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临床试验/NCT07177326
NCT07177326尚未招募3 期

Combination Therapy of Tadalafil 2.5mg Plus Sildenafil 25mg Versus Tadalafil 5 mg Monotherapy for Treatment of Erectile Dysfunction: A Randomized, Placebo-Controlled Double-Blinded Cross-Over Study

Assiut University0 个研究点目标入组 142 人开始时间: 2025年10月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
尚未招募
入组人数
142
主要终点
Change in Erectile Function (IIEF-5 Score)

研究概览

简要总结

Erectile dysfunction (ED) is characterized by the persistent inability to attain or sustain an erection adequate for satisfactory sexual intercourse. As one of the most common male sexual health disorders, ED exhibits a global prevalence of moderate-to-severe cases ranging between 5% and 20% (1). Although erectile dysfunction is not life-threatening, it can substantially impair both physical and psychosocial well-being, exerting a notable negative impact on the quality of life of affected individuals and their partners.

ED is a multifactorial condition associated with vascular, psychological, and, in some cases, idiopathic causes (2). Management strategies encompass lifestyle modification, pharmacotherapy particularly with phosphodiesterase type 5 (PDE5) inhibitors, vacuum erection devices, intracavernosal injections, and surgical options (1). ED frequently coexists with metabolic and cardiovascular disorders and shows a rising incidence with advancing age and the presence of cardiovascular risk factors (2). Both physiological and psychological mechanisms may underlie the condition; psychological etiologies tend to be more prevalent in younger, otherwise healthy individuals (3). The presence of preserved nocturnal erections is a key clinical indicator suggestive of a psychogenic origin of ED (4).

Phosphodiesterase-5 inhibitors (PDE5Is) represent the primary pharmacologic therapy for ED. Currently, seven PDE5Is (avanafil, lodenafil, mirodenafil, sildenafil, tadalafil, udenafil, and vardenafil) are available in varying dosages and formulations. Their efficacy has been consistently demonstrated in randomized controlled trials (5)(6).

Sildenafil exhibits a rapid onset of action, typically beginning 30 minutes after administration, with an effective duration of 4 to 6 hours and a maximum pharmacological activity lasting up to 12 hours (7). While sildenafil is effective in managing erectile dysfunction, discontinuation rates among responders range from 20% to 50% (8). In contrast, tadalafil, a selective and long-acting PDE5 inhibitor introduced in 2003, has a slightly faster onset around 20 minutes and is recommended to be taken at least 30 minutes before sexual activity. Notably, tadalafil has the longest duration of action among PDE5 inhibitors, with effects lasting up to 72 hours. Approximately 52% of patients are able to achieve successful intercourse within 30 minutes of ingestion (9). The purpose of this study is to evaluate the efficacy and safety of Tadalafil 2.5 mg plus sildenafil 25 mg as a combination therapy versus tadalafil 5 mg monotherapy for 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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • -Men aged 18-70 years with a clinical diagnosis of erectile dysfunction (ED) for ≥3 months.
  • International Index of Erectile Function (IIEF-5) score ≤
  • Stable sexual relationship for ≥3 months.
  • Willingness to adhere to the study protocol and provide informed consent.
  • No prior use of PDE5 inhibitors within 4 weeks before enrollment.

排除标准

  • -Severe cardiovascular disease (uncontrolled hypertension, recent MI/stroke).
  • Hypersensitivity to tadalafil, sildenafil, or any PDE5 inhibitor.
  • Severe hepatic/renal impairment (e.g., CrCl <30 mL/min, Child-Pugh C).
  • Concomitant use of nitrates, strong CYP3A4 inhibitors (e.g., ritonavir, ketoconazole).
  • History of priapism, penile deformities, or radical prostatectomy.
  • Major psychiatric disorders affecting compliance.

研究组 & 干预措施

Group 1

Active Comparator

patients recived Tadalafil 2.5 mg + Sildenafil 25 mg.

干预措施: Tadalafil 2.5 mg (Drug)

Group 1

Active Comparator

patients recived Tadalafil 2.5 mg + Sildenafil 25 mg.

干预措施: Sildenafil 25 mg (Drug)

Group2

Active Comparator

patients recived Tadalafil 5 mg monotherapy

干预措施: Tadalafil 5 mg (Drug)

结局指标

主要结局

Change in Erectile Function (IIEF-5 Score)

时间窗: 12 week

Change in Erectile Function (IIEF-5 Score)

次要结局

未报告次要终点

研究者

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

Mohamed Mostafa Khedr

residant doctor at Assiut university hospital

Assiut University

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