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Clinical Trials/CTRI/2023/10/058827
CTRI/2023/10/058827
Not yet recruiting
Phase 4

Comparison of Continuous epidural infusion versus programmed intermittent epidural bolus on fetal heart rate pattern and umbilical cord blood parameters on parturients undergoing labour analgesia with Combined spinal epidural analgesia - NI

Department of Anaesthesia and Intensive Care0 sites0 target enrollmentTBD
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Overview

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

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Department of Anaesthesia and Intensive Care

Eligibility Criteria

Inclusion Criteria

  • •Full term uncomplicated pregnancy
  • •ASA I or II
  • •Primigravida
  • •Spontaneous onset of labour
  • •Cephalic presentation
  • •Singleton pregnancy
  • •Request for labour analgesia
  • •Able to use PCEA pumps

Exclusion Criteria

  • •Refusal by the parturient
  • •Obesity( \>100 kg)
  • •Parturient who had received parenteral opioids in the last 4 hours
  • •Systemic and local sepsis
  • •Deranged coagulation profile
  • •Multiple pregnancies( \>1 fetus)
  • •Obstetric complications
  • •Non\-cephalic presentation
  • •Allergy to the study drugs

Outcomes

Primary Outcomes

Not specified

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