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Heart rate drug may keep arteries young, study suggests

NCT ID NCT02584439

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

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

Phase 3

Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.

Participants

20 people

The number who actually took part.

Started

Dec 2015

Finished

Jul 2019

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

25 to 65 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Department of Pharmacology, Rouen university Hospital

    Rouen, 76000, France

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