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Effects of Providing Preprint Preoperative Anesthetic Risk Information

NCT00816699 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 103

Last updated 2011-03-11

No results posted yet for this study

Summary

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

Conditions

  • Preoperative Anxiety

Interventions

OTHER

preprint preoperative anesthetic risk information

preprint preoperative anesthetic risk information

Sponsors & Collaborators

  • Mahidol University

    lead OTHER

Principal Investigators

  • Suwannee Suraseranivongse · Department of Anesthesiology, Siriraj Hospital

  • Suwannee Suraseranivongse, MD · Department of Anesthesiology, Siriraj Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
16 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-12-31
Primary Completion
2010-08-31
Completion
2010-09-30

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00816699 on ClinicalTrials.gov