Trials / Completed
CompletedNCT00548678
Platelet Function and Safety After IV and Oral Diclofenac, IV Ketorolac and Oral Aspirin in Adult Volunteers
Open-Label, Randomized, Single-Dose, Four-Treatment Crossover Study to Evaluate Platelet Function in Healthy Adult Males After Administration of IV Diclofenac Sodium, Oral Diclofenac Potasssium, IV Ketorolac Tromethamine, and Acetylsalicylic Acid
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- Javelin Pharmaceuticals · Industry
- Sex
- Male
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Accepted
Summary
This study will assess platelet function and safety in healthy male volunteers following doses of intravenous diclofenac compared to oral diclofenac (Cataflam), intravenous ketorolac and oral aspirin.
Detailed description
The primary objective is to evaluate platelet function following intravenous diclofenac, oral diclofenac (Cataflam), intravenous ketorolac and oral aspirin.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | intravenous diclofenac sodium (DIC075V) | intravenous diclofenac sodium |
| DRUG | ketorolac | intravenous ketorolac |
| DRUG | oral diclofenac (Cataflam) | oral diclofenac (Cataflam) |
| DRUG | aspirin | oral aspirin |
Timeline
- Start date
- 2007-10-01
- Primary completion
- 2007-11-01
- Completion
- 2007-11-01
- First posted
- 2007-10-24
- Last updated
- 2008-07-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00548678. Inclusion in this directory is not an endorsement.