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Clinical Trials/CTRI/2018/05/014183
CTRI/2018/05/014183
Completed
Phase 1

To compare the functional outcome following use of local infiltration analgesia with combined spinal epidural analgesia versus combined spinal epidural analgesia alone in patients undergoing Total Knee Arthroplasty: Randomized Controlled Trial

Armed Forces Medical College Pune0 sites30 target enrollmentTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Armed Forces Medical College Pune
Enrollment
30
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
June 15, 2019
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Armed Forces Medical College Pune

Eligibility Criteria

Inclusion Criteria

  • All patients with osteoarthritis of knee undergoing unilateral Total knee arthroplasty

Exclusion Criteria

  • Patients undergoing revision knee arthroplasty, patients with peripheral vascular disease in the affected limb, patients with deranged coagulation profile, patients with major neurological deficit and uncontrolled angina, patients operated under general anesthesia, patients with history of allergy to cocktail drugs under study, patients who are provided with any alternative method of post op pain relief except combined spinal epidural analgesia.

Outcomes

Primary Outcomes

Not specified

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