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Natriuretic Effect of Telmisartan Versus Placebo in Patients With Mild-to-Moderate Hypertension

7 juillet 2014 mis à jour par: Boehringer Ingelheim

Natriuretic Effect of Telmisartan Versus Placebo in Patients With Mild-to-Moderate Hypertension On a Controlled Sodium Diet (100 mmol/Day)

Study to compare the natriuretic effect of telmisartan to placebo in mild-to-moderate hypertensive patients on a controlled sodium diet as well as to explore the effects of telmisartan on norepinephrine, plasma renin activity (PRA), plasma aldosterone, urine potassium, creatinin, chloride, bicarbonate and uric acid excretion. Additionally it was assessed whether the natriuretic effect disappears after treatment when telmisartan is stopped. The effects of telmisartan on seated clinic blood pressure and the relationship between urine sodium loss and decrease in ambulatory blood pressure after the first dose were assessed descriptively. Assessment of safety was also considered.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Réel)

26

Phase

  • Phase 3

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 65 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Mild-to-moderate hypertension as defined by a morning mean diastolic blood pressure from ≥ 90 and ≤ 115 mmHg and a mean systolic blood pressure ≤ 200 mmHg after five minutes in the seated position at the end of three weeks of placebo run-in treatment
  • Male or female patients between 18 and 65 years of age, inclusive. Patients 60 to 65 years of age must have a screening 24-hour urine creatinine clearance rate of ≥ 1 mL/sec
  • Ability to provide written informed consent

Exclusion Criteria:

  • Pre-menopausal women (last menstruation ≤ one year to start of screening)
  • Post-menopausal women (last menstruation > one year from start of screening or have had a hysterectomy and oophorectomy)

    • Who have < three months of stable estrogen replacement therapy at screening
    • Who will be on progesterone therapy at any time during the trial
  • Known or suspected secondary hypertension
  • Hepatic and/or renal dysfunction as defined by the following laboratory parameters:

    • ALT (alanine aminotransferase) or AST (aspartate aminotransferase) greater than two times the upper limit of reference range
    • Serum creatinine greater than 2.3 mg/dL
  • Bilateral renal artery stenosis; renal artery stenosis in a solitary kidney; post-renal transplant
  • NYHA (New York Heart Association) functional class CHF (chronic heart failure) III-IV
  • Unstable angina, myocardial infarction or cardiac surgery within the preceding three months
  • Stroke within the preceding six months
  • PTCA (percutaneous transluminal coronary angioplasty) within the preceding three months
  • History of angioedema
  • Sustained ventricular tachycardia, atrial fibrillation, or other clinically relevant cardiac arrhythmias as determined by the clinical Investigator
  • Hypertrophic obstructive cardiomyopathy, aortic stenosis, hemodynamically relevant stenosis of aortic or mitral valve
  • Administration of digoxin or other digitalis-type drugs
  • Patients with insulin-dependent and non-insulin-dependent diabetes mellitus
  • History of drug or alcohol dependency
  • Use of antihypertensive agents such as diuretics, ACE inhibitors, angiotensin II antagonists, α-blockers, β-blockers, calcium channel antagonists, direct vasodilators at any time during the trial
  • Administration of other non-antihypertensive medications known to affect blood pressure (e.g., oral corticosteroids, MAO (monoamine oxidase) inhibitors, nitrates) at any time during the trial
  • Chronic administration of high doses of NSAIDS and aspirin (e.g., ibuprofen for rheumatoid arthritis and osteoarthritis in total daily dose in excess of 1600 mg, aspirin in excess of 2 Gm per day)
  • Chronic use of salt substitutes containing potassium chloride; potassium supplements; extreme dietary restrictions
  • Clinically significant sodium depletion as defined by a serum sodium level less than 130 mEq/L
  • Clinically significant hyperkalemia as defined by a serum potassium level greater than 6.0 mEq/L. Clinically significant hypokalemia as defined by a serum potassium level less than 3.0 mEq/L
  • Patients receiving any investigational therapy within one month of signing the informed consent form. Note that patients who have participated in previous telmisartan studies may participate in this study provided there has been at least one month between discontinuing the previous study and signing the consent for the present study
  • Known hypersensitivity to any component of telmisartan
  • Any other clinical condition which, in the opinion of the principal Investigator, would not allow safe completion of the protocol and safe administration of trial medication

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Double

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Telmisartan, low dose
3 weeks placebo run-in (normal diet), 1 week placebo run-in (controlled sodium diet), 2 weeks double-blind treatment ,1 week placebo wash-out (controlled sodium diet)
Expérimental: Telmisartan, high dose
3 weeks placebo run-in (normal diet), 1 week placebo run-in (controlled sodium diet), 2 weeks double-blind treatment, 1 week placebo wash-out (controlled sodium diet)
Comparateur placebo: Placebo
3 weeks placebo run-in (normal diet), 1 week placebo run-in (controlled sodium diet), 2 weeks double-blind treatment, 1 week placebo wash-out (controlled sodium diet)

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
Cumulative urinary sodium loss
Délai: 0-4, 4-8, 8-24 hours post-dose at baseline, day 0, day 7 and 0-24 hours post-dose on days 1-6
0-4, 4-8, 8-24 hours post-dose at baseline, day 0, day 7 and 0-24 hours post-dose on days 1-6

Mesures de résultats secondaires

Mesure des résultats
Délai
Cumulative urine sodium loss
Délai: 0-24 hours post-dose on days 8-13 and 0-4, 4-8, 8-24 hours post-dose on day 14
0-24 hours post-dose on days 8-13 and 0-4, 4-8, 8-24 hours post-dose on day 14
Changes in body weight
Délai: 24 hours post-dose on days -28, -21 to -14, -7, -1, 0, 7, 14 and 22
24 hours post-dose on days -28, -21 to -14, -7, -1, 0, 7, 14 and 22
Changes in plasma norepinephrine
Délai: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Changes in renin activity
Délai: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Changes in aldosterone
Délai: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Changes in urine potassium
Délai: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Changes in creatinine chloride
Délai: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Changes in bicarbonate
Délai: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Changes in uric acid
Délai: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
Cumulative urinary sodium gain during wash-out period
Délai: 0-24 hours post-dose on days from day 15 to 22
0-24 hours post-dose on days from day 15 to 22
Changes in seated clinic blood pressure
Délai: Baseline and day 14
Baseline and day 14
Changes in 24 hour ambulatory Blood Pressure (ABPM) after the first dose of telmisartan
Délai: Day 0
Day 0
Number of patients with adverse events
Délai: up to 50 days
up to 50 days
Number of patients with abnormal findings in physical examination
Délai: Baseline and day 22
Baseline and day 22
Number of patients with abnormal findings in 12-lead electrocardiogram (ECG)
Délai: Baseline and day 22
Baseline and day 22
Number of patients with abnormal changes in laboratory parameters
Délai: Baseline and day 22
Baseline and day 22

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Liens utiles

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 février 1999

Achèvement primaire (Réel)

1 juillet 1999

Dates d'inscription aux études

Première soumission

26 juin 2014

Première soumission répondant aux critères de contrôle qualité

26 juin 2014

Première publication (Estimation)

27 juin 2014

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

8 juillet 2014

Dernière mise à jour soumise répondant aux critères de contrôle qualité

7 juillet 2014

Dernière vérification

1 juillet 2014

Plus d'information

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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