Patients Expectations for Future Examination and Treatment (TAPE)
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|ClinicalTrials.gov Identifier: NCT01551927|
Recruitment Status : Completed
First Posted : March 13, 2012
Last Update Posted : February 19, 2014
Aim: To investigate and compare women's and men's expectations before investigation and treatment of suspected coronary artery disease and to examine how these expectations are met.
Do women and men, of different ages, have the same expectations for the evaluation and treatment of stable coronary artery disease and are their expectations met in a equal degree?
Are there differences in expectations and the fulfilment of these according to age and other clinical history variables? Do the findings in the specially developed questionnaire designed to gather patients' expectations to the outcome on quality of life and degree of angina pectoris relate to their appearance in the designated forms? Is there a relationship between NTproBNP - levels, as a measure of cardiac workload, and expectations and the fulfilment of these as well as the quality of life and degree of angina pectoris?
Method: Patients will be asked to participate in the study, in the context of medical consultation before coronary angiography by a physician and / or a study nurse. This occurs during an outpatient visit at the cardiac clinic at the respective centre. Included are all patients planned for elective coronary angiography before possible revascularization during a eight month period regardless of diagnosis. Including are four hospitals in the region of Västra Götaland.
|Condition or disease|
|Coronary Heart Disease|
|Study Type :||Observational|
|Actual Enrollment :||754 participants|
|Official Title:||What Are the Expectations for Future Examination and Treatment in Patients Undergoing Evaluation and Treatment of Coronary Heart Disease?|
|Study Start Date :||March 2011|
|Actual Primary Completion Date :||January 2014|
|Actual Study Completion Date :||February 2014|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01551927
|Sahlgrenska University Hospital|
|Goteborg, Vastra Gotalands Regionen, Sweden, 41345|
|Principal Investigator:||Lars Grip, Prof||Sahlgrenska University Hospital Per Dubbscatan 15 41345 Göteborg Sweden|