Overview
Effect of a Proposed Cav1.3 Inhibitor in Primary Aldosteronism
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2023-12-06
2023-12-06
Target enrollment:
0
0
Participant gender:
All
All
Summary
The goal of this pilot, open-label prospective study is to evaluate if the effect of calcium channel blockade on plasma aldosterone levels in people with primary aldosteronism (PA) is due primarily to Cav1.3 blockade. This will be tested by treating participants who have PA with both cinnarizine (Cav1.3 blocker) and nifedipine (Cav1.2 blocker) and evaluating effect on aldosterone levels and blood pressure over a two week course of treatment.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Queen Mary University of LondonTreatments:
Cinnarizine
Nifedipine
Criteria
Inclusion Criteria:- Confirmed PA, as demonstrated by a positive screening test and internationally
endorsed confirmatory test (saline suppression test, captopril challenge test)
- Adults > 18 years of age
- Able and willing to give informed consent
Exclusion Criteria:
- Uncontrolled hypertension requiring use of MRA
- Unwilling or unable to give consent
- Below age 18 or above age 90 years
- Allergy to cinnarizine or nifedipine or their excipients
- Existing use of cinnarizine or nifedipine for an alternative indication
- Breastfeeding or pregnant women
- Diagnosis of Parkinson's disease
- Severe hepatic or renal insufficiency
- Concurrent use of sedating central nervous system (CNS) depressants or rifampicin
- Porphyria
- Cardiogenic shock, clinically significant aortic stenosis, unstable angina, within one
month of a myocardial infarction
- Previous gastro-intestinal or oesophageal obstruction or ileostomy