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Erectile Dysfunction clinical trials

View clinical trials related to Erectile Dysfunction.

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NCT ID: NCT04479917 Completed - Clinical trials for Erectile Dysfunction

Efficacy and Safety of TPN171H in the Patients With Erectile Dysfunction

Start date: July 23, 2020
Phase: Phase 2
Study type: Interventional

This is an exploratory clinical study to presume the optimum usage and dosage for a therapeutic confirmatory study by evaluating the efficacy and safety of TPN171H 5mg, 10mg, 20mg or placebo administered orally in patients with erectile dysfunction. In conclusions, Patients with erectile dysfunction (ED) were administered placebo, TPN171H 5mg, 10mg or 20mg 30 minutes to 4 hours before sexual intercourse for 8 weeks.

NCT ID: NCT04396795 Completed - Clinical trials for Erectile Dysfunction

Safety and Efficacy of Autologous Platelet-Rich Plasma for Erectile Dysfunction.

Start date: May 21, 2020
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate changes in vascular parameters and International Index of Erectile Function (IIEF) scores with the administration of Platelet Rich Plasma (PRP) to participants with Erectile Dysfunction (ED)

NCT ID: NCT04386824 Completed - Clinical trials for Erectile Dysfunction

Erectile Dysfunction in Patients With Non Ocular Behçet's Disease

Start date: June 15, 2019
Phase:
Study type: Observational

It was aimed to demonstrate whether erectile dysfunction is affected by BH pathogenesis and whether there is a relationship between erectile dysfunction and BD pathogenesis by assessing both sexual function and retinal micro-vascular blood flow in BH which may involve vessels from all calibrations and nature.

NCT ID: NCT04383093 Completed - Metabolic Syndrome Clinical Trials

Tadalafil Plus Tamsulosin for Male LUTS and ED

Start date: January 1, 2017
Phase:
Study type: Observational

Metabolic Syndrome (MetS) is a complex epidemic disorder with an impact on both lower urinary tract symptoms (LUTS) and erectile dysfunction (ED). Combination therapy of daily tadalafil and tamsulosin may provide relief to both diseases. Aim of the present study is to assess the impact of combination therapy of Tadalafil 5mg plus Tamsulosin 0.4mg on LUTS and ED, according to presence vs. absence of Mets.

NCT ID: NCT04374994 Completed - Clinical trials for Erectile Dysfunction

Daily Avanafil for Erectile Dysfunction

Start date: September 1, 2018
Phase: Phase 4
Study type: Interventional

In this study, the investigators tried to study the effect of daily avanafil on the serum level of endothelial function markers, as well as its impact on the erectile function in males with erectile and endothelial dysfunction by comparing the results with controls who received placebo.

NCT ID: NCT04363918 Completed - Clinical trials for Erectile Dysfunction

The Use of Bioelectrical Stimulation in the Treatment of Erectile Dysfunction

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

Erectile dysfunction (ED), as defined by the International Consultation on Sexual Medicine, is the consistent and recurrent inability to acquire or sustain an erection of sufficient rigidity and duration to engage in satisfactory sexual intercourse. In the search for other approaches to treat ED the use of bioelectrical stimulation (BES) has been successfully introduced and applied in clinical studies. In the search for other approaches to treat ED the use of bioelectrical stimulation (BES) has been successfully introduced and applied in clinical studies.

NCT ID: NCT04350125 Completed - Clinical trials for Erectile Dysfunction

PRP for the Treatment of Erectile Dysfunction (ED)

Start date: March 4, 2022
Phase: Phase 1
Study type: Interventional

Researchers are trying to determine the safety and efficacy of Platelet Rich Plasma (PRP) in the treatment of Erectile Dysfunction (ED).

NCT ID: NCT04338087 Completed - Clinical trials for Erectile Dysfunction

The Effect of Assisted Reproductive Technology on Male Sexual Function.

Start date: January 1, 2017
Phase:
Study type: Observational

Men participating in assisted reproductive technology treatments will be recruited to a study involving filling erectile function questionnaires throughout fertility treatments, pregnancy and up to 1 year after birth.

NCT ID: NCT04333173 Completed - Clinical trials for Erectile Dysfunction

Endovascular Therapy for Erectile Dysfunction

RE-ACTION
Start date: February 1, 2017
Phase:
Study type: Observational

Brief Summary: Background and pathophysiology Erectile dysfunction is a serious disease with a significant impact on the quality of life. Male erection is a complex mechanism that involves neuro-vascular tissue responses with several phases including arterial dilatation, smooth muscle cells relaxation and ultimately veno-occlusive activation. Vasculogenic erectile dysfunction can be divided in arteriogenic (when there is insufficiency of arterial component of erection due to atherosclerotic plaque encroachment of the penile arteries) or venogenic (where there is insufficiency of the venous component of erection for venous endoleak) Standard treatment Erectile dysfunction is commonly treated by oral phosphodiesterase-5-inhbitor (PDE5i) administration. However, up to 50% of men have a suboptimal response to PDE5-i therapy with the need of additional therapies. New treatment Only recently several studies have been published on percutaneous treatment of ED using POBA, Drug eluting balloons (both paclitaxel and sirolimus, PEB and SES) and drug eluting stents (DES). Aim of the study The study was aimed at evaluating both arteriogenic and venogenic endovascular treatments in patients affected by erectile dysfunction in an Italian patient cohort.

NCT ID: NCT04304742 Completed - Painful Hip Clinical Trials

Radiologist Diagnostic Performance Versus Artificial Intelligence (AI)

RAVIA
Start date: March 1, 2020
Phase:
Study type: Observational

In France, femoral neck fracture is mainly detected with interpretation of pelvis/hip X-ray imaging (French Health Authority recommandation). However, up to 10% of fractures are not identified or misdiagnosed, especially in patients admitted to the emergency department. Indeed, radiologists may be subject to excessive work, wich cause the risk of inaccurate on X-rays diagnosis. The Artificial intelligence (AI) begins study the detection of fratures on medical imaging. In this retropective study, this technology developed by GLEAMER company is tested to evaluate the detection rate of hip fracture and specifically femoral neck fracture, compared to the radiologist diagnostic, in eldery patients admitted in emergency department. AI could optimize the diagnostic performance of radiologists (increase of confidence level) and improve the efficiency of suspected fractures sorting from emergency department.