Status:
COMPLETED
Optimizing Propofol in Obese Patients
Lead Sponsor:
Rigshospitalet, Denmark
Conditions:
Hysterectomy
Eligibility:
FEMALE
18+ years
Phase:
PHASE4
Brief Summary
An accurate dosage of anesthetics during surgery is important. Usually this is achieved through close observation of the patient, but a new monitor (CSM-monitor) can measure the level of anesthesia mo...
Eligibility Criteria
Inclusion
- Elective abdominal non-laparoscopic hysterectomy
- Age \> 18 years
- ASA physical status I-III
- Body Mass Index 30 or above
Exclusion
- Allergic towards propofol
- Daily consumption of benzodiazepines (more than at nighttime), opioids or amphetamine preoperatively.
- Disease with expected EEG-abnormality or impaired auditory function: Epilepsy, deafness, previous neurosurgery, previous or actual neurologic disease with neurologic deficit.
Key Trial Info
Start Date :
January 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2007
Estimated Enrollment :
38 Patients enrolled
Trial Details
Trial ID
NCT00270335
Start Date
January 1 2006
End Date
August 1 2007
Last Update
October 16 2009
Active Locations (2)
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1
Department of Anaesthesia, Juliane Marie Centre, Copenhagen University Hospital Rigshospitalet
Copenhagen, Denmark, DK-2100
2
Department of Anaesthesia, Copenhagen University Hospital Herlev
Herlev, Denmark, DK-2730