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Clinical Trials/NCT00816699
NCT00816699
Completed
Phase 1

Effects of Providing Preprint Preoperative Anesthetic Risk Information

Mahidol University1 site in 1 country103 target enrollmentDecember 2008
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ConditionsPreoperative Anxiety

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Preoperative Anxiety
Sponsor
Mahidol University
Enrollment
103
Locations
1
Primary Endpoint
Spielberger State Trait Anxiety Inventory Scale
Status
Completed
Last Updated
15 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

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

Registry
clinicaltrials.gov
Start Date
December 2008
End Date
September 2010
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

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

Outcomes

Primary Outcomes

Spielberger State Trait Anxiety Inventory Scale

Time Frame: 5 days

Secondary Outcomes

  • Knowledge, proportion of patients who cancel surgery, proportion who refuse regional anesthesia(5 days)

Study Sites (1)

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