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Clinical Trials/CTRI/2020/02/023369
CTRI/2020/02/023369
Not yet recruiting
Phase 4

Comparison of the efficacy of the two techniques, programmed intermittent epidural boluses (PIEB) plus patient controlled epidural analgesia (PCEA) and continuous epidural infusion (CEI) plus patient controlled epidural analgesia (PCEA) on the consumption of levobupivacaine and fentanyl mixture in labouring parturients.

Department of Anaesthesia and Intensive Care0 sites0 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Department of Anaesthesia and Intensive Care
Status
Not yet recruiting
Last Updated
4 years ago

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

  • Inclusion Criteria
  • 1\.American Society of Anaesthesiologists , ASA grade 1 and grade 2
  • 2\.Age more than 18 years.
  • 3\.Primigravida.
  • 4\.Single gestation.
  • 4\.Cephalic presentation at 36 or more weeks of gestation.
  • 5\.In early spontaneous labour, cervical dilatation of 5 cm or less.
  • 6\.Baseline pain score of more than 30\.
  • 7\.Able to use PCEA pump.
  • 8\.Requesting epidural analgesia for labour.

Exclusion Criteria

  • Exclusion Criteria
  • 1\.Refusal by parturient.
  • 2\.Parturients who had recieved parenteral opiods in the last 24 hours.
  • 3\.Systemic and local sepsis.
  • 4\.Deranged coagulation profile.
  • 5\.Parturients having multiple pregnancies and premature labour.
  • 6\.Obstetric complications example premature rupture of amniotic membranes.
  • 7\.Chorioamnionitis.
  • 8\.HELLP syndrome.
  • 9\.Noncephalic presentations.

Outcomes

Primary Outcomes

Not specified

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