Clinical trial Recruiting at 2 sites Observational Ages 45 to 80

Collecting ECG data and patient insights on heart failure care

Official title: An Observational Study to Collect High Resolution 12-Lead Electrocardiogram (ECG) Data for the Development of an ECG Library to Support the Development of a Tool to Monitor Disease Progression, Gather Patient Perspectives on Standard of Care Heart Failure Procedures and Facilitate Familiarity With the Clinical Trial Environment in Patients With Heart Failure With Mildly Reduced or Preserved Ejection Fraction

Run by Richmond Pharmacology Limited · NCT06809686 · Data updated 2026-11-12

This study is collecting heart monitoring data and patient feedback from people with heart failure to help improve future heart disease research and treatments.

Quick facts

Study typeObservational
Ages45 Years to 80 Years
SexAll
Enrollment1000 (estimated)
SponsorRichmond Pharmacology Limited
Industry-sponsored
Locations2 sites (London, London and 1 other locations)
StatusRecruiting
StartedFebruary 5, 2025
Main results expectedJanuary 21, 2027
Study endsFebruary 21, 2027
Registry record updatedMay 20, 2026
Trial IDNCT06809686 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are men and women aged 45 to 80 diagnosed with heart failure with mildly reduced or preserved ejection fraction.

Probably not a fit

Patients with conditions that pose undue risk or those unable to provide informed consent may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to create a high-resolution electrocardiogram (ECG) data library to support future heart disease research. Patients with heart failure will undergo clinical assessments, and their ECGs will contribute to this library. The study also seeks to gather patient perspectives on current standard care and routine diagnostic procedures, which will inform the design of future heart failure trials. Participants may provide feedback on study designs and receive updates on new therapy options.

Why it matters

Potential benefit: If successful, this study could enhance the understanding of heart failure care and improve patient engagement in future clinical trials.

How similar studies have gone: Other studies have successfully utilized patient insights and ECG data to improve heart disease management, indicating a promising approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Male or female participants aged 45 to 80 years (inclusive) at the date of signing the informed consent.
2. Diagnosed with heart failure.
3. Able and willing to provide informed consent to participate.

Exclusion Criteria:

1. Diagnostic test results positive for:

   1. HIV-1 or HIV-2 infection
   2. Hepatitis B or Hepatitis C infection
2. Mental incapacity, language barriers or unwillingness to comply with the requirements of the protocol, which may preclude adequate understanding or cooperation during the study as judged by the Investigator.
3. Any condition judged by the Investigator to pose an undue risk while participating in the trial
4. Diagnostic results which are inconsistent with heart failure with mildly reduced or preserved ejection fraction as judged by the Investigator.

Where it's running

  • Richmond Pharmacology
    London, London, United Kingdom
    Recruiting
  • Richmond Pharmacology
    London, London, United Kingdom
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.