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Clinical Trials/TCTR20190415001
TCTR20190415001
Enrolling By Invitation
Phase 4

Comparison of different dosage of oxytocin for initiating uterine contraction during cesarean delivery: A randomized, double-blind, controlled, non-inferiority trial

Khon Kaen University0 sites160 target enrollmentApril 15, 2019
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ConditionsAdequate uterine contraction at 3 minutesUterine contraction (verbal numerical scale 0 &#4510)Additional doses of uterotonic drugsAdditional obstetrics proceduresNausea/VomitingFlushingTachyoxytocininitiating uterine contractioncesarean delivery

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Adequate uterine contraction at 3 minutesUterine contraction (verbal numerical scale 0 &#45
Sponsor
Khon Kaen University
Enrollment
160
Status
Enrolling By Invitation
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 15, 2019
End Date
July 31, 2019
Last Updated
last year
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • •ASA physical status class II
  • •singleton pregnancy
  • •gestational age 37\-42 weeks
  • •patients were planned for cesarean delivery
  • •patients were planned for spinal anesthesia

Exclusion Criteria

  • •failed or inadequate spinal anesthesia
  • •high risk of uterine atony (macrosomia, twins, chorioamnionitis, polyhydramnios, myoma uteri)
  • •previous uterus surgery (except cesarean section)
  • •high risk of postpartum hemorrhage (placenta previa, history of previous postpatum hemorrhage, coagulopathy, thrombocytopenia, PIH)
  • •contraindication of spinal anesthesia
  • •allergy to oxytocin
  • •refuse to be volunteer

Outcomes

Primary Outcomes

Not specified

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