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Recruiting NCT04416958

NCT04416958 Pacing to Maintain Physiologic Ventricular Activation

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Clinical Trial Summary
NCT ID NCT04416958
Status Recruiting
Phase
Sponsor Klinikum-Fuerth
Condition Pacemaker DDD
Study Type OBSERVATIONAL
Enrollment 200 participants
Start Date 2018-01-01
Primary Completion 2025-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
cardiac implantable electronic device (CIED) implantation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 200 participants in total. It began in 2018-01-01 with a primary completion date of 2025-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Right ventricular pacing causes ventricular dyssynchrony and may be associated with impaired outcome. In the last decade, several approaches for more physiological pacing became available and were implemented in the latest guidelines. However, compared to conventional device implantation, cardiac resynchronization, His bundle pacing and left bundle area pacing remain demanding procedures in the individual case. Goal of the single center observational "Pace conduct" study is to evaluate implantation success, safety and outcome of pacing methods that maintain physiologic ventricular activation.

Eligibility Criteria

Inclusion Criteria: * Pacemaker or ICD Implantation aiming to avoid pacing induced ventricular dyssynchrony according to current guidelines * age \>= 18 years Exclusion Criteria: * no informed consent for the procedure given * no follow-up data

Contact & Investigator

Central Contact

Dirk Bastian, MD

✉ dirk.bastian@klinikum-fuerth.de

📞 +49 911 7580 1101

Principal Investigator

Dirk Bastian, MD

PRINCIPAL INVESTIGATOR

Klinikum-Fuerth

Frequently Asked Questions

Who can join the NCT04416958 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Pacemaker DDD. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04416958 currently recruiting?

Yes, NCT04416958 is actively recruiting participants. Contact the research team at dirk.bastian@klinikum-fuerth.de for enrollment information.

Where is the NCT04416958 trial being conducted?

This trial is being conducted at Fürth, Germany.

Who is sponsoring the NCT04416958 clinical trial?

NCT04416958 is sponsored by Klinikum-Fuerth. The principal investigator is Dirk Bastian, MD at Klinikum-Fuerth. The trial plans to enroll 200 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology