CTRI/2023/01/048951尚未招募未知
Comparative efficacy of Sildenafil and Tadalafil in persons with erectile dysfunction
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Diagnosed with erectile dysfunction as per the ICD-11 criteria.
- •2.Participants willing to provide informed written consent for participation.
- •3.Participants in the age group of 21-50 years
- •4.Participants with adequate literacy to complete the diary card and questionnaires evaluation.
- •5.Participants must be staying with his spouse for a minimum period of six months and anticipate having the same adult female sexual partner during the study.
- •6.Participants must not have received Sildenafil or Tadalafil in the past one month.
排除标准
- •1.Participants taking organic nitrates for any reason.
- •2.Participants having a history of unstable angina,cardiac stents,or life threatening arrythmias.
- •3.Participants with a history of primary hypoactive sexual desire disorder.
- •4.Erectile dysfunction due to spinal cord injury.
- •5.Any clinical history of structural deformity causing erectile dysfunction.
- •6.Participants with a history of undergoing prostate surgery e.g. radical prostatectomy.
- •7.Participants with a clinical history of treated or untreated hypogonadism.
- •8.Participants with below normal serum testosterone levels.
- •9.Participants with a major co-morbid mental illness (i.e. schizophrenia and bipolar
- •10.Participants with a history of hypersensitivity or allergy to Sildenafil or Tadalafil.
研究者
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