Assessment Of Total Coronary Circulation Time Using TIMI Frame Count Method (TCCT-TIMI) (TCCT-TIMI)

July 10, 2016 updated by: Vascular and Molecular Cardiology Society

Assessment Of Total Coronary Circulation Time Using TIMI Frame Count Method In Patients Undergoing Coronary Angiography

The aim of this study is to evaluate and describe the total coronary circulation time (TCCT) by using TIMI frame count method in patients performed coronary angiography. TCCT is described as an angiographic index which is the sum of the frame count of coronary artery and venous system. This study also evaluates the relationship between the diseases in arterial system such as coronary artery ectasia, coronary slow flow, coronary artery disease and coronary venous pathologies.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

2000

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
      • Malatya, Turkey
        • Recruiting
        • Private Gözde Hospital
        • Contact:
          • Izzet Tandogan, MD
        • Principal Investigator:
          • Izzet Tandogan, MD
      • Mersin, Turkey
        • Recruiting
        • Private Yenisehir Hospital
        • Contact:
        • Principal Investigator:
          • Ertan Yetkin, MD
    • Kecioren
      • Ankara, Kecioren, Turkey
        • Recruiting
        • Gülhane Military Medical Academy
        • Contact:
        • Principal Investigator:
          • Turgay Celik, MD
        • Sub-Investigator:
          • Mustafa Demir, MD
        • Sub-Investigator:
          • Ali Osman Yıldırım, MD
        • Sub-Investigator:
          • Cengiz Öztürk, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patients whom performed coronary angiography with a suspicion of coronary artery disease

Exclusion Criteria:

  • History of cerebrovascular disease, chronic inflamatuar disease, malignity, chronic kidney and hepatic disease

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: Non-Randomized
  • Interventional Model: Single Group Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: normal coronary artery
coronary angiography will be performed by transfemoral or transradial route.
Procedure: coronary angiography
Coronary angiography will be performed by transfemoral or transradial approach in all patients. In order to evaluate each coronary artery, at least four views from the left and two views from the right system will be taken.
Active Comparator: coronary slow flow
coronary angiography will be performed by transfemoral or transradial route.
Procedure: coronary angiography
Coronary angiography will be performed by transfemoral or transradial approach in all patients. In order to evaluate each coronary artery, at least four views from the left and two views from the right system will be taken.
Active Comparator: coronary artery ectasia
coronary angiography will be performed by transfemoral or transradial route.
Procedure: coronary angiography
Coronary angiography will be performed by transfemoral or transradial approach in all patients. In order to evaluate each coronary artery, at least four views from the left and two views from the right system will be taken.
Active Comparator: non-obstructive coronary artery disease
coronary angiography will be performed by transfemoral or transradial route.
Procedure: coronary angiography
Coronary angiography will be performed by transfemoral or transradial approach in all patients. In order to evaluate each coronary artery, at least four views from the left and two views from the right system will be taken.
Active Comparator: obstructive coronary artery disease
coronary angiography will be performed by transfemoral or transradial route.
Procedure: coronary angiography
Coronary angiography will be performed by transfemoral or transradial approach in all patients. In order to evaluate each coronary artery, at least four views from the left and two views from the right system will be taken.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Evaluation of total coronary circulation time by using TIMI frame count method
Time Frame: 1 day
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Vascular and Molecular Cardiology Society

Collaborators

Saglik Bilimleri Universitesi Gulhane Tip Fakultesi
Private Yenisehir Hospital
Private Gozde Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2016

Primary Completion (Anticipated)

July 1, 2017

Study Completion (Anticipated)

July 1, 2017

Study Registration Dates

First Submitted

June 27, 2016

First Submitted That Met QC Criteria

June 27, 2016

First Posted (Estimate)

June 29, 2016

Study Record Updates

Last Update Posted (Estimate)

July 12, 2016

Last Update Submitted That Met QC Criteria

July 10, 2016

Last Verified

July 1, 2016

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Vasmol002

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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