Clinical trial Recruiting at 1 site Observational Ages 18 and up

Deciding which add-on treatments and IV furosemide doses to use for people hospitalized with heart failure

Official title: Preparatory Work for a Multi-arm, Multi-stage Trial of Adjunctive Treatments in Patients Hospitalised With Heart Failure (Pre-MAMMOTH-HF)

Run by Hull University Teaching Hospitals NHS Trust · NCT07281040 · Data updated 2026-11-12

This project will gather clinician and patient input to decide which add-on treatments, doses, and outcomes to test for people recently hospitalized with heart failure.

More Heart Failure trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment10 (estimated)
SponsorHull University Teaching Hospitals NHS Trust
Government
Locations1 site (Hull, Yorkshire)
StatusRecruiting
StartedJuly 2, 2025
Main results expectedOctober 1, 2026
Study endsOctober 1, 2026
Registry record updatedDecember 15, 2025
Trial IDNCT07281040 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

People who were hospitalized with heart failure within the past six months (or their carers) and who can take part in online group discussions in English.

Probably not a fit

Patients who were not recently hospitalized, cannot join online English discussions, or need translation/support to participate are unlikely to directly benefit from this preparatory project.

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

What this trial studies

This observational preparatory project combines an online clinician survey, a modified-Delphi expert panel, and a patient-and-carer advisory group to define the design of a future randomized trial. Clinicians (doctors, nurses, pharmacists) at sites across the UK will complete a Qualtrics survey about acceptability of adjuncts, willingness to randomize, and realistic recruitment capacity. An expert panel of ~20–25 clinicians and allied health professionals will use the evidence and a modified Delphi process to recommend adjunct selection, comparator IV furosemide doses, and primary/secondary outcomes. A patient-and-carer panel of people recently hospitalized for heart failure will advise on meaningful endpoints and acceptability of interventions.

Why it matters

Potential benefit: If successful, this work could enable a well-designed randomized trial that identifies safer or more effective add-on diuretic strategies to speed recovery and reduce rehospitalizations after heart failure hospitalization.

How similar studies have gone: Delphi panels and clinician/patient surveys are commonly used to shape trial design and endpoints and have improved relevance in other cardiovascular research, though specific adjunctive strategies for acute heart failure remain relatively under-tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Recent hospitalisation with heart failure (\<6 months) or carer for a person with a recent hospitalisation with heart failure.
2. Able to participate in online group discussions in English

Exclusion Criteria:

1\. Unable to participate in online group discussions in English

Where it's running

  • Cardiology
    Hull, Yorkshire, United Kingdom
    Recruiting

Study contacts

  • Principal investigator: Joe Cuthbert, MBBS MD — Wolfson Palliative Care Research Centre, Hull York Medical School, University of Hull, Cottingham Road, Kingston-Upon-Hull, HU6 7RX
  • Study coordinator: Joe Cuthbert, MBBS MD
  • Email: joe.cuthbert@hyms.ac.uk
  • Phone: +441482 875875

Similar studies

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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.