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

M

Maisonneuve-Rosemont Hospital

Status

Completed

Conditions

Cesarean Section Complications
Carbetocin
Uterine Atony With Hemorrhage
Uterotonics

Treatments

Drug: Carbetocin

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT03959436
2017-836

Details and patient eligibility

About

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.

Enrollment

612 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All Cesarean deliveries in the operating room.

Exclusion criteria

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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