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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05089721
Other study ID # ecd9b925a955474783d32b99b7f21
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date November 2021
Est. completion date March 2022

Study information

Verified date October 2021
Source Gazi University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 200
Est. completion date March 2022
Est. primary completion date January 2022
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: obstetricians and anesthesiologists who want to participate in the survey Exclusion Criteria: the ones who do not want to participate -

Study Design


Locations

Country Name City State
Turkey Gazi University School of Medicine Ankara

Sponsors (1)

Lead Sponsor Collaborator
Gazi University

Country where clinical trial is conducted

Turkey, 

References & Publications (1)

Thorneloe B, Carvalho JCA, Downey K, Balki M. Uterotonic drug usage in Canada: a snapshot of the practice in obstetric units of university-affiliated hospitals. Int J Obstet Anesth. 2019 Feb;37:45-51. doi: 10.1016/j.ijoa.2018.09.002. Epub 2018 Sep 12. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Uterotonic usage habits in postpartum hemorrhage to learn the uterotonic use preferences of both obstetricians and anesthesiologists in postpartum 3 months
Secondary Uterotonic usage habits in elective cesearean section to learn the uterotonic use preferences of both obstetricians and anesthesiologists in elective cesarean section 3 months
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