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Effectiveness of Injections into the knee joint like Platelet Rich Plasma with (Hyaluronic Acid) Gel in comparison with Botulinum Toxin type A (Derived from Bacteria) with (Hyaluronic Acid) Gel in reducing Knee pain and improving function of Knee in cases of degenerative disease of Knee.

Phase 3
Conditions
Health Condition 1: M170- Bilateral primary osteoarthritis of knee
Registration Number
CTRI/2023/07/055477
Lead Sponsor
Dr Shubha V Hegde
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Bilateral Knee Osteoarthritis Grade 3 and 4.

2.Knee pain > 3 months.

3.Morning stiffness < 30 minutes.

Exclusion Criteria

1.Patient’s unwillingness to participate.

2.History of other diseases affecting knee joint like Rheumatoid Arthritis, Gout, Neuromuscular diseases.

3.Previous intra-articular injections.

4.History of knee joint surgery.

5.Acute Trauma.

6.Contraindications to intra-articular injection e.g., sepsis, intra-articular infections, intra-articular fracture, or uncontrolled coagulopathy.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.To evaluate the efficacy of intra- articular Platelet rich plasma with Hyaluronic Acid (PRP with HA) in comparison with intra- articular Botulinum Toxin A with Hyaluronic Acid on knee pain. <br/ ><br> <br/ ><br>2.To evaluate the effect of intra- articular PRP with HA in comparison with intra- articular Botulinum Toxin A with Hyaluronic Acid on functional limitation of Knee. <br/ ><br> <br/ ><br>3.To assess the effect of patient factors post procedure, on knee pain & functional limitation .Timepoint: Pre- Procedural, Immediate post procedure, 2weeks, 4 weeks, 12 weeks and 24 weeks. <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
To assess the effect of patient factors post procedure, on knee pain & functional limitation .Timepoint: Baseline, At the end of 24 weeks.
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