Clinical Trials Directory

Trials / Completed

CompletedNCT00816699

Effects of Providing Preprint Preoperative Anesthetic Risk Information

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
103 (actual)
Sponsor
Mahidol University · Academic / Other
Sex
All
Age
16 Years – 80 Years
Healthy volunteers
Not accepted

Summary

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

Conditions

Interventions

TypeNameDescription
OTHERpreprint preoperative anesthetic risk informationpreprint preoperative anesthetic risk information

Timeline

Start date
2008-12-01
Primary completion
2010-08-01
Completion
2010-09-01
First posted
2009-01-05
Last updated
2011-03-11

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT00816699. Inclusion in this directory is not an endorsement.

Effects of Providing Preprint Preoperative Anesthetic Risk Information (NCT00816699) · Clinical Trials Directory