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WISE ARIC: Retinal Photography in Women With Chest Pain

Retinal Photography in Women With Chest Pain: A WISE/ARIC Collaboration

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00187954
Enrollment
160
Registered
2005-09-16
Start date
2003-06-30
Completion date
2014-09-30
Last updated
2021-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chest Pain

Keywords

women, chest pain, microvascular dysfunction, retinal photography, Retinal vascular function

Brief summary

The purposes of this study are: * To correlate the severity of retinal arteriolar narrowing and other microvascular changes, as determined from retinal photographs and video imaging, to measures of coronary microvascular function in women evaluated for chest pain. * To evaluate measures of vascular compliance with applanation tonometry and photoplethysmography using a nasal alar probe.

Detailed description

Women who meet study eligibility criteria and provide written informed consent will have a baseline physical exam, including measurements of heart rate, blood pressure, weight. Medical history will be updated, specifically cardiovascular events (hospitalizations, procedures) since last contact and current medications. Patients will be scheduled for retinal photography. Those who are currently being screened and qualify for EWISE or other ancillary studies will have retinal photography scheduled as close to the index CFR as possible and prior to receiving randomized therapy. The retinal photography will follow a standardized written protocol. For the second protocol, 100 patients will be scheduled for an appointment in the Eye clinic where they will meet the Women's Ischemic Syndrome Evaluation (WISE)/Atherosclerosis Risk in Communities (ARIC) staff and complete the baseline information and have a brief physical examination. They will then have provocative testing completed with retinal imaging.

Interventions

None listed

Sponsors

University of Pittsburgh
CollaboratorOTHER
University of Florida
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Women who participated in or are being screened for the WISE or EWISE or any ancillary studies * Willing to provide written informed consent * Have recorded measurements of coronary flow reserve, with or without obstructive coronary disease

Exclusion criteria

* Unwilling to complete study required procedures * Contraindication to adenosine

Design outcomes

Primary

MeasureTime frameDescription
Arteriole to venule ratio (AVR)baselineretinal arteriolar and venule diameters reflected as a ratio

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026