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临床试验/CTRI/2020/05/025332
CTRI/2020/05/025332招募中2 期

Ashwagandha for the Prophylaxis against SARS-CoV-2 Infection: A Randomized Hydroxychloroquine Controlled Clinical Trial in Health Care Providers

MINISTRY OF AYUSH0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中

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.Participants of either sex, 20 to 69 years of age
  • 2.Participants tested negative for COVID-19 by nose and throat swab using RT PCR technique
  • 3.HCQ naïve participants
  • 4.Willing to come for regular follow â?? up visits
  • 5.Written Informed Consent

排除标准

  • 1.Participants with hypersensitivity or Intolerance and contraindications (psoriasis, porphyria and Glucose-6-Phosphate Dehydrogenase deficiency)
  • 2.Pregnant women, lactating women and women of child bearing potential not willing to follow adequate contraception
  • 3.Participants with known allergy or contraindication to Ashwagandha
  • 4Have any Chronic,Severe,Unstable,Uncontrolled medical disease such as Diabetes Hypertension, Cardiac disorders, liver, kidney disorders and lung disorders or other disease of concern which may put the participant at increased risk during the study
  • 5.History of having received any investigational drug in the preceding one month.
  • 6.Prolonged concurrent intake of any drug that is known to prolong QT interval on the ECG as per physician discretion and these drugs include anti-arrhythmic drugs, quinidine, chlorpromazine, haloperidol, olanzapine, thioridazine, fluoxetine, antibiotics belonging to quinolone and macrolide family, antibiotics, fenfluramine and other appetite suppressants, Beta-2 agonists, terfenadine and other anti- histaminic drugs, liquorice and potassium loweringdrugs
  • 7.History of taking any kind of Ayurvedic formulation or any other form of CAM (Complementary Alternative Medicine) therapy in the preceding 2 months
  • 8.Unwilling to come for regular follow-up for the entire duration of the study.
  • 9.Non â?? co-operative attitude of the participant
  • 10.Any condition that, in the opinion of the investigator, does not justify the participantâ??s inclusion in the study.
  • Liver enzymes > 1.5 times of upper normal limits, Serum creatinine > 2 mg/dL, Blood urea > 70 mg/dL

研究者

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