Heart rate drug may keep arteries young, study suggests
NCT ID NCT02584439
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a heart-rate-lowering drug called ivabradine can improve the flexibility of arteries in healthy people. 20 volunteers with a resting heart rate of 70 or higher took either the drug or a placebo for 8 days. Researchers measured artery stiffness and other heart-related factors to see if a slower heart rate helps keep blood vessels healthy.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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20 people
The number who actually took part.
- Started
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Dec 2015
- Finished
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Jul 2019
- 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.
- Ages
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25 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Healthy volunteers * Caucasian * Resting heart rate ≥70 bpm (mean of 3 measures after 15 minutes of rest) * No significant EKG abnormality * No significant biological abnormalities at inclusion * Healthy volunteers able to read and understand information letter and to give written informed consent * Healthy volunteers with medical insurance * Contraception for two months for women of childbearing age (Estrogen contraceptive or intrauterine device or tubal ligation) (NB : women with amenorrhea for more than 2 years will be considered postmenopausal) Exclusion Criteria: * Subjects who don't understand french language * Person deprived of liberty by an administrative or judicial decision or protected adult subject (under guardianship) * Pregnant women, nursing mother or women without contraception * Healthy volunteers who participate to an other trial / participated to an other trial without drugs during the last month or a trial with drugs during the last 3 months * Hypersensitivity to the active substance or to any of the excipients * Congenital galactosemia, lactase deficiency, or glucose-galactose malabsorption * Body mass index (BMI) \< 18 kg/m² or \> 30 kg/m² * Severe hypotension (\< 90/50 mmHg) (3 measures after 15 minutes of rest) * Essential or secondary Hypertension (SBP ≥140 mmHg and/or DBP ≥90 mmHg) (3 measures after 15 minutes of rest) * Active smoking at the day of inclusion (\>5 cigarettes/day) * Severe hypercholesterolemia (Total cholesterol \>2,5 g/L) * Practice sports intensively (≥ 1 hour/day) * Renal insufficiency (creatinine clearance ≤ 60 ml/min/1,73 m² Cockroft and Gault formula) * Known liver failure * Known heart failure or suspected heart failure (congestive episode) * Atrial fibrillation * High-grade conduction block (Sick sinus syndrome, sino-atrial block or grade 2 or 3 atrio-ventricular block) * Abnormal corrected QT with Bazett formula (cQT \> 450 ms (men) or \> 470 ms (women)). * Pacemaker * All cardiac or extra cardiac diseases, active or with sequelae, which, in the opinion of the investigator, is accompanied by a risk of cardiac or vascular consequences * Retinal disease * Taking any medication is prohibited during the study except oral contraceptive, acetaminophene or decision of the investigator. In addition, the administration of drugs listed in schedule 2 during the previous 4 weeks prohibits inclusion.
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Genom att skicka in godkänner du våra Användarvillkor
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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Department of Pharmacology, Rouen university Hospital
Rouen, 76000, France
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