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Effects of Providing Preprint Preoperative Anesthetic Risk Information

Preoperative Anxiety Clinical Trial

Official title:
Effects of Providing Preprint Preoperative Anesthetic Risk Information

Clinical Trial Summary

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

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00816699
Study type Interventional
Source Mahidol University
Contact
Status Completed
Phase Phase 1/Phase 2
Start date December 2008
Completion date September 2010
View Details
See also
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