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COMPARISON OF TWO COMBINED NERVE BLOCKS FOR POSTOPERATIVE PAIN RELIEFE IN TOTAL KNEE REPLACEMENT

Phase 4
Conditions
Health Condition 1: M179- Osteoarthritis of knee, unspecified
Registration Number
CTRI/2024/08/071958
Lead Sponsor
Government Medical College Baroda
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Age group- 40-85 yr

Either sex

ASA –I II III

Patient posted for elective Total knee Arthroplasty.

Patient able to give verbal and informed consent.

Patient able to understand VAS regarding assessment of pain

Exclusion Criteria

Patient refusal

Allergy to local anesthetics.

Patient with local site infection

Patient with coagulopathy disorder

Patient with cognitive and psychiatric illness

Patient with peripheral neuropathy and neurological deficit

Patient with severe cardiovascular, respiratory, renal and

hepatic disease (ASA-IV)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Duration of analgesia using VAS scoreTimepoint: till 24 hr
Secondary Outcome Measures
NameTimeMethod
umber of rescue analgesia required in 24 hrs <br/ ><br>Degree of active knee flexion at 20 hr and 24 hr post procedural using goniometer <br/ ><br> Extent of motor blockage using Modified Bromage scale <br/ ><br>Post procedural Hemodynamics <br/ ><br>Complications like Nerve injury, Hematoma, local anaesthetic systemic toxicity.Timepoint: till 24 hr
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