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临床试验/NCT07574268
NCT07574268已完成4 期

Efficacy of Transcutaneous Electrical Neural Stimulation and Tadalafil in Men With Erectile Dysfunction: A Randomized, Double-Blind, Bi-centric, Placebo- and Sham-Controlled Trial

Menoufia University1 个研究点 分布在 1 个国家目标入组 185 人开始时间: 2025年5月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
185
试验地点
1

研究概览

简要总结

Organic erectile failure is thought to be caused predominantly by neurogenic or vascular disorders. Venoocclusive dysfunction of the corpora cavernosa induces erectile dysfunction in 20-30% and appears clinically by premature erection loss.

The increased venous outflow from the corpora cavernosa can be illustrated as a so called 'venous leakage' by cavernosography being responsible for the therapeutical failure of intracavernously applied vasoactive substances. Cavernous smooth muscle pathology proven in some of the patients with venous leakage gave little hope to reconstructive surgery.

However, own examinations let assume that the etiology of 'venous leakage' is caused by endogenic and exogenic factors. Furthermore, reversible venous leakage was observed. Any therapeutic option of the veno-occlusive dysfunction showed disappointing results with a respective success rate of 20% in the long-term follow-up (surgical venous resection, percutaneous transpenile venous embolisms).

Finally the vacuum device or penile prosthetics are the only therapeutical option for the patients. Physiologically, bulbocavernous and ischiocavernous muscles increase the intracavernous pressure of the tumescent penis.

Regular pelvic floor exercise can be achieved by a physiotherapist which seems to be a time-consuming and expensive procedure, or an advantageous transcutaneous electrical stimulation which is the standard therapy for the treatment of posttraumatic atrophy of the striated muscular system.

Thus an external stimulator device has been developed to evaluate the therapeutical potency of striated muscle exercise in patients with erectile dysfunction. The present clinical study documents the first experiences with this EIS device and outlines its potency for the treatment of erectile dysfunction.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • clinical diagnosis of erectile dysfunction for at least 6 months and confirmed with penile color doppler ultrasound

排除标准

  • Patients with history of cardiovascular disease, contraindication for phosphodiesterase type 5 inhibitor, implanted cardiac pacemakers or defibrillators, anatomically significant penile deformities, active skin lesions at the electrode placement sites or any untreated endocrinal disorder that could affect the erectile function

研究组 & 干预措施

Sham-placebo

Other

This group will receive Sham stimulation along with Placebo similar to tadalafil

干预措施: Sham stimulation (Device)

Active-Placebo

Other

This group will receive active stimulation along with Placebo similar to tadalafil

干预措施: Active TENS (Device)

Sham-Tadalafil

Other

This group will receive Sham stimulation along with tadalafil

干预措施: Tadalafil 5 mg (Drug)

Sham-Tadalafil

Other

This group will receive Sham stimulation along with tadalafil

干预措施: Sham stimulation (Device)

Active-Tadalafil

Other

This group will receive active stimulation along with tadalafil

干预措施: Active TENS (Device)

Sham-placebo

Other

This group will receive Sham stimulation along with Placebo similar to tadalafil

干预措施: Placabo (Drug)

Active-Placebo

Other

This group will receive active stimulation along with Placebo similar to tadalafil

干预措施: Placabo (Drug)

Active-Tadalafil

Other

This group will receive active stimulation along with tadalafil

干预措施: Tadalafil 5 mg (Drug)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ammar Fathi Mohamed AlOrabi

Doctor

Menoufia University

研究点 (1)

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