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Clinical Trials/CTRI/2019/11/021861
CTRI/2019/11/021861
Completed
Phase 2

Randomized control trial to assess the efficacy of a single dose adductor canal block along with intra articular intermittent Ropivacaine infiltration using an epidural catheter, vs that of a Continuous adductor canal block for relief of post operative pain following Total Knee Arthroplasty

one0 sites120 target enrollmentTBD
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ConditionsHealth Condition 1: M170- Bilateral primary osteoarthritis of knee

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: M170- Bilateral primary osteoarthritis of knee
Sponsor
one
Enrollment
120
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
June 30, 2021
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
one

Eligibility Criteria

Inclusion Criteria

  • •All patients undergoing unilateral Total Knee Arthoplasty for primary osteoarthritis of the knee

Exclusion Criteria

  • •Patients undergoing bilateral surgery
  • •Patients undergoing unicondylar knee arthoplasty
  • •Patients undergoing Totalkneearthoplasty for inflammatory aetiology
  • •Patients with bleeding diathesis
  • •Patients with renalfailure/elevated renal parameters
  • •Patients with pre\-existing neuropathies
  • •Patients who have undergone any prior surgery to the affected limb

Outcomes

Primary Outcomes

Not specified

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