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Completed

NCT Number: NCT01743911

Tadalafil Effects in Left Ventricle Diastolic Dysfunction in Resistant Hypertensive Patients

Left ventricle diastolic dysfunction (LVDD) is associated with resistant hypertension. In addition, brain natriuretic peptide (BNP) levels are elevated when LVDD is present. It has been shown that phosphodiesterase-5 (PDE5) inhibition improves left ventricle diastolic function in hypertensive rats, despite any difference in blood pressure levels. Also, left ventricle diastolic function enhancement reduces BNP concentration in hypertensive patients. However, it is unknown if these effects exists in humans with resistant hypertension. Therefore, this study was developed to evaluate if the use of a PDE5 inhibitor (tadalafil) for 2 weeks improves LVDD and its effects in BNP levels in resistant hypertensive patients.

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Key information

Age range

35 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Laboratory of Cardiovascular Pharmacology - FCM - Unicamp

Campinas, São Paulo, 13083-970, Brazil

About this study

Resistant hypertensive patients have a high incidence of left ventricle diastolic dysfunction (LVDD). Lowering blood pressure levels improves diastolic function, however, there is no proved effective treatment specifically for this disease. Studies in hypertensive rats have shown presence of phosphodiesterase-5 in cardiac cells and an improvement in left ventricle diastolic function using a phosphodiesterase-5 (PDE5) inhibitor, the sildenafil. PDE5 has also been demonstrated in human heart cells with cardiac disease. In addition, LVDD is associated with high levels of brain natriuretic peptide (BNP), which reduces with diastolic function improvement. Therefore, it is reasonable to suppose that PDE-5 inhibitor use in humans with LVDD and resistant hypertension could improve diastolic function. Objective: Evaluate the chronic effect of a PDE-5 inhibitor on LVDD and BNP levels in resistant hypertensive patients. Casuistic and methods: 20 resistant hypertensive patients with LVDD types I and II will be evaluated with echocardiography study, ambulatory blood pressure monitoring (ABPM), office blood pressure measurements, endothelial function analysis using the brachial artery flow mediation dilation technique (FMD) and BNP plasma levels. Then, the subjects will receive oral placebo for 2 weeks. After this period, the same exams will be repeated. Two weeks later, the protocol will be performed again to the same 20 patients, using tadalafil (the longest half-life PDE-5 inhibitor) 20mg orally instead of the placebo. Hypothesis: investigators hypothesize that the use of tadalafil will improve left ventricle diastolic function with BNP reduced levels and this effect will be independent of blood pressure decrease or endothelial function improvement.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • resistant hypertension (according to Resistant Hypertension - American Heart Association Statement - 2008);
  • compliance with antihypertensive treatment;
  • age >35 years;
  • left ventricle diastolic dysfunction types I and II

Exclusion criteria

  • valvulopathy
  • decompensated heart failure
  • important cardiac arrhythmias
  • nephropathy
  • hepatopathy
  • autoimmune disease
  • tabagism
  • decompensated diabetes
  • uncontrolled dislipidemia

Treatment and study plan

Sugar Pill

Other

Sugar pills: 20mg orally, once a day for 2 weeks

Other names: No brand name.

Tadalafil

Drug

Tadalafil pills: 20mg orally, once a day for 2 weeks.

Other names: Cialis, Lilly, USA

Primary outcomes

  1. Change in Left Ventricle Diastolic Dysfunction

    Time frame: Baseline and 2 weeks

    Outcome measurement assessed by Echocardiogram before and after a 2-week tadalafil administration period.

Secondary outcomes

  1. Change in endothelial function

    Time frame: baseline and 2 weeks

    Outcome measure assessed by flow-mediated dilation before and after a 2-week tadalafil administration period.

  2. Change in blood pressure levels

    Time frame: Baseline and 2 weeks

    Blood pressure measurements assessed before and after a 2-week tadalafil administration period.

  3. Change in B-type Natriuretic Peptide (BNP-32) levels

    Time frame: Baseline and 2 weeks

    Plasma brain natriuretic peptide (BNP-32)assessed before and after a 2-week tadalafil administration period

  4. Change in cyclic guanosine monophosphate (cGMP) levels

    Time frame: Baseline and 2 weeks

    Cyclic guanosine monophosphate (cGMP) levels assessed before and after a 2-week tadalafil administration period

  5. Change in nitrite levels

    Time frame: Baseline and 2 weeks

    Nitrite levels assessed before and after a 2-week tadalafil administration period.

Sponsors and collaborators

Lead sponsor

University of Campinas, Brazil

Other

Collaborators

  • Fundação de Amparo à Pesquisa do Estado de São Paulo

Registry information

Official study title

Phosphodiesterase-5 Inhibitor (Tadalafil) Two Weeks Administration Period Effects in Left Ventricle Diastolic Dysfunction and BNP Levels in Resistant Hypertensive Patients

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Dec 6, 2012
Registry last updated
Dec 6, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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