跳至主要内容
临床试验/CTRI/2022/03/041228
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

发起方
Ayurvedic and Unani Tibbia College and Hospital

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