Plain English Summary
Background and study aims
Allergic rhinitis is an immune response of the nasal mucosa (lining of the nasal cavities) to airborne allergens and involves nasal congestion, watery nasal discharge, itching of the nose and sneezing. Allergic rhinitis is commonly defined as seasonal or perennial, depending upon whether symptoms occur at defined yearly intervals or throughout the year, respectively. Allergic rhinitis is not life threatening, but it is an annoying and disturbing disease for the patient due to its chronicity and aggravation when exposed to allergic agents. Furthermore allergic rhinitis is a considerable cause of widespread morbidity, medical treatment costs, reduced work productivity and lost school days. The symptoms of allergic rhinitis may significantly affect a patient’s quality of life and can be associated with conditions such as fatigue, headache, cognitive impairment and sleep disturbances. Appropriate management of allergic rhinitis is an important component in the effective management of coexisting or complicated respiratory conditions such as asthma, sinusitis and sleep apnea. In this context, various complementary and alternative medicine treatments have been used for this condition in clinical practice. The Ayurveda system of medicine is the most common complementary medicine system in Sri Lanka. The aim of this study is to find out whether the use of two preparations (decoction and its freeze dried powder) over a period of 4 weeks is able to cure the symptoms of allergic rhinitis.
Who can participate?
Male and female patients aged 18 to 65 with allergic rhinitis
What does the study involve?
Participants are randomly allocated to receive either one of two Ayurveda treatments (traditional herbal decoction or a sachet containing freeze dried ingredients of herbal decoction) or the antihistamine loratidine for 4 weeks. Nasal symptoms are assessed at the start of the study, after four weeks of treatment, and after one month and two months of follow up.
What were the possible benefits and risks of participating?
The participants receive information and advice from a specialized medical team. In addition their participation may help to develop an Ayurveda drug treatment for allergic rhinitis.
Where is the study run from?
National Ayurveda Teaching Hospital (Sri Lanka)
When is the study starting and how long is it expected to run for?
January 2019 to May 2021
Who is funding the study?
University Grants Commission (Sri Lanka)
Who is the main contact?
Dr Jeevani Dahanayake
jeevanimd@iim.cmb.ac.lk
Trial website
Contact information
Type
Scientific
Primary contact
Dr Jeevani Dahanayake
ORCID ID
http://orcid.org/0000-0002-9085-918X
Contact details
Institute of Indigenous Medicine
University of Colombo
Sri Lanka
Colombo
0094
Sri Lanka
+94 (0)772961461
jeevanimd@iim.cmb.ac.lk
Type
Public
Additional contact
Dr Pathirage Kamal Perera
ORCID ID
http://orcid.org/0000-0003-0337-1336
Contact details
Institute of Indigenous Medicine
University of Colombo
Colombo
0094
Sri Lanka
+94 (0)716419072
kamalperera@iim.cmb.ac.lk
Type
Scientific
Additional contact
Prof Priyadarshani Galappatty
ORCID ID
http://orcid.org/0000-0002-9279-9053
Contact details
Department of Pharmacology
Faculty of Medicine
University of Colombo
Colombo
0094
Sri Lanka
+94 (0)718655651
p.galappatthy@pharm.cmb.ac.lk
Additional identifiers
EudraCT number
Nil known
ClinicalTrials.gov number
Nil known
Protocol/serial number
2016/Mphil-PhD/029
Study information
Scientific title
Development of an Ayurvedic pharmaceutical preparation for allergic rhinitis and evaluation of its safety and efficacy
Acronym
AyudrugAR
Study hypothesis
Freeze dried powder of Tamalakyadi decoction will have similar efficacy and safety in treating patients with allergic rhinitis compared to the traditional decoction and antihistamines.
Ethics approval
Approved 22/01/2019, Ethics Review Committee (Institute of Indigenous Medicine, University of Colombo, Rajagiriya, Sri Lanka; Tel: +94 (0)112692395; Email: ethicsreviewiim@gmail.com), ref: ERC 18/76
Study design
Three-arm open-label non-inferiority randomized control clinical trial
Primary study design
Interventional
Secondary study design
Randomised controlled trial
Trial setting
Hospitals
Trial type
Treatment
Patient information sheet
Not available in wed format, please use contact details to request a participant information sheet.
Condition
Allergic rhinitis
Intervention
This will be a three-arm open-label non-inferiority randomized control trial in patients with allergic rhinitis. Consecutive consenting sample method will be followed to select participants of the arms for the study. A blocked design will be used, using an online statistical computing web programming to generate the randomization schedule (research randomizer https://www.randomizer.org). Eligible subjects will be randomly assigned to Arm I, Arm II and Arm III to receive herbal decoction, freeze-dried powder of herbal decoction and antihistamine for 28 days.
The patients of Arm I will be treated with herbal decoction (Tamalakyadi decoction), 120 ml twice a day after meals. Arm II patients will be treated with 6 g of freeze-dried powder of herbal decoction. The powder should be dissolved in 240 ml of hot water and should take 120 ml twice a day after meals. The patients of Arm III will receive antihistamine (loratidine 10 mg) at night taken with 240 ml of water. Patients belong to three arms have to visit the clinic weekly.
Total Nasal Symptom Score (TNSS) and IgE level of patients will be the primary efficacy endpoints. The mean difference in TNSS and IgE level will be compared between the three arms as the primary endpoints at the end of 28 days. The TNSS will be again analyzed after 1 month and 2 months of treatment at follow-up visits.
Mean score of daytime nasal symptoms, nighttime nasal symptom, non-nasal symptoms and Health-Related Quality of Life score will be used as secondary endpoints in the clinical trial. These symptom scores will be analyzed by using the information mentioned in rhinitis diary card of the patient. This diary cards will be collected weekly at the clinic.
Follow up – patients will be assessed after 1 month and 2 months at the clinic without a drug intervention.
Intervention type
Drug
Phase
Phase II
Drug names
Herbal decoction of Tamalakyadi decoction, freeze-dried powder of Tamalakyadi decoction, antihistamine (loratidine)
Primary outcome measure
1. Nasal symptoms (watery rhinorrhea, sneezing, nasal obstruction, nasal itching) measured using the Total Nasal Symptom Score (TNSS) of allergic rhinitis patients at baseline and the end of intervention (after four weeks, after one month of follow up and two months of follow up)
2. Serum Immunoglobulin E level measured using chemiluminesent enzyme immunoassay (EIA) at baseline and after intervention
Secondary outcome measures
1. Mean score of daytime nasal symptom score
2. Mean score of nighttime nasal symptom score
3. Mean score of non-nasal symptoms
Patient self-rated symptom scores (daily rhinitis diary card) and allergic rhinitis grading symptoms collected on a weekly basis during the assessment period. The measurement of symptoms on a 4-point rating scale with the following definition will be used:
• 0 = absent symptoms (no sign/symptom evident)
• 1 = mild symptoms (sign/symptom clearly present, but minimal awareness; easily tolerated)
• 2 = moderate symptoms (definite awareness of sign/symptom that is bothersome but tolerable)
• 3 = severe symptoms (sign/symptom that is hard to tolerate; causes interference with activities of daily living and/or sleeping)
4. Health-related quality of life measured using HRQoL questionnaire (Valero et al, 2009 & 2013) at baseline and end of intervention (after four weeks, one month of follow up and two months of follow up)
Overall trial start date
22/01/2019
Overall trial end date
01/05/2021
Reason abandoned (if study stopped)
Eligibility
Participant inclusion criteria
1. Age 18-65 years at the time of enrollment, of either sex
2. No known systemic disorders
3. Newly diagnosed allergic rhinitis patients on Ayurvedic treatment
4. No history of drug allergy
5. Non-pregnant and non-breastfeeding
6. Have given written informed consent to participate in this study
7. Total Nasal Symptom Score (TNSS) more than 6
Participant type
Patient
Age group
Adult
Gender
Both
Target number of participants
70 patients for each arm
Participant exclusion criteria
1. Patients with deviated nasal septum/nasal polyps/nasal growth/adenoids/asthma
2. Patients with impaired liver and kidney functions, anaemia, and unstable cardiovascular conditions or cerebrovascular conditions
3. Currently or previously treated for any malignancy
4. Patients on steroid therapy
5. Already on treatment with herbal decoction or antihistamines
6. Pregnant or lactating mothers
7. Illiterate patients without a literate relative/guardian who can explain the procedures and maintain the patient diary
Recruitment start date
30/05/2019
Recruitment end date
30/05/2021
Locations
Countries of recruitment
Sri Lanka
Trial participating centre
National Ayurveda Teaching Hospital
Dr. N. M. Perera Mawatha, Borella, Colombo 8
Colombo
0094
Sri Lanka
Sponsor information
Organisation
University of Colombo
Sponsor details
Faculty of Graduate Studies 35/30
Prof Stanley Wijesundera Mawatha
Colombo 7
Colombo
0094
Sri Lanka
+94 (0)11 205 56 56
office@fgs.cmb.ac.lk
Sponsor type
University/education
Website
Funders
Funder type
Government
Funder name
University Grants Commission - Sri Lanka
Alternative name(s)
UGC
Funding Body Type
government organisation
Funding Body Subtype
National government
Location
Sri Lanka
Results and Publications
Publication and dissemination plan
Planned publication in high impact peer-reviewed journals.
Additional documents will be available upon request from Dr Jeevani Dahanayake (jeevanimd@iim.cmb.ac.lk). Study protocol planned to published in a peer-reviewed indexed journal.
IPD sharing statement
The datasets generated during and/or analysed during the current study are/will be available upon request from Dr Jeevani Dahanayake (jeevanimd@iim.cmb.ac.lk). Study participant data sheets will not include contact or identifying details. Study data entry and study management systems used by clinical sites will be secured and password protected. At the end of the study, all study databases will be de-identified and archived. Availability of raw data of the study is based on the above conditions.
Intention to publish date
01/05/2021
Participant level data
Available on request
Basic results (scientific)
Publication list
2020 protocol in https://pubmed.ncbi.nlm.nih.gov/31910896/ (added 04/08/2020)