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NCT00845390 Clinical Trial

Patient Expectations After Implantable-cardioverter Defibrillator (ICD) Implantation

Defibrillators, Implantable Clinical Trial

Official title:
Patient Expectations After ICD Implantation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00845390
Other study ID # CHR #08033561
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 2008
Est. completion date August 2009

Study information
Verified date March 2022
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will be a qualitative survey to understand the expectations of defibrillator patients with regards to their device. It is unknown what ICD (implantable-cardioverter defibrillator) patients understand about their device and its purpose, thus we will be talking to them about their device. Also, we will be interested in studying their beliefs on how the ICD impacts their life expectancy and quality of life.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date August 2009
Est. primary completion date August 2009
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - All patients are eligible for inclusion. We hope to acquire a wide range of ages but are not limited to a specific set. Exclusion Criteria: - Non-English speakers will be excluded.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States UCSF Arrhythmia and Device Clinic San Francisco California

Sponsors (1)
Lead Sponsor Collaborator
University of California, San Francisco

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Why did you have an ICD implanted? after ICD implantation
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