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Clinical Trials/TCTR20220215009
TCTR20220215009
Unknown
Phase 4

Subcutaneous versus intravenous fentanyl for labor pain management A multicenter randomized controlled trial

Khon Kaen University0 sites226 target enrollmentFebruary 15, 2022

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Pregnant women who plan vaginal delivery and have labor pain at 37-41+6 weeks of gestation
Sponsor
Khon Kaen University
Enrollment
226
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 15, 2022
End Date
March 1, 2023
Last Updated
last year
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\.pregnant women who 18 years old or older
  • 2\. gestational age between 37 \- 41 weeks 6 days
  • 2\. plan vaginal delivery
  • 3\. singleton pregnancy with cephalic presentation
  • 4\. no obstetric or medical complication
  • 5\. require medication for labor pain relief
  • 6\. cervix open 4\-9cm.

Exclusion Criteria

  • 1\. pregnant women who have fetal anomaly
  • 2\. pregnant women who receive pethidine or morphine 24 hour prior
  • 3\. pregnant women who addict opioid drugs
  • 4\. pregnant women who receive any psychosis drugs 14 days prior admission
  • 5\. pregnant women who have epilepsy and on enzyme CYP 3A4 inducers drugs such as carbamazepine, phenytoin ,rifampin
  • 6\. pregnant women who have underlying disease such as liver disease heart disease respiratory tract infection
  • 7\. pregnant women who do not understand Thai language

Outcomes

Primary Outcomes

Not specified

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