Effects of Providing Preprint Preoperative Anesthetic Risk Information

This study has been completed.
Sponsor:
Information provided by:
Mahidol University
ClinicalTrials.gov Identifier:
NCT00816699
First received: January 1, 2009
Last updated: March 10, 2011
Last verified: March 2011

January 1, 2009
March 10, 2011
December 2008
August 2010   (final data collection date for primary outcome measure)
Spielberger State Trait Anxiety Inventory Scale [ Time Frame: 5 days ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00816699 on ClinicalTrials.gov Archive Site
Knowledge, proportion of patients who cancel surgery, proportion who refuse regional anesthesia [ Time Frame: 5 days ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Effects of Providing Preprint Preoperative Anesthetic Risk Information
Effects of Providing Preprint Preoperative Anesthetic Risk Information

Proportion of patients in study group(preprint preoperative anesthetic risk should have more anxiety, more knowledge, and more cancellation than controlled group

Not Provided
Interventional
Phase 1
Phase 2
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Preoperative Anxiety
Other: preprint preoperative anesthetic risk information
preprint preoperative anesthetic risk information
  • Placebo Comparator: 1
    Routine anesthetic risk information
    Intervention: Other: preprint preoperative anesthetic risk information
  • Active Comparator: 2
    Preprint preoperative risk information
    Intervention: Other: preprint preoperative anesthetic risk information
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
103
September 2010
August 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Inpatients scheduled for surgery under general anesthesia with or without regional anesthesia
  • Low to moderate risk surgery

Exclusion Criteria:

  • Patient's refusal
  • Patients scheduled for cardiovascular surgery and neurosurgery
  • Patients with consciousness change following surgery
  • Emergency case
  • CNS or psychological diseases
Both
16 Years to 80 Years
No
Contact information is only displayed when the study is recruiting subjects
Thailand
 
NCT00816699
Si325/2008
No
Effects of providing preprint preoperative anesthetic-risk information, Faculty of Medicine Siriraj hospital, Mahidol University
Mahidol University
Not Provided
Principal Investigator: Suwannee Suraseranivongse Department of Anesthesiology, Siriraj Hospital
Principal Investigator: Suwannee Suraseranivongse, MD Department of Anesthesiology, Siriraj Hospital
Mahidol University
March 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP