跳至主要内容
临床试验/CTRI/2023/03/050708
CTRI/2023/03/050708尚未招募Unknown

A prospective, two-arm, single blind, single centre, Clinical Study to Evaluate the Safety and Efficacy of NIOX-G Ayurvedic Nasal Spray against Upper Respiratory Tract Viral infections in Vaccinated/ Unvaccinated adult Patients as a curative measures and as a management of Respiratory Allergies & Acute Sinusitis

Khoday Trading Private Limited0 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
Unknown
状态
尚未招募
发起方

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. Subjects who are willing to sign informed consent for participation in the study and willing to adhere to all study procedures.
  • 2. Male or Female subjects aged between 18 to 65 years (both inclusive).
  • 3. Subjects with Upper Respiratory Tract Viral infections/ Respiratory Allergies (Allergic Rhinitis) / Acute Sinusitis.
  • 4. Women of childbearing potential (WOCBP) must be using an acceptable method of contraception to avoid pregnancy throughout the study. WOCBP must have a negative urine pregnancy test at
  • screening visit.

排除标准

  • 1. Subjects with any history of underlying uncontrolled medical illness (such as diabetes, hypertension, liver disease or history of
  • alcoholism, HIV, chronic hepatitis B, hepatitis C Infection or any other serious medical illness).
  • 2. Subjects who are receiving corticosteroids (in a dose equivalent to >= 20 mg prednisone per day), immunosuppressive radiation therapy, or cytotoxic agents.
  • 3. Females who are breastfeeding, pregnant, or attempting to become pregnant.
  • 4. Patients who had undergone nasal surgery within the previous 6 months
  • 5. Patients with nasal polyps, significant deviation of the nasal septum or significant nasal tract structural malformation.
  • 6. Patients with a history of chronic sinusitis, asthma or any other condition that can interfere with the aim of the study.
  • 7. Subjects who have any other condition that, in the opinion of the Investigator, would interfere with a participantâ??s ability to adhere to the protocol (e.g., participants who are mentally or
  • neurologically disabled and who are considered not fit to their participation in the study), interfere with assessment of the
  • investigational product, or compromise the safety of the participant or the quality of the data.

研究者

发起方
Khoday Trading Private Limited

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