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OpenTrials
Completed

NCT Number: NCT01170988

Coronary Flow Rate Measurement in T-Grafts

Is the surgical treatment of patients with coronary heart disease using the T-graft technique an adequate solution that provides a sufficient myocardial flow reserve? A magnetic resonance examination (MRI) is required.

Completed

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Key information

Age range

18 year–80 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Johann Wolfgang Goethe Universitätsklinikum

Frankfurt am Main, 60590, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • coronary heart disease
  • Age > 18 ys
  • Ejection fraction > 45%

Exclusion criteria

  • myocardial infarction
  • Re-Intervention

Treatment and study plan

T-Graft

Procedure

T-Graft

Primary outcomes

  1. Coronary flow reserve

    Time frame: within 4-6 weeks

Sponsors and collaborators

Lead sponsor

Johann Wolfgang Goethe University Hospital

Other

Collaborators

  • Bethanien Krankenhaus gGmbH

Registry information

Official study title

Comparison of Coronary Flow Reserve in Two Different Bypass Techniques (T-graft Technique Versus Isolated Graft Technique) Using Magnetic Resonance Technology (MRT)

Important dates

Study start
2010
Primary completion
2014
Study completion
2014
First posted
Jul 28, 2010
Registry last updated
Aug 6, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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