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Clinical Trials/CTRI/2023/01/049329
CTRI/2023/01/049329
Completed
Phase 4

Comparison of Analgesic efficacy of continuous adductor canal block with and without IPACK block for postoperative analgesia in patients undergoing total knee replacement.

Department of Anaesthesia and Intensive Care0 sites40 target enrollmentTBD
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Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Department of Anaesthesia and Intensive Care
Enrollment
40
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
May 10, 2024
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Department of Anaesthesia and Intensive Care

Eligibility Criteria

Inclusion Criteria

  • •ASA physical status 1\-2
  • •BMI 18\-30 kg/m2
  • •Unilateral Total Knee Replacement for osteoarthritis

Exclusion Criteria

  • •Patient refusing to give informed consent.
  • •History of relevant drug allergy
  • •History of psychiatric illness, substance abuse
  • •Severe cardiovascular, respiratory , metabolic or neurological disease
  • •Pregnancy and lactation
  • •Cogaulopathy
  • •Infection at planned injection site
  • •Patient on steroids

Outcomes

Primary Outcomes

Not specified

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