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CTRI Number  CTRI/2021/12/038587 [Registered on: 13/12/2021] Trial Registered Prospectively
Last Modified On: 14/12/2021
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Ayurveda 
Study Design  Randomized, Parallel Group, Placebo Controlled Trial 
Public Title of Study   Antibody response after COVID 19 vaccine provided along with ayurvedic medicine (NOQ19) 
Scientific Title of Study   A prospective, double blind, randomized clinical study to evaluate the antibody response after Covid-19 vaccine when provided along with NOQ19,an ayurvedic medicine 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Anju Dhawan 
Designation  Professor 
Affiliation  AIIMS, New Delhi 
Address  Department of Psychiatry and National Drug Dependence Treatment centre, AIIMS, NEW DELHI

South
DELHI
110029
India 
Phone  01126593236  
Fax    
Email  dranjudhawan@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Anju Dhawan 
Designation  Professor 
Affiliation  AIIMS New Delhi 
Address  Department of Psychiatry and National Drug Dependence Treatment Centre, AIIMS, New Delhi

South
DELHI
110029
India 
Phone  01126593236  
Fax    
Email  dranjudhawan@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Anju Dhawan 
Designation  Professor 
Affiliation  AIIMS New Delhi 
Address  Department of Psychiatry and National Drug Dependence Treatment Centre, AIIMS, New Delhi

South
DELHI
110029
India 
Phone  01126593236  
Fax    
Email  dranjudhawan@gmail.com  
 
Source of Monetary or Material Support  
Sri Sri Institute of Advance Research SSIAR, Bengaluru 
 
Primary Sponsor  
Name  Sri Sri Institute of Advance Research SSIAR 
Address  Bengaluru Karnataka 
Type of Sponsor  Research institution 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Anju Dhawan  AIIMS, Delhi  Raj Kumari Amrit Kaur Out patient department, site for COVID vaccine, AIIMS
South
DELHI 
01126593236

dranjudhawan@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
AIIMS Ethics Committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  normal health persons 
 
Intervention / Comparator Agent  
snoIntervention/ComparatorTypeDrug-TypeProcedure NameDetails
1Intervention ArmDrugOther than Classical(1) Medicine Name: NOQ19, Reference: NA, Route: Oral, Dosage Form: Gutika/Vati/Ghana Vati/Tablets, Dose: 500(mg), Frequency: bd, Bhaishajya Kal: Antarabhakta, Duration: 12 Weeks, anupAna/sahapAna: Yes(details: -WATER), Additional Information: 2 TAB
2Comparator Arm (Non Ayurveda)-PLACEBO PLACEBO (500 mg), 2 tablets, twice a day, for 12 weeks. Placebo made of Starch(100%)
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  Participants yet to receive Covid-19 vaccine
Residence within a 10-kilometre radius of AIIMS hospital
 
 
ExclusionCriteria 
Details  Patients with associated comorbidities like hypertension, type 2 or type 1 diabetes or chronic or acute renal failure or any major systemic illness
Patients on Immuno-suppression therapy
Pregnant Women or lactating mothers

 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant, Investigator and Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
Primary - Change from baseline in count of antibodies following first dose of vaccine, second dose of vaccine


 
4 times, Baseline, after first dose of vaccine, after second vaccine dose,8 weeks after second dose of vaccine


 
 
Secondary Outcome  
Outcome  TimePoints 
Any adverse effects, Refusal rates
 
After first vaccine dose, second vaccine dose, 8 weeks after second vaccine dose 
 
Target Sample Size   Total Sample Size="500"
Sample Size from India="500" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   01/01/2022 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="0"
Months="4"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   Nil 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

coronavirus disease 19 (COVID-19) pandemic is unprecedented and has posed a humongous global challenge to human health and the entire healthcare system. As of 04 May 2021, there have been over 20 million (2 crore) cases of COVID-19 in India and more than 153 million cases globally. During the recent second wave, there has been a continuous rise in COVID-19 cases in various states of India. At present several allopathic drugs are under investigation for treatment of coronavirus disease, but they are failing to contain the spread of virus effectively. No allopathic drug has been proven as a cure so far.

There are many   systems of medicine that are known to increase the immunity and act as immune modulators or to treat the diseases. The Indian ayurveda system of medicine is one of such traditional form of indigenous medical system practiced in India for centuries with considerable success.  Many ayurvedic herbal medicines have beneficial effects, particularly in respiratory disorders.   Most of these herbal medicines constitute a wide variety of alkaloids, flavonoids, phenols, tannins and volatile oils which commonly show anti-viral and anti-bacterial propertiesIn-silico evaluation of a range of herbs has shown strong scientific antiviral and immune enhancing value of ayurvedic herbs. The main protease (Mpro) of SARS-CoV-2 is a key enzyme of coronaviruses and has a pivotal role in mediating viral replication and transcription, making it an attractive drug target for SARS-CoV-2 infection. Thus polyherbal formulations that have been approved for use for any respiratory infections can be re-purposed to prevent and treat COVID patients.  The NOQ19  polyherbal formulation is one such formulation and available in form of a tablet. 

Studies have been conducted to evaluate the mechanism of action of the herbs in NOQ 19 TABLET.    Withanoside V which is present in the plant Ashwagandha(Withania somnifera) is a potent inhibitor of Mpro of SARS-CoV-2, and so proposed as a herbal treatment for COVID-19. Yashtimadhu(Glycyrrhiza glabra) has shown to have potential to bind against spike glycoprotein and non-structural protein-15 of SARS COV-2 in-silico. These proteins are essential for viral infections and replications. So it has been suggested for prevention and management of COVID-19.

The present study has been planned to measure the immune-modulating properties of the Covid-19 vaccine when provided along with NOQ19-by measuring the antibody response .

It is a double blind, randomized controlled trial.  It will have two arms, the experimental group A after COVID vaccine will additionally receive NOQ19 500 mg 1 tablet to be taken twice orally in the morning and evening after food. The control group B will receive COVID vaccine   with a placebo. Both respondents and   investigators will be unaware of the group to which they will be assigned. A total of 500 participants will be recruited following inclusion/exclusion criteria, using a 1:1 allocation ratio, 250 participants will be randomized into each arm. 

Antibody test levels will be measured at baseline, 4 weeks after the first dose, 4 weeks after 2nd dose and 8 weeks after 2nd dose ( 4 times). 


 

 
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