Quality of Life in Patients With Refractory Angina

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

90 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-12-31

Study Completion Date

2013-12-31

Brief Summary

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The health and well being of patients with refractory angina will be assessed using validated questionnaires (SF-36 and Seattle Angina Questionnaire \[SAQ\]) at baseline and one year.

Detailed Description

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Conditions

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Refractory Ischemia

Keywords

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angina health related quality of life

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* In the OPTIMIST clinic with documented refractory angina
* Have consented to participate in the OPTIMIST Long-term Follow-up Database

Exclusion Criteria

* Decline to participate or are unwilling to give written consent

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Timothy D Henry, MD

Role: PRINCIPAL_INVESTIGATOR

Minneapolis Heart Institute Foundation

Locations

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Abbott Northwestern Hospital

Minneapolis, Minnesota, United States

Site Status

Countries

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United States

Other Identifiers

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opt003

Identifier Type: -

Identifier Source: org_study_id