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Double Blind Crossover Comparison of Diuretics in the Young
This study is currently recruiting participants.
Verified by University of Cambridge, January 2007
First Received: January 31, 2007   No Changes Posted
Sponsors and Collaborators: University of Cambridge
British Heart Foundation
Information provided by: University of Cambridge
ClinicalTrials.gov Identifier: NCT00429897
  Purpose

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 Intervention
Low-Renin Hypertension
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

MedlinePlus related topics: Dietary Sodium High Blood Pressure
Drug Information available for: Spironolactone Bendroflumethiazide Amiloride
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Crossover Assignment, Efficacy Study
Official Title: Double Blind Crossover Comparison od Diuretics in Young Patients With Low Renin Hypertension

Further study details as provided by University of Cambridge:

Primary Outcome Measures:
  • Difference in systolic blood pressure for subjects' best drug and second best drug.
  • Difference in plasma renin for subjects' best drug and second best drug.

Secondary Outcome Measures:
  • Predictions of best drug

Estimated Enrollment: 30
Study Start Date: August 2006
Estimated Study Completion Date: July 2007
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.
  Eligibility

Ages Eligible for Study:   18 Years to 45 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

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
Please refer to this study by its ClinicalTrials.gov identifier: NCT00429897

Contacts
Contact: Morris J Brown, Professor 01223 336743 mjb14@medschl.cam.ac.uk

Locations
United Kingdom
University of Cambridge - Addenbrookes Hospital Recruiting
Cambridge, United Kingdom, CB2 2QQ
Contact: Morris J Brown, Proffessor     01223 336743     mjb14@medschl.cam.uk    
Sub-Investigator: Sue Hood, RGN - sister            
Sub-Investigator: Diane Picton, RGN- sister            
Sub-Investigator: Tim Burton, Phd, MRCP            
Sponsors and Collaborators
University of Cambridge
British Heart Foundation
Investigators
Principal Investigator: Morris J Brown, Proffessor Cambridge University
  More Information

No publications provided

Study ID Numbers: 1.0
Study First Received: January 31, 2007
Last Updated: January 31, 2007
ClinicalTrials.gov Identifier: NCT00429897     History of Changes
Health Authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency;   United Kingdom: Research Ethics Committee

Keywords provided by University of Cambridge:
Hypertension
Low Renin

Study placed in the following topic categories:
Hormone Antagonists
Diuretics
Sodium Chloride Symporter Inhibitors
Hormones, Hormone Substitutes, and Hormone Antagonists
Vascular Diseases
Amiloride
Bendroflumethiazide
Cardiovascular Agents
Antihypertensive Agents
Furosemide
Hormones
Spironolactone
Aldosterone Antagonists
Hypertension

Additional relevant MeSH terms:
Molecular Mechanisms of Pharmacological Action
Hormone Antagonists
Sodium Chloride Symporter Inhibitors
Physiological Effects of Drugs
Diuretics
Hormones, Hormone Substitutes, and Hormone Antagonists
Vascular Diseases
Amiloride
Bendroflumethiazide
Cardiovascular Agents
Antihypertensive Agents
Pharmacologic Actions
Spironolactone
Membrane Transport Modulators
Aldosterone Antagonists
Natriuretic Agents
Therapeutic Uses
Cardiovascular Diseases
Sodium Channel Blockers
Hypertension

ClinicalTrials.gov processed this record on May 07, 2009