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临床试验/ISRCTN87153230
ISRCTN87153230已完成未知

Subjective effects of a proprietary Eurycoma longifolia and Polygonum minus combination on well-being and sexual performance in patients with mild erectile dysfunction: a randomized controlled trial

Biotropics Malaysia Berhad (Malaysia)0 个研究点目标入组 26 人开始时间: 2012年2月23日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
26

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

性别
Male

入选标准

  • 1. Male subjects between the ages of 40 and 65 at the time of screening, and in a stable heterosexual relationship for at least six months. Both partners had to agree to attempt intercourse at least once a week on average during the study.
  • 2. Subjects with testosterone levels = 450ng/dL
  • 3. Index of erectile dysfunction scores between17-25

排除标准

  • 1. Subjects with a history of prostate cancer, elevated prostate-specific antigen (PSA), benign prostate hypertrophy (BPH) scores = 40, penile anatomical abnormalities, premature ejaculation
  • 2. Cardiovascular disease, resting hypotension (resting systolic blood pressure <90mmHg) or hypertension (resting systolic blood pressure >170mmHg or diastolic pressure >110mmHg)
  • 3. Primary hypoactive sexual desire
  • 4. Seizures
  • 5. Hereditary degenerative retinal disorders or loss of vision
  • 6. Liver disease
  • 7. Clinically significant chronic hematological disease, bleeding disorders
  • 8. Significant active peptic ulceration
  • 9. Symptomatic postural hypotension or syncope within the previous six months
  • 10. Malignancy within the previous five years (other than squamous or basal cell)
  • 11. A positive test for hepatitis B surface antigen or hepatitis C
  • 12. Alcoholism (an alcohol screening score =2)
  • 13. Congenital spinal cord deformities or traumatic injuries, congenital or traumatic brain injuries
  • 13. An abnormal prostate exam during the screening visit

研究者

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