Efficacy and safety of intra-articular botulinum toxin A versus corticosteroid injections in knee osteoarthritis: A randomised control trial
- Conditions
- Knee osteoarthritisMusculoskeletal - OsteoarthritisAnaesthesiology - Pain management
- Registration Number
- ACTRN12621001622897
- Lead Sponsor
- Stephanie Babic
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 100
1.Age more than or equal to 40 years.
2.Diagnosis of knee OA confirmed on clinical exam and radiologically by Kellgren-Lawrence Grading Scale (Grade III or IV);
3.Symptoms present for more than or equal to 6 months; and
4.Ability to understand and participate in the trial.
1.Age less than 40 years;
2.Any intra-articular injection within the past 12 months;
3.History of trauma to the knee within the past 12 months;
4.History of surgery to the knee within the past 12 months;
5.Neuromuscular disorders (for example, myasthenia gravis, Lambert-Eaton, amyotrophic lateral sclerosis et cetera);
6.Other knee arthropathy (for example, RA, gout et cetera);
7.Lower extremity dysfunction due to a neurological or medical cause (for example, due to a cerebrovascular accident or traumatic brain injury, diabetic neuropathy et cetera);
8.Serious coagulation disorders or anticoagulant use; and
9.Pregnancy or breastfeeding.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method