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Exploring the link between coronary microvascular dysfunction and heart failure with preserved ejection fraction

Elucidating the pathophysiological link between coronary microvascular dysfunction and heart failure with preserved ejection fraction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17374454
Enrollment
61
Registered
2025-03-06
Start date
2025-04-03
Completion date
Unknown
Last updated
2025-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary microvascular dysfunction (CMD) and heart failure with preserved ejection fraction (HFpEF) Circulatory System

Interventions

This study comprises an invasive and non-invasive observational arm as well as a phenotype-blinded therapeutic arm. In the observational arm, participants undergo invasive characterisation in the ca
the exercise will be supervised by a member of the research team. In the phenotype-blinded therapeutic arm, participants and researchers are blinded to the characterisation performed in the aforemen

Sponsors

King's College London
Lead Sponsor
Guy's and St Thomas' NHS Foundation Trust
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Indication for coronary angiography AND a 2. Clinical diagnosis of HFpEF

Exclusion criteria

Exclusion criteria: 1. Severe valvular disease 2. Significant epicardial coronary stenoses 3. Congenital heart disease 4. Suspected infiltrative heart disease (echo or CMR) 5. Inability to perform ambulatory, hand grip or cycle ergometric exercises 6. Pregnancy 7. Concurrent enrolment in a CTIMP trial

Design outcomes

Primary

MeasureTime frame
Ratio between the normalised delta of pulmonary capillary wedge pressure and 'exercise flow reserve' (i.e. the ratio between filling pressures and changes in coronary blood flow on exercise), measured once during the study’s invasive assessment

Secondary

MeasureTime frame
6-minute walk distance (6MWD) on anti-ischaemic treatment versus baseline, measured in metres at baseline, post 4 weeks of ranolazine administration and post 4 weeks off of ranolazine

Countries

England, United Kingdom

Contacts

Public ContactBecker Al-Khayatt
becker.al-khayatt@kcl.ac.uk+44 (0)2071887188

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026