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New disinfectant may slash heart device infections

NCT ID NCT04735666

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 This study
Running, but no longer taking on new participants.
Completed
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 is testing whether using a disinfectant called TauroPace during heart device surgery can prevent infections. About 2300 patients having procedures like pacemaker placement or replacement are being followed for up to 12 months. The goal is to see if this approach reduces the risk of serious infections around the device.

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

About 2,300 people

The number the study aims to enrol. It can still change while the study runs.

Started

Feb 2021

Expected to finish

Jan 2030

An estimate. End dates often move.

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.

Who is studied

The study population consist of every subsequent participant eligible for any CIED related surgery with TauroPace™

Ages

18 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Use of TauroPace™ is indicated and not contra-indicated according to its current Instructions For Use (IFU) * Participant is eligible for a CIED related surgery procedure. Exclusion Criteria: * Age\<18years * Participant incapable of signing Patient Informed Consent (mentally or physically) or does not sign.

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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

  • Great Western Hospitals NHS Foundation Trust

    Swindon, SN3 6BB, United Kingdom

  • Helios Klinik Cuxhaven

    Cuxhaven, Lower Saxony, 27474, Germany

  • Helios Klinik Wesermarsch

    Nordenham, Lower Saxony, 26954, Germany

  • Krankenhaus Landshut Achdorf

    Landshut, Bavaria, 84036, Germany

  • Landeskrankenhaus Wiener Neustadt

    Wiener Neustadt, 2700, Austria

  • Louis Pradel Hospital

    Lyon, Bron, 69500, France

  • Ospedale Regionale San Maurizio

    Bolzano, Trentino-Alto Adige, 39100, Italy

  • University Hospital Schleswig-Holstein

    Kiel, Schleswig-Holstein, 24105, Germany