MedPath

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 injection
efficacy 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
NameTimeMethod
pain score after administration ketorolac,triamcinolone,placebo 10 min VAS score
Secondary Outcome Measures
NameTimeMethod
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
© Copyright 2025. All Rights Reserved by MedPath