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Clinical Trials/EUCTR2012-005257-22-GB
EUCTR2012-005257-22-GB
Active, not recruiting
Phase 1

Remifentanil intravenous patient controlled analgesia (PCA) versus intramuscular pethidine for pain relief in labour: a randomised controlled trial - RESPITE

niversity of Birmingham0 sitesJune 21, 2013
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ConditionsChildbirthTherapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
DrugsRemifentanilN/A

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Childbirth
Sponsor
niversity of Birmingham
Status
Active, not recruiting
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 21, 2013
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Requesting systemic opioid analgesia
  • •16 years of age or older
  • •Beyond 30\+0 weeks’ gestation
  • •In established labour with vaginal birth intended
  • •Able to understand all information (written and oral) presented (using an interpreter if necessary) and provide signed consent.
  • •Not participating in any other clinical trial of a medicinal product
  • •Singleton pregnancy with cephalic presentation.
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range: 0
  • •F.1\.2 Adults (18\-64 years) no

Exclusion Criteria

  • •Contraindication to epidural analgesia
  • •Contraindication to intramuscular injection
  • •History of drug sensitivity to pethidine or remifentanil

Outcomes

Primary Outcomes

Not specified

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