About this trial
The rationale for this study is that GLP-1 agonist treatment is likely to influence myocardial substrate utilisation, changing the predominant source of metabolic energy within the heart to a more energetically efficient form. This is represented by a surrogate for improved mitochondrial efficiency with reduction in myocardial lactate levels (produced by inefficient myocardial glycolysis, prevalent in the ventricles of patients with pulmonary hypertension), which can be measured by 31P-magnetic resonance spectroscopy (31P-MRS).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
• 1. Pregnancy
2. Myocardial infarction within the previous 3 months
3. Contraindications to MRI: Pacemakers, metallic implants, or severe claustrophobia.
4. Severe renal impairment: eGFR < 15ml/min/1.73m.
Trial design
Single group
Treatments tested in this trial
GLP-1 agonist
DrugSemaglutide
Treatment groups
Trial outcomes
Primary outcomes
Change in the phosphocreatine-to-adenosine triphosphate (31PCr/ATP) ratio between baseline and follow up in response to treatment with GLP-1 agonist
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: