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Clinical Trial Summary

The investigators are investigating whether slow administration of carbetocin is tolerated by patients better than if it is administered quickly, with respect to side effects such as headache, nausea, vomiting and facial flushing.


Clinical Trial Description

Patients undergoing elective cesarean under spinal are included in the study. These patients are treated with carbetocin to reduce blood loss from the lining of the womb after delivery of the baby. The study is a randomised double blind controlled trial with 2 groups. One group will receive carbetocin quickly, the second group will receive carbetocin slowly. The investigators will compare the difference between groups with respect to side effects and the effect of carbetocin on the cardiovascular system. ;


Study Design


Related Conditions & MeSH terms

  • Effect of Carbetocin on Cardiovascular System
  • Pregnancy

NCT number NCT02636816
Study type Interventional
Source University of British Columbia
Contact
Status Completed
Phase Phase 4
Start date March 2016
Completion date June 2016

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