Heart Failure Clinical Trials

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

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

Aims and Objectives 1. Choose which adjunctive therapies, at what dose, and for how long 2. Choose the dose(s) of IV furosemide to be used as the comparator 3. Choose primary and secondary outcomes 4. Estimate recruitment and engage sites for a future trial Work package 2a methods overview 1. An online survey of clinicians (doctors, nurses and pharmacists) assessing potential ability to recruit and the acceptability of each adjunct and willingness to support a trial. 2. Evidence generated (survey and reviews) will be considered by an expert panel (N=20-25) including expert clinicians and allied health professionals who care for people with HF using a modified Delphi approach. The panel will make recommendations on all aspects of the trial design. 3. A patient and carer panel of people with a recent hospitalisation (\<6 months) for HF will provide recommendations on trial endpoints. The patient-and-carer advisory group (PCAG) will also input into these discussions.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Recent hospitalisation with heart failure (\<6 months) or carer for a person with a recent hospitalisation with heart failure.

• Able to participate in online group discussions in English

Locations
Other Locations
United Kingdom
Cardiology
RECRUITING
Hull
Contact Information
Primary
Joe Cuthbert, MBBS MD
joe.cuthbert@hyms.ac.uk
+441482 875875
Time Frame
Start Date: 2025-07-02
Estimated Completion Date: 2026-10-01
Participants
Target number of participants: 10
Related Therapeutic Areas
Sponsors
Collaborators: Robertson Centre for Biostatistics University of Glasgow Glasgow G12 8QQ, University of Birmingham, Hull York Medical School
Leads: Hull University Teaching Hospitals NHS Trust

This content was sourced from clinicaltrials.gov