NCT00603226

Brief Summary

To compare patients with Slow Coronary Artery Flow to patients with normal flow and to determine whether there is a difference in their future incidence of heart disease.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2008

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2008

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

January 16, 2008

Completed
13 days until next milestone

First Posted

Study publicly available on registry

January 29, 2008

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2008

Completed
Last Updated

January 29, 2008

Status Verified

January 1, 2008

Enrollment Period

6 months

First QC Date

January 16, 2008

Last Update Submit

January 16, 2008

Conditions

Coronary Disease

Keywords

Coronary slow flow phenomenonCoronary angiographyAcute coronary syndromeChest painUnstable angina

Outcome Measures

Primary Outcomes (1)

  • How many hospitalizations for major coronary events in patients with or without slow coronary artery flow.

    Six months

Study Arms (2)

1

Patients diagnosed with slow coronary artery flow during coronary angiography

2

Patients with normal coronary artery flow observed during coronary angiography

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients who underwent coronary angiography in the Hillel Yaffe Medical Center

You may qualify if:

  • Patients who underwent coronary angiography

You may not qualify if:

  • Patients with coronary occulsion above 50%
  • Patients with severe valve disorder

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hillel Yaffe Medical Center

Hadera, 38100, Israel

RECRUITING

MeSH Terms

Conditions

Coronary DiseaseAcute Coronary SyndromeChest PainAngina, Unstable

Condition Hierarchy (Ancestors)

Myocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsAngina Pectoris

Study Officials

  • Yaniv Levi, MD

    Hillel Yaffe Medical Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Yaniv Levi, MD

CONTACT

972-523980951leviya@bezeqint.net

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

January 16, 2008

First Posted

January 29, 2008

Study Start

January 1, 2008

Primary Completion

July 1, 2008

Study Completion

July 1, 2008

Last Updated

January 29, 2008

Record last verified: 2008-01

Locations

IL(1)