Randomized, double-blind, placebo-controlled study to compare the Efficacy of Combination of Lidocaine with Ketorolac or Triamcinolone versus Lidocaine alone for Soft Tissue Injuries Pain Management
Phase 3
Recruiting
- Conditions
- inflammation of soft tissue and efficacy of local ketorolac injectionefficacy of local injection ketorolac
- Registration Number
- TCTR20161220002
- Lead Sponsor
- RCT
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
1.age above 18 years old
2. signed inform and consent
3. diagnosis as inflammation of soft tissue
Exclusion Criteria
1.pain less than 50 in VAS
2.have NSAIDs before study less than 48 hrs
3.on probenecid,furosemide and MTX
4.infection of soft tissue and joint
5.fracture of bone
6.plan for surgery in 1 week
7.history of acute renal failure
8. age more than 65 years old
9. glaucoma
10.allergy to NSAIDs
11.peptic ulcer
12.pregnancy
13.history of diabetic
14.on anticoagulant
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain score after administration ketorolac,triamcinolone,placebo 10 min VAS score
- Secondary Outcome Measures
Name Time Method pain score after administration ketorolac,triamcinolone,placebo 30 mins 1 hr 2 hr 6 hr 24 hr VAS score,time to activity return after administration ketorolac,triamcinolone,placebo 30s min able/unable,satisfaction after administration between ketorolac,triamcinolone,placebo 2 hrs 24 hrs safisfaction score,side effect after administration between ketorolac,triamcinolone,placebo 1 wk side effec