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Clinical Trials/CTRI/2017/11/010460
CTRI/2017/11/010460
Completed
未知

A prospective randomized controlled double blinded study to compare the efficacy of bilateral rectus sheath block with 0.25% bupivacaine versus local infiltration of the surgical wound with 0.25% bupivacaine in providing post-operative analgesia in patients undergoing puerperal sterilization

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Sri Ramachandra Medical College and Research Institute
Enrollment
60
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
September 12, 2016
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients coming for puerperal sterilisation belonging to American Society of Anesthesiologists Physical status Class I and II

Exclusion Criteria

  • Patients belonging to American society of Anesthesiologists Physical status class III and above
  • Infection at the site of injection
  • Coagulopathy
  • Allergy to local anesthetics

Outcomes

Primary Outcomes

Not specified

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