Clinical Trials Directory

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

TypeNameDescription
DRUGintravenous diclofenac sodium (DIC075V)intravenous diclofenac sodium
DRUGketorolacintravenous ketorolac
DRUGoral diclofenac (Cataflam)oral diclofenac (Cataflam)
DRUGaspirinoral 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.