Heart stent study halted early: can a pressure wire improve outcomes?
NCT ID NCT02797561
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at using a special wire that measures blood pressure inside heart arteries (called FFR) to help doctors decide which blockages to treat with stents. It included 438 people with two or more blockages in the same artery. The study was stopped early, so the results are not complete, but the goal was to see if FFR guidance reduces heart-related deaths, heart attacks, or the need for repeat procedures.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Fractional flow reserve (FFR) measurement during stent placement
- What this could lead to
- If successful, this could show that FFR guidance helps doctors decide which blockages to treat, potentially reducing heart attacks and repeat procedures.
- What could go wrong
- The study was terminated early, so results are limited. It was observational, not a randomized trial, so it cannot prove cause and effect.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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438 people
The number who actually took part.
- Started
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Jul 2016
- Finished
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Apr 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
patients with tandem lesion evaluated by FFR
- Ages
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19 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Tandem lesion evaluated by FFR * Written consent Exclusion Criteria: * TIMI flow \< 3 * Grafted vessel * Left ventricular ejection fraction \< 30% * Severe calcification and/or severe tortuosity * Uncontrolled coronary spasm * Life expectancy \< 2 years * Planned high risk surgery * Pregnancy or breast-feeding
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Asan Medical Center
Seoul, Songpa-gu, 138-736, South Korea
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Bundang CHA Hospital
Seongnam, South Korea
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Chungnam National University Hospital
Daejeon, South Korea
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Daegu Catholic University Medical Center
Daegu, South Korea
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Gangwon National Univ. Hospital
Chuncheon, South Korea
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Inje University Ilsan Paik Hospital
Ilsan, South Korea
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Keimyung University Dongsan Medical Center
Daegu, South Korea
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Pusan National University Yangsan Hospital
Yangsan, South Korea
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Seoul National University Bundang hospital
Seongnam, South Korea
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Seoul National University hospital
Seoul, South Korea
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Soon Chun Hyang University Hospital Bucheon
Bucheon-si, South Korea
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Wonju Severance Christian Hospital
Wŏnju, South Korea
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