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
|
|
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
|
|
Health Condition / Problems Studied
|
Health Type |
Condition |
Healthy Human Volunteers |
normal health persons |
|
Intervention / Comparator Agent
|
sno | Intervention/Comparator | Type | Drug-Type | Procedure Name | Details | 1 | Intervention Arm | Drug | Other 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 | 2 | Comparator 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 properties. In-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).
|