Trials / Completed
CompletedNCT01490268
Pain Therapy After Elective Cardiac Surgery
Pharmacokinetic-pharmacodynamic Modeling of the Postoperative Pain Sensation During Patient-controlled Analgesia With Target-controlled Infusion of Hydromorphone, Taking Into Account the Interaction With Intraoperatively Administered Sufentanil for Elective Cardiac Surgery
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 50 (actual)
- Sponsor
- University of Erlangen-Nürnberg Medical School · Academic / Other
- Sex
- All
- Age
- 30 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine generation of a target controlled infusion model for the patient controlled analgesia with the strong analgesic, hydromorphone, after planned open heart surgery, during which the strong analgesic, sufentanil, was used.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Sufentanil, Hydromorphone | Intraoperatively: Target controlled infusion with 0.4 ng/ml Sufentanil, Postoperatively: Patient-controlled analgesia with target-controlled infusion of Hydromorphone |
| DRUG | Sufentanil, Hydromorphone | Intraoperatively: Target controlled infusion with 0.8 ng/ml Sufentanil, Postoperatively: Patient-controlled analgesia with target-controlled infusion of Hydromorphone |
Timeline
- Start date
- 2011-11-01
- Primary completion
- 2012-09-01
- Completion
- 2012-09-01
- First posted
- 2011-12-12
- Last updated
- 2014-12-08
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT01490268. Inclusion in this directory is not an endorsement.