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Clinical Trials/NCT00816699
NCT00816699CompletedPhase 1

Effects of Providing Preprint Preoperative Anesthetic Risk Information

Mahidol University2 sites in 1 country103 target enrollmentStarted: December 2008Last updated:
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Conditions

Trial Snapshot

Phase
Phase 1
Status
Completed
Enrollment
103
Locations
2
Primary Endpoint
Spielberger State Trait Anxiety Inventory Scale
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study 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

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
16 Years to 80 Years (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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)

Investigators

Sponsor Class
Other

Study Sites (2)

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