- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01140100
A Comparative Study of Depth of Anesthesia Monitored by Bispectral Index (BIS) Values
June 8, 2010 updated by: Shiraz University of Medical Sciences
A Comparative Study of Depth of Anesthesia Monitored by BIS Values in Two Anesthesia Techniques
The aim of this study is to determine whether induction of anesthesia with thiopental followed by propofol infusion is able to maintain sufficient depth of anesthesia .
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
82
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Fars
-
Shiraz, Fars, Iran, Islamic Republic of
- shiraz University of medical sciences
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- being adult
- having ASA I or II
- scheduled for elective cataract surgery under general anesthesia
Exclusion Criteria:
- massive obesity
- intake of any central nervous system (CNS) stimulants
- intake of CNS depressants
- intake of Tricyclic antidepressants
- known adverse reaction to the study drugs
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: propofol-propofol
|
|
Experimental: thiopental-propofol
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Sina Ghaffaripour, M.D, shiraz University of medical sciences
- Study Director: Hilda Mahmoudi, M.D, shiraz University of medical sciences
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
June 8, 2010
First Submitted That Met QC Criteria
June 8, 2010
First Posted (Estimate)
June 9, 2010
Study Record Updates
Last Update Posted (Estimate)
June 9, 2010
Last Update Submitted That Met QC Criteria
June 8, 2010
Last Verified
January 1, 2007
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 85-3211
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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