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Effect of Tadalafil Administration on Vasodilatation Mediated by Flow in Patients With Obesity Grade I-II

Acute and Subacute Effect of Tadalafil Administration on Vasodilatation Mediated by Flow in Patients With Obesity Grade I-ii and Erectil Dysfunction

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03905018
Enrollment
80
Registered
2019-04-05
Start date
2019-05-01
Completion date
2019-09-01
Last updated
2019-04-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity and Erectile Dysfuntion

Brief summary

Obesity is a public health problem, not only for its high prevalence, but also because of the comorbidities found in it. Within the physiopathological mechanisms associated with obesity is a low-grade inflammatory state that is associated with endothelial dysfunction Endothelial dysfunction is known to be the beginning of the atherosclerotic process that eventually leads to the development of cardiovascular disease. Erectile dysfunction is an example of endothelial dysfunction, where blood flow is compromised as a consequence of a reduction in the production of nitric oxide among others. Tadalafil, which is an inhibitor of PDE-5, is currently used as a treatment for erectile dysfunction. However, it has been observed that the administration of tadalafil in patients with éndothelial dysfunction decreases arterial stiffness, having a positive effect on it, in addition it reduces the pulse pressure, systolic and diastolic pressure.

Detailed description

: The objective is to evaluate the effect of administration of tadalafil on vasodilatation mediated by flow in patients with obesity grade I-II and erectil dysfunction. A double-blind clinical trial with randomization and control group will be carried out. Male patients aged 25-60 years, BMI ≥30, without comorbidities will be included. They should not be under treatment with iPDE5 or statins, nor should they have uncontrolled ischemic heart disease. To carry out this test, two groups will be created: the first will receive a single dose of tadalafil 20 mg orally and the second will receive 20 mg of calcined magnesia (placebo),after a single administration, 24 hours later the investigators are going to evaluate vasodilatation mediated by. In addition, they will have a metabolic profile at the beginning. For the analysis of results the statistical program SPSS version 21 for Windows will be used. The results will be expressed in averages and standard deviation and normality tests will be applied such as Kolmogorov Smirnof, Shapiro Wilk, as well as the Willcoxon and U Mann Whitney test.

Interventions

tadalafil 20 mg orally ,after a single administration

Sponsors

Centro Universitario de Ciencias de la Salud, Mexico
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Masking description

A double-blind clinical trial with randomization and control group

Intervention model description

A double-blind clinical trial with randomization and control group will be carried out. Male patients aged 25-60 years, BMI ≥30, without comorbidities will be included.

Eligibility

Sex/Gender
MALE
Age
25 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Male patients * Age 25 to 60 years * Obesity grade I-II * .Sign the inform consent form. * Answer the questionary IIFE

Exclusion criteria

. DM 1-2 * Systemic arterial hypertension * Uncontrolled Mixed Dyslipidemia or under Hypolipemiant Treatment with statins. * Active smoking * Precedent of uncontrolled Ischemic cardiopathy. * Use of anti-inflammatory drugs, including Acetylsalicylic acid, antihypertensive, antihyperglucemic, anti-anginal drugs, recent use of antiviral drugs that contains vasoconstrictors. * Hepatic, renal, thyroid, and/or pulmonary decompensated disease. * The precedent of hypersensibility to the phosphodiesterase-5 inhibitors. * Patients that are under treatmen with iPDE

Design outcomes

Primary

MeasureTime frameDescription
vasodilatation mediated by flow24 hoursthe effect of administration of tadalafil on vasodilatation mediated by flow with UNEXEF in patients with obesity grade I-II and erectil dysfunction. A double-blind clinical trial with randomization and control group will be carried out.

Secondary

MeasureTime frameDescription
International Index Erectile Function24 hoursevaluate erectile funtion with a test (IIFE)

Countries

Mexico

Contacts

Primary ContactFernando Grover Páez, PhD
fgroverp@hotmail.com(33) 10585200

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026