

Carbetocin as the primary uterotonic for all cesarean sections

Other names: Duratocin

Primary outcomes

  1. Use of additional uterotonics

    Time frame: 24 hours

    The number of participants requiring additional uterotonics after using carbetocin as the initial uterotonic

Sponsors and collaborators

Lead sponsor

Maisonneuve-Rosemont Hospital

Other

Collaborators

  • Ferring Pharmaceuticals

Registry information

Official study title

Prospective Observational Database Evaluating Outcomes of Using Carbetocin (Duratocin®) as the Primary Uterotonic Following Cesarean Delivery at Maisonneuve-Rosemont Hospital

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
May 22, 2019
Registry last updated
May 29, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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