Trials / Completed
CompletedNCT00763997
Study of the Effect of Dipyrone, Ibuprofen, Paracetamol and Parecoxib on the Platelet Aggregation in Analgetic Dosages
Study of the Effect of Dipyrone, Ibuprofen, Paracetamol and Parecoxib on the Platelet Aggregation
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Ruhr University of Bochum · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
Dipyrone is suggested to inhibit the platelet aggregation comparable to th effect of traditional analgetic substances like Ibuprofen. To verify this hypothesis the investigators conducted the study in comparing patients undergoing traumatologic, visceral or plastic surgical procedures. The investigators randomized them to four groups receiving common analgetic doses of either dipyrone, acetaminophen (paracetamol) or valdecoxib/parecoxib. The investigators took blood samples before initiation of the study drug, 1h, 4hs and 24hs after first intake. The investigators compared the aggregation via aggregometry of platelet rich plasma.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | dipyrone | Dipyrone is given in the operation room with 2,5 g intravenously, followed by an oral regime of 4x1g on the ward |
| DRUG | Ibuprofen | Ibuprofen is given orally 600mg in the Post Anesthesia Care Unit, followed by an oral regime of 800mg twice a day |
| DRUG | Acetaminophen | Acetaminophen is given 1g intravenously in the Operation room, followed by an oral regime of 1g fourth a day |
| DRUG | Acetaminophen | Acetaminophen is given 1g intravenously in the operation room, followed by 1g orally fourth a day |
| DRUG | Parecoxib/Valdecoxib | 40mg Parecoxib are given intravenously in the operation room, followed by 40mg of Valdecoxib orally twice a day |
| OTHER | Blood samples | Blood samples for aggregometry are taken before induction of anesthesia, 1h after first drug intake, 4hs and 24hs after first intake |
Timeline
- Start date
- 2004-02-01
- Primary completion
- 2004-12-01
- Completion
- 2004-12-01
- First posted
- 2008-10-01
- Last updated
- 2008-10-01
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT00763997. Inclusion in this directory is not an endorsement.