Effects of Providing Preprint Preoperative Anesthetic Risk Information
NCT ID: NCT00816699
Last Updated: 2011-03-11
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.
COMPLETED
PHASE1/PHASE2
103 participants
INTERVENTIONAL
2008-12-31
2010-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Reducing Low-Value Preoperative Investigations in Patients Undergoing Low Risk Surgery
NCT05526495
Multimedia Information and Pre-operative Anxiety
NCT01621828
De-implementing Low Value Preoperative Care Wisely
NCT05566327
Effect of General and Non-general Anesthesia on Perioperative Depression or Anxiety
NCT05315648
Long Term Memory Preoperative Preparation Reduce Post Operative Behavioral Change
NCT04039269
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1
Routine anesthetic risk information
preprint preoperative anesthetic risk information
preprint preoperative anesthetic risk information
2
Preprint preoperative risk information
preprint preoperative anesthetic risk information
preprint preoperative anesthetic risk information
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
preprint preoperative anesthetic risk information
preprint preoperative anesthetic risk information
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Low to moderate risk surgery
Exclusion Criteria
* Patients scheduled for cardiovascular surgery and neurosurgery
* Patients with consciousness change following surgery
* Emergency case
* CNS or psychological diseases
16 Years
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Mahidol University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Faculty of Medicine Siriraj hospital, Mahidol University
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Suwannee Suraseranivongse
Role: PRINCIPAL_INVESTIGATOR
Department of Anesthesiology, Siriraj Hospital
Suwannee Suraseranivongse, MD
Role: PRINCIPAL_INVESTIGATOR
Department of Anesthesiology, Siriraj Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Faculty of Medicine, Siriraj Hospital, Mahidol Unversity
Bangkok, , Thailand
Countries
Review the countries where the study has at least one active or historical site.
Related Links
Access external resources that provide additional context or updates about the study.
Mahidol University
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Si325/2008
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.