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OpenTrials
Completed

NCT Number: NCT00816699

Effects of Providing Preprint Preoperative Anesthetic Risk Information

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

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Key information

Conditions

Preoperative Anxiety Anxiety Disorders Mental Disorders

Age range

16 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Faculty of Medicine, Siriraj Hospital, Mahidol Unversity

Bangkok, 10700, Thailand

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

preprint preoperative anesthetic risk information

Other

preprint preoperative anesthetic risk information

Primary outcomes

  1. Spielberger State Trait Anxiety Inventory Scale

    Time frame: 5 days

Secondary outcomes

  1. Knowledge, proportion of patients who cancel surgery, proportion who refuse regional anesthesia

    Time frame: 5 days

Sponsors and collaborators

Lead sponsor

Mahidol University

Other

Registry information

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Jan 5, 2009
Registry last updated
Mar 11, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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