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Phase 2, clinical trial to evaluate LifeViroTreat inhalation in mild COVID patient.

Phase 2
Completed
Conditions
Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere
Registration Number
CTRI/2021/07/035233
Lead Sponsor
Supreme Industries
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.RT-PCR positive for nCOVID-19 within last 72 hours

2.Male and female patients with age above 18 years and below 65 years of age.

3.Patient willing to provide informed consent to participate into the trial.

4.Patient able to comply requirement of study and protocol.

5.Patient having SpO2 > 94 %, Respiratory rate < 24/min and temperature < 104 �°F

Exclusion Criteria

1Known hypersensitivity or idiosyncratic reaction to Chlorine or any of related substance or ingredient of the formulation.

2Patient having past history of respiratory disorder like COPD, Asthma etc.

3Patient is on medication before tested nCOVID 19 positive for respiratory disease or disorder (other than viral infection).

4Patients who are diagnosed and/or on treatment for venous thromboembolism, ischemic heart disease, myocardial infarction, congestive cardiac failure, unexplained vaginal bleeding with suspicion of serious underlying condition, history of breast or cervical cancer, malignant tumor

5Patient of Hypertension and/or Diabetes who was not on stable treatment in past 3 month.

6Patient was on immunomodulatory drug

7Have participated in other clinical study related to nCOVID 19

8Patients with other severe acute or chronic conditions that may increase the risk of participation in the study and study treatment, or may interfere with interpretation of study results, and judged by the investigator as not suitable for participation in this clinical trial.

9Known history of Chronic Kidney disease

10Known history of Chronic Liver disease

11Nursing mother or pregnant women

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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