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Clinical Trials/CTRI/2013/09/003968
CTRI/2013/09/003968
Recruiting
Phase 4

Intravenous paracetamol as an adjunct to patient-controlled epidural analgesia with levobupivacaine and fentanyl in labour: a randomized controlled study

Department of anaesthesia and intensive care0 sites80 target enrollmentTBD
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Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Department of anaesthesia and intensive care
Enrollment
80
Status
Recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Department of anaesthesia and intensive care

Eligibility Criteria

Inclusion Criteria

  • •American Society of Anesthesiologists (ASA) grade I and II
  • •Age \>18 years
  • •Primigravida
  • •Single gestation
  • •Cephalic presentation at \>\= 36 wk of gestation
  • •In early spontaneous labour (cervical dilation \<\= 5 cm)
  • •Baseline pain score \> 30 (on a 0\-100 VAS)
  • •Able to use PCEA pump
  • •Requesting epidural analgesia for labour

Exclusion Criteria

  • •Refusal by parturient
  • •Parturients who had received parenteral opioids in the last 4 hours
  • •Systemic and local sepsis
  • •Deranged coagulation profile
  • •Parturients having multiple pregnancies and premature labour
  • •Obstetric complications (e.g., premature rupture of amniotic membranes)
  • •Noncephalic presentations
  • •Allergy to study drugs, i.e., paracetamol, levobupivacaine and fentanyl

Outcomes

Primary Outcomes

Not specified

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