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Clinical Trials/CTRI/2019/08/020837
CTRI/2019/08/020837
Completed
Phase 1

A prospective randomised double blinded controlled study to assess the efficacy of intraperitoneal 0.25% levobupivacaine for postoperative analgesia following laparoscopic cholecystectomy

Pavithra Palaniappan0 sites56 target enrollmentTBD
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ConditionsHealth Condition 1: K00-K95- Diseases of the digestive system

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Health Condition 1: K00-K95- Diseases of the digestive system
Sponsor
Pavithra Palaniappan
Enrollment
56
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
February 12, 2020
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Pavithra Palaniappan

Eligibility Criteria

Inclusion Criteria

  • •Patients undergoing laparoscopic cholecystectomy
  • •Patients of ASA1 and ASA 2

Exclusion Criteria

  • •Patients allergic to local anaesthetics
  • •Patients with severe cardiac, pulmonary, and neurological disease
  • •Patients in whom procedure has to be converted to open cholecystectomy
  • •Patients in whom abdominal drain will be kept
  • •Patients of weight less than 50 kg
  • •Patients not willing to participate

Outcomes

Primary Outcomes

Not specified

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