Trials / Unknown
UnknownNCT00429897
Double Blind Crossover Comparison of Diuretics in the Young
Double Blind Crossover Comparison od Diuretics in Young Patients With Low Renin Hypertension
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 30 (planned)
- Sponsor
- University of Cambridge · Academic / Other
- Sex
- All
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Not accepted
Summary
The principle objective of the study is to determine whether low-renin (i.e. salt sensitive) hypertension at a young age is caused by the kidneys hanging onto too much salt as a result of an over active salt pump in the kidney. The kidneys have four different salt pumps, and each is blocked by a different type of diuretic (salt losing tablet)If one out of the four is overactive, we would expect patients to respond much better to one diuretic than to the alternatives - rather than responding equally well to all available types of diuretic.
Detailed description
Studies suggest that patients with low renin hypertension respond better to diuretics than other hypertensive drug groups. The aim of the study is to rotate patients through the four main diuretic groups and see if it is possible to identify the most effective diuretic for this group, as measured by a \>=10mgHg decrease in Systolic blood pressure in one specific group a compared to the others. As most caucasians with Low renin hypertension are older (\>55), presentation with this type of hypertension at a younger age suggests the presence of substantial genetic variation in order to cause the atypical presentation. It is hoped that by identifying the best diuretic for these patients we will also be able to identify: 1. Whether the young low-renin hypertensives can be sub-classified according to their most effective diuretic; 2. Whether this sub-classification helps us to identify the genes and mutations responsible, since these are to expected to be in the so-called sodium channels (i.e. salt pumps)which the kidneys use to prevent salt being excreted in the urine.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Bendroflumethiazide 2.5mg - 5mg | |
| DRUG | Amiloride 20-40mg | |
| DRUG | Spironolactone 50-100mg | |
| DRUG | Frusemide 20-40mg | |
| DRUG | Bendroflumethiazide 1.25-2.5mg/ Amiloride 10-20mg combined |
Timeline
- Start date
- 2006-08-01
- Completion
- 2007-07-01
- First posted
- 2007-02-01
- Last updated
- 2007-02-01
Locations
1 site across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT00429897. Inclusion in this directory is not an endorsement.