Status:
COMPLETED
Population PK/PD of Propofol in the Morbidly Obese Patient
Lead Sponsor:
St. Antonius Hospital
Conditions:
Morbid Obesity
Eligibility:
All Genders
18-60 years
Phase:
PHASE4
Brief Summary
Rationale: The extreme increase of obesity in the last years had led to this study. There is no consensus about how to anaesthetise morbidly obese patients. The amounts of narcotics given vary widely ...
Detailed Description
1. INTRODUCTION AND RATIONALE The extreme increase of obesity in the last years had led to this study. There is no consensus about how to anaesthetise morbidly obese patients. The amounts of narcotics...
Eligibility Criteria
Inclusion
- Patients with a Body Mass Index \> 40 undergoing laparoscopic banding or gastric bypass surgery.
Exclusion
- Epilepsy, pregnancy, breastfeeding and known allergy for Propofol, egg lecithin or soy bean oil.
Key Trial Info
Start Date :
September 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2008
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT00395681
Start Date
September 1 2007
End Date
September 1 2008
Last Update
October 22 2010
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
st. Antonius hospital
Nieuwegein, Netherlands