Evaluation of the effectiveness of oral Aspirin in reducing complex regional pain syndrome (CRPS)
Phase 3
- Conditions
- Condition 1: Complex regional pain syndrome. Condition 2: distal radius fracture.Complex regional pain syndrome I (CRPS I)Fracture at wrist and hand level
- Registration Number
- IRCT20180116038391N1
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
closed, unilateral, extra-articular distal radius fracture
eighteen years and over
Exclusion Criteria
history of taking medications that were involved in the treatment of CRPS (such as antidepressants, anticonvulsants, corticosteroids and vitamin C)
previous wrist or hand fracture on the same side
neurovascular injury
fractures with high energy mechanism or multiple trauma-injured patients, multiple fractures at different places
contraindication to take aspirin and acetaminophen
open fractures
articular displacement requiring open reduction
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Complex regional pain syndrome. Timepoint: 2, 4, 6 and 12 week post operation. Method of measurement: Budapest’s criteria.
- Secondary Outcome Measures
Name Time Method