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Clinical Trials/CTRI/2017/08/009399
CTRI/2017/08/009399
Recruiting
Phase 4

To compare the effect of intrathecal nalbuphine and fentanyl as adjuvants to bupivacaine in caesarean section.

I0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: null- Term Pregnant females undergoing caesarean section

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: null- Term Pregnant females undergoing caesarean section
Sponsor
I
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
I

Eligibility Criteria

Inclusion Criteria

  • •Term Pregnant females with ASA Grade I,II

Exclusion Criteria

  • •1\.Patientâ??s refusal
  • •2\.Any spine abnormality
  • •3\.Altered coagulation profile
  • •4\.Allergy to local anaesthetic
  • •5\.Recent myocardial infarction
  • •6\.Significant aortic stenosis
  • •Patients with neurological disorders
  • •Cardiac or respiratory system failure
  • •Any major hepatic or renal problem

Outcomes

Primary Outcomes

Not specified

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