Changes in Cerebral Oxygenation During Deliberate Hypotensive Anesthesia
NCT ID: NCT00207987
Last Updated: 2007-11-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
40 participants
OBSERVATIONAL
2003-10-31
2006-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The values of cerebral oximetry and side effects between 2 groups will be compared at the completion of data collection.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Hepatic or renal impairment
* Uncontrolled hypertension
* Cardiovascular diseases
16 Years
75 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
China Medical University Hospital
OTHER
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Yu C Liu, M.D.
Role: PRINCIPAL_INVESTIGATOR
Anesthetic Department, China Medical University Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Anesthetic Department, China Medical University Hospital
Taichung, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Yu C Liu, MD
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
DMR-93-41
Identifier Type: -
Identifier Source: org_study_id