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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01248234
Other study ID # 2010-0097
Secondary ID
Status Withdrawn
Phase Phase 3
First received November 23, 2010
Last updated July 12, 2012
Start date July 2012
Est. completion date July 2012

Study information

Verified date July 2012
Source University of Mississippi Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial 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.


Description:

Same as above.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 2012
Est. primary completion date July 2012
Accepts healthy volunteers No
Gender Both
Age group 65 Years to 90 Years
Eligibility Inclusion Criteria:

- Patients at least 65 years old, with a history of hypertension.

Exclusion Criteria:

- Patients less than 65 years old or without a history of hypertension.

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Drug:
propofol
Propofol 1mg/kg will be given once to put the patient to sleep for surgery.
Etomidate
Etomidate 0.3mg/kg will be given once to put the patient to sleep for surgery.
Propofol and Etomidate
Etomidate 0.2mg/kg plus Propofol 0.5mg/kg will be given once to put the patient to sleep for surgery.

Locations

Country Name City State
United States University of Mississippi Medical Center Jackson Mississippi

Sponsors (1)

Lead Sponsor Collaborator
University of Mississippi Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood pressure stability during anesthetic induction Blood pressure will be measures every minute for 15 minutes following anesthetic induction 15 minutes Yes
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