Double Blind Crossover Comparison of Diuretics in the Young

Sponsor
University of Cambridge (Other)
Overall Status
Unknown status
CT.gov ID
NCT00429897
Collaborator
British Heart Foundation (Other)
30
1
11
2.7

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • 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
N/A

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.

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Double
Primary Purpose:
Treatment
Official Title:
Double Blind Crossover Comparison od Diuretics in Young Patients With Low Renin Hypertension
Study Start Date :
Aug 1, 2006
Study Completion Date :
Jul 1, 2007

Outcome Measures

Primary Outcome Measures

  1. Difference in systolic blood pressure for subjects' best drug and second best drug. []

  2. Difference in plasma renin for subjects' best drug and second best drug. []

Secondary Outcome Measures

  1. Predictions of best drug []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Aged 18-45

  • male or female

  • Hypertensive - 3 clinic SBP >=140mmHg; or 3 clinic DBP >=90mmHg; or ABPM or home BP

=130(SBP) or 85(DBP)

  • 24hr Na+<160mmol/l

  • EITHER {Plasma renin<=10mU/L (measured untreated, or whilst receiving only CCB+/-diuretic} + {Plasma renin <=40mU/L (measured on an ACEi or ARB, which approximately double s the plasma renin)} OR Plasma renin <5mU/L (measured untreated, or receiving any antihypertensive drug other than a beta-blocker

Exclusion Criteria:
  • Documented history of gout

  • Abnormal renal function (both elevated serum creatinine and reduced creatinine clearance

  • SBP > 170mmHg or Diastolic >110mmHg despite treatment with permitted background treatment

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Cambridge - Addenbrookes Hospital Cambridge United Kingdom CB2 2QQ

Sponsors and Collaborators

  • University of Cambridge
  • British Heart Foundation

Investigators

  • Principal Investigator: Morris J Brown, Proffessor, Cambridge University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00429897
Other Study ID Numbers:
  • 1.0
First Posted:
Feb 1, 2007
Last Update Posted:
Feb 1, 2007
Last Verified:
Jan 1, 2007
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 1, 2007