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Coronary Artery Disease (CAD) in Postmenopausal Women

Coronary Artery Disease in Postmenopausal Women. Comparison of Myocardial Szintigraphy With Sress-Echocardiography and Stress-MRI.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00763464
Acronym
FEMCAD
Enrollment
100
Registered
2008-10-01
Start date
2006-10-31
Completion date
2011-06-30
Last updated
2011-07-07

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

Conditions

Postmenopausal Women, Stable Angina Pectoris

Keywords

Coronary Artery Disease, ischemia diagnostic

Brief summary

Aim of this study is the determination of a valid procedure for ischemia diagnositc in postmenopausal women.

Detailed description

In order to investigate which ischemia diagnostic presents which sensitivity and specificity for postmenopausal women, 100 consecutive patients presenting to our abmulance with stable angina pectoris and indication for myocardial szintigraphy will be enrolled in this study. An addidional stress-echocardiography and stress-MRI will be performed in this patients before they will reiceve their again routine coronay angiography. The different methods for ischemia diagnostic will be compared in order to determine the most valid method for this specific population.

Interventions

stress-echocardiography will be performed once using Adenosin (140 µg/kg/min over 6 Minutes) and a contrast agent (SonoVue)

PROCEDUREstress-MRI

stress-MRI will be performed once using Adenosin (140 µg/kg/min over 6 Minutes)and a contrast agent (Gadovist)

Sponsors

RWTH Aachen University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Postmenopausal women presenting to the hospital with stable Angina pectoris complaints and an indication for myocardial szintigraphy

Exclusion criteria

* CABG * Pacemaker or other metal implants * Chronic bronchitis * Asthma bronchiale * Arterial Hypotension

Design outcomes

Primary

MeasureTime frame
comparision of different ischemia diagnostic methodsbefore routine coronary angiography

Countries

Germany

Outcome results

None listed

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