Clinical Trials Directory

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

TypeNameDescription
DRUGSufentanil, HydromorphoneIntraoperatively: Target controlled infusion with 0.4 ng/ml Sufentanil, Postoperatively: Patient-controlled analgesia with target-controlled infusion of Hydromorphone
DRUGSufentanil, HydromorphoneIntraoperatively: 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.