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Efficacy of Ayush medicine NOQ19 in treatment of COVID-19 patients

Not Applicable
Completed
Conditions
Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere
Registration Number
CTRI/2022/01/039370
Lead Sponsor
Sriveda Sattva Private limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

Hospitalized or in home isolation adult patient aged >18 years

Confirmed COVID-19 infection (RT ââ?¬â??PCR- Upper respiratory tract nasopharyngeal and oropharyngeal swab.

mild and moderate Symptomatic COVID 19 infection with or without comorbidities

Willingness to participate in the study

Indian nationals

Exclusion Criteria

Age less than 18 years

Pregnancy and Lactation

Moribund state in which death is perceived to be imminent (�48 hours)

Patient not willing to participate in the study

Participation in any other clinical study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the effect of NF2 in COVID 19 patients as time to become COV2 RT-PCR negative, duration of hospital stay, time to resolution of symptomsTimepoint: 7 days for each participant
Secondary Outcome Measures
NameTimeMethod
Effect of NF2 therapy on laboratory parameters - CBC, CRP, LFT, KFTTimepoint: Entry and Exit
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