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Clinical Trials/CTRI/2022/07/044455
CTRI/2022/07/044455Not yet recruitingNot Applicable

Evaluation of postoperative analgesic effect of intraperitoneal instillation of 0.125% levobupivacaine + 1 μg/kg dexmedetomidine or 0.2% ropivacaine +1 μg/kg dexmedetomidine after laparoscopic cholecystectomy.

JLN medical college Ajmer1 site in 1 country60 target enrollmentStarted: May 8, 2022Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
1. Duration of post operative analgesia.

Study Overview

Brief Summary

We aimed to conduct a study to evaluate postoperative analgesic efficacy of intraperitoneal instillation of levobupivacaine + dexmedetomidine or ropivacaine + dexmedetomidine in patients undergoing laparoscopic cholecystectomy.

Study Design

Study Type
Interventional
Allocation
Computer generated randomization
Masking
Investigator Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •1.Patient belonging to ASA I and II 2.Gall bladder calculi.

Exclusion Criteria

  • •ASA grade III and above.
  • •age <18 years and >60 years.
  • •patients with severe systemic disease like IDDM, uncontrolled hypertension, kidney and liver disease, severe respiratory disease.
  • •seizure disorder.
  • •CAD or recent history of MI.
  • •Anticipated difficult intubation.
  • •body weight >100kg or obese.
  • •pregnant and lactating women.
  • •patient of psychiatric disorder and sleep disorders.
  • •10.hypersensitivity to study drugs.
  • •11.conversion of laparoscopic cholecystectomy to open cholecystectomy.

Outcomes

Primary Outcomes

1. Duration of post operative analgesia.

Time Frame: 1. Duration of post operative analgesia at 0,1,2,4,6,8,10,12,24 hours.

Secondary Outcomes

  • 1.total rescue analgesic required in 24 hours.(2. hemodyanamic changes.)

Investigators

Sponsor
JLN medical college Ajmer
Sponsor Class
Government medical college

Study Sites (1)

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