MedPath

Comparison of local infiltration analgesia and epidural analgesia in postoperative pain management, functional outcomes and blood loss control in total knee arthroplasty

Phase 3
Recruiting
Conditions
Osteoarthritis of Knee.
Osteoarthritis of Knee
Registration Number
IRCT20170807035554N1
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

50 - 85 years old with knee pain
Don't response to conservative treatment

Exclusion Criteria

TKA revision
Bilateral TKA
Collagen vascular disease
Neurovascular disease
Hematologic disease
Coagulopathy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ROM Bleeding SLR Pain. Timepoint: 2 Days & 2 Weeks. Method of measurement: A questionnaire based on VAS-Score.
Secondary Outcome Measures
NameTimeMethod
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