New blood thinner may shield heart during artery procedure
NCT ID NCT02505399
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether ticagrelor, a newer antiplatelet drug, reduces heart muscle damage during a procedure called rotational atherectomy, which clears hardened arteries. 180 stable heart patients received either ticagrelor or standard clopidogrel before and after the procedure. Researchers measured troponin levels to see if ticagrelor better prevents tiny blood clots and debris from harming the heart.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ticagrelor
- What this could lead to
- If it works, this could show that ticagrelor better protects the heart during artery-clearing procedures, potentially reducing complications.
- What could go wrong
- This is a small, completed Phase 4 trial with 180 patients, so results may not apply broadly. Ticagrelor also carries a higher bleeding risk than clopidogrel.
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.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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180 people
The number who actually took part.
- Start date
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Nov 2015
- Finished
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May 2018
- Lead sponsor
-
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.
- Ages
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18 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria : * Stable coronary patient, or patient presenting with a non ST-elevation acute coronary syndrome without troponin elevation, or with troponin back to normal, * Patient treated with a combination of Aspirin + Clopidogrel before hospitalization at the study center, * Patient with at least one highly calcified coronary lesion eligible for rotational atherectomy prior to angioplasty, * Patient agreed to participate after full information on the study. Exclusion criteria : * Acute coronary syndrome with ST-elevation, * Plasma troponin level higher than 3 times the upper limit of the laboratory, * Lesion located on a coronary bypass, * Coronary thrombus diagnosed by angiography, * Coronary dissection diagnosed by angiography, * Left ventricular ejection fraction lower than 30%, * Contra-indication to use Ticagrelor or Clopidogrel as listed in the Summary of Product Characteristics (SmPC, annex 1 \& 2): * Known hypersensitivity to the active substance or to the excipients, * Active pathological bleeding, * History of intracranial hemorrhage, * Moderate to severe hepatic impairment, * Co-administration with a strong cytochrome P450 3A4 inhibitor (e.g. ketoconazole, clarithromycin, nefazodone, ritonavir, and atazanavir), * Other conditions at increased risk of bleeding: * Congenital or acquired coagulation disorder * Gastroduodenal bleeding within past 6 months, * Recent major trauma or surgery within past 30 days, * Concomitant use of fibrinolytics, oral anticoagulation, non-steroidal antiinflammatory drugs, * Significant anemia, * Increased risk of bradycardia, * History of asthma or Chronic Obstructive Pulmonary Disease, * Uric acid nephropathy, * Ischemic stroke within 7 days, * Heredity galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption, * Concomitant use of a strong CYP3A4 inducer * Concomitant use of CYP3A4 substrates with narrow therapeutic indices (e.g. cisapride, ergot alkaloids), simvastatin at a dose greater than 40 mg/d, * Concomitant use of Selective Serotonin Reuptake inhibitors, * Concomitant use of digoxin without close clinical and laboratory monitoring, * Contra-indication to use Aspirin, * Breast-feeding, * Pregnancy, * Adult protected by the law, * Patient participating in another biomedical research.
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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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Clinique Pasteur
Toulouse, Haute-Garonne, 31000, France
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Fédération de Cardiologie CHU TOULOUSE
Toulouse, Haute-Garonne, 31059, France
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Hospices civils de Lyon
Lyon, 69000, France
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University Hospital
Nîmes, 30000, France
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