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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01193972
Other study ID # 10-005126
Secondary ID
Status Completed
Phase Phase 1
First received August 31, 2010
Last updated February 25, 2013
Start date September 2010
Est. completion date August 2012

Study information

Verified date February 2013
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

A decision aid tool will be developed using participatory research approach. The decision aid will be targeted to cigarette smokers scheduled for elective surgery.


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date August 2012
Est. primary completion date August 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion:

- Current cigarette smoker having elective surgery at Mayo Clinic Rochester and is scheduled to be seen at Preoperative Evaluation Center.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
Decision aid
Decision aid to assist patients in making a decision about smoking during the perioperative period

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Score on Decisional Conflict Scale and COMRADE Scale Perioperative period No
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