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Clinical Trials/IRCT20230403057808N1
IRCT20230403057808N1
Recruiting
Phase 3

Comparison of intrathecal injection of fentanyl and sufentanil along with bupivacaine in the onset, duration and quality of painless labor; A randomized double-blind clinical trial

Rasht University of Medical Sciences0 sites80 target enrollmentTBD
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Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Rasht University of Medical Sciences
Enrollment
80
Status
Recruiting
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Rasht University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • •Primiparous or multiparous pregnant mothers with term pregnancy
  • •Single fetus
  • •American Society of Anesthesiologists' (ASA) classification I, II
  • •In the advanced stage of labor with cervical dilation at least 5 centimeter in Primiparous and at least 4 centimeter in multiparous mothers
  • •Age more than 18 years
  • •Tending to have painless labor

Exclusion Criteria

  • •Refusal to participate in the study by pregnant mothers
  • •Endocrine disease
  • •Allergy to study drugs
  • •Regional anesthesia contraindications such as coagulopathy, high intracranial pressure and infection of injection site .

Outcomes

Primary Outcomes

Not specified

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