CTRI/2022/03/041228进行中(未招募)2 期
Phytochemical and Clinical efficacy of Kantaka Panchamoola in the management of Shukra Dushti
Ayurvedic and Unani Tibbia College and Hospital0 个研究点目标入组 64 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 64
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
- •a) Male Patients between the age group of 21-50 years of age.
- •b) Willing and able to participate in the study for 90 days.
- •c) Patients suffering from semen disorders over the past 6 months or more.
- •d) Patients with History of Infertility for the past 3 years.
- •f) Patients with lack of libido / sexual desire/ Impotence/ Erectile Dysfunction.
- •g) Patients with Difficulty in ejaculation of semen.
- •h) Patients ejaculating little quantity of semen after painful coitus.
排除标准
- •a) Men with a total sperm concentration of < 5â??million/mL
- •b) Patients having a history of congenital deformity in genitals.
- •c) Patients with evidence of Malignancy.
- •d) Patients having any type of surgery of genitals.
- •e) Known case of serious hepatic, cardiac or kidney diseases.
- •f) Patients having history of Chronic Fever.
- •g) Patient having any sexual transmitted diseases.
- •h) Patients on prolonged medication with corticosteroids, antidepressants,
- •anticholinergics, immunosuppressant, etc. or any other drugs that may have an
- •influence on the outcome of the study.
- •i) Patients with poorly controlled hypertension (systolic >140 and diastolic >90 mm of
- •Hg) despite of antihypertensive agents.
- •j) Hypersensitivity to any of the trial drugs or their ingredients.
- •k) Patients who have completed participation in any other clinical trial drugs or their
- •ingredients.
研究者
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