Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01248234

Does Administration of Etomidate and Propofol of the Anesthetic Induction of Elderly Hypertensive Patient Provide Superior Blood Pressure Stability in Response to Direct Laryngoscopy When Compared to Propofol or Etomidate Alone?

Does Administration of Etomidate and Propofol if the Anesthetic Induction of the Elderly Hypertensive Patient Provide Superior Blood Pressure Stability in Response to Direct Laryngosacopy, When Compared to Propofol or Etomidate Alone?

Status
Withdrawn
Phase
Phase 3
Study type
Interventional
Enrollment
0 (actual)
Sponsor
University of Mississippi Medical Center · Academic / Other
Sex
All
Age
65 Years – 90 Years
Healthy volunteers
Not accepted

Summary

This study will attempt to show that a combination of drugs, Etomidate and Propofol, provide a more stable blood pressure when used to put elderly hypertensive patients to sleep than either drug used alone.

Detailed description

Same as above.

Conditions

Interventions

TypeNameDescription
DRUGpropofolPropofol 1mg/kg will be given once to put the patient to sleep for surgery.
DRUGEtomidateEtomidate 0.3mg/kg will be given once to put the patient to sleep for surgery.
DRUGPropofol and EtomidateEtomidate 0.2mg/kg plus Propofol 0.5mg/kg will be given once to put the patient to sleep for surgery.

Timeline

Start date
2012-07-01
Primary completion
2012-07-01
Completion
2012-07-01
First posted
2010-11-25
Last updated
2012-07-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01248234. Inclusion in this directory is not an endorsement.