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Clinical Trial Summary

The research was planned as a face-to-face survey evaluation. The questionnaire will be applied to obstetricians and anesthesiologists working in public and private hospitals. The universe of the research will be selected by simple random sampling method, and the total number of people who will participate is planned to be 200, approximately 100 from each of the two branches. Our survey consists of 5 parts structurally. Demographic data, rate of cesarean section and postpartum hemorrhage, uterotonic agent preferences in low/high risk cesarean section surgeries, the preference for second-line uterotonic agents, and the dose preferences of uterotonic agents.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05089721
Study type Observational
Source Gazi University
Contact
Status Enrolling by invitation
Phase
Start date November 2021
Completion date March 2022

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