MedDataX Logo

Diagnostic Value of HS-CRP in Stable Angina.

NCT ID: NCT00719992

Last Updated: 2008-07-22

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

97 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-04-30

Study Completion Date

2007-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim of this study was to assess the amount of additive value of HS-CRP levels to a positive exercise tolerance test (ETT) in predicting coronary artery disease (CAD) using coronary angiography as the gold standard. The investigators concluded that HS-CRP can be used as a single predictor of coronary vessel involvement in patients with stable angina and positive ETT.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

the investigators included 97 patients with positive ETT and stable angina and saw that Hs-CRP is the only predictor of severity of CAD as compared with coronary angiography in stable angina patients.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Stable Angina Positive ETT

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Exercise tolerance test HS-CRP Coronary angiography Patients

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

1

positive ETT, High HS-CRP

Group Type EXPERIMENTAL

coronary angiography

Intervention Type PROCEDURE

effect of level of HS-CRP

2

positive ETT, Low HS-CRP

Group Type ACTIVE_COMPARATOR

coronary angiography

Intervention Type PROCEDURE

effect of level of HS-CRP

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

coronary angiography

effect of level of HS-CRP

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Stable angina
* Positive ETT

Exclusion Criteria

* Unability to perform ETT
* Contraindications for ETT and angiography study
Minimum Eligible Age

43 Years

Maximum Eligible Age

64 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Shiraz University of Medical Sciences

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Shiraz University of medical sciences

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

javad kojuri, M.D.

Role: STUDY_DIRECTOR

Shiraz University of Medical Sciences

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Cardiology Ward Shiraz University of Medical Sciences

Shiraz, Fars, Iran

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Iran

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

4543

Identifier Type: -

Identifier Source: org_study_id