Ayurvedic treatment for allergic rhinitis using Ayurvedic medicine. The treatment consists of taking Haridrakhanda orally and using Anu Taila Nasya (an oil) with and without Saraladi Dhoomapana (a type of steam inhalation).
- Conditions
- Allergic rhinitis, unspecified. Ayurveda Condition: VATAJAPRATISYAYAH,
- Registration Number
- CTRI/2023/04/051273
- Lead Sponsor
- I.T.R.A.,Jamnagar
- Brief Summary
**Introduction**:Many research works have been carried out on Vataja Pratishyaya (Allergic Rhinitis) in Ayurveda and also in contemporary system of medicine, Vataja Pratishyaya (Allergic Rhinitis) still remains as a hazardous problem as it has more chances of recurrent episodes and serious complications. Haridrakhanda has Rasayana and Rogahara property. It may give an immune modulator effect which will be effective in the management of Vataja Pratishyaya (Allergic Rhinitis). Nasya with Anu Taila will have a great effect on symptoms of Pratishyaya, as Nasa is considered as direct gateway to the Shirah. Dhoomapana is one of the best therapies for diseases of Supra clavicular region specially Vata Kapha predominancy. So, the study has been planned to find out the management from the ancient texts which is effective and cheap. **Information on the Trial procedure and Drug:** Here in Group A, we are giving 6gm of Haridrakhanda twice a day with lukewarm water before meal, 6 drops of Anu Taila Nasya in each nostril in morning (3 sittings of Nasya for 7 days with interval of 3 days) followed by Saraladi Dhoomapana 9 puffs in each nostril. In Group B, 6gm of Haridrakhanda twice a day with lukewarm water before meal and 6 drops of Anu Taila Nasya in each nostril in morning (3 sittings of Nasya for 7 days each with interval of 3 days). We assure that we will prepare formulations with as per S.O.P in the Pharmacy of I.T.R.A. **Description of the Process:** In present study, participants who will be clinically diagnosed and confirmed cases of Vataja Pratishyaya (Allergic Rhinitis) enlisted in inclusion criteria will be enrolled, minimum 30 patients and will be divided in to 2 groups by computer generated randomization technique, having minimum 15 patients in one group. In Group A, they will be given 6gm of Haridrakhanda twice a day with lukewarm water before meal, 6 drops of Anu Taila Nasya in each nostril in morning (3 sittings of Nasya for 7 days with interval of 3 days) followed by Saraladi Dhoomapana 9 puffs in each nostril. In Group B, 6gm of Haridrakhanda twice a day with lukewarm water before meal and 6 drops of Anu Taila Nasya in each nostril in morning (3 sittings of Nasya for 7 days each with interval of 3 days) **Follow-up:** Follow up will be for one month duration at interval of 15 days. **Side Effects:** We will follow closely and keep track of any unwanted effects. We may use some other medicines or stop the usage of drug to decrease the symptoms of the side effects. **Results:** The efficacy of the therapy will be assessed on the basis of subjective criteria. Benefits: Project will help us to resolve the research question. There may not be any benefit for the society at this stage of the research, but future generations are likely to be benefited as to find out proper treatment protocol for the management of Rhinitis. Collected information from this research project will be kept confidential, all outcomes will be noted in tabular form and appropriate statistical tests will be applied to compare the effect.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 30
- 1.Patient between age group of 18 and 50 years.
- 2.The diagnosis of the disease shall be done with signs and symptoms of Vataja Pratishyaya (Allergic Rhinitis) i.e., Gala-Talu-Austha Shosha (Dryness), Svaropaghata (Hoarsness of voice), Kshavthu (Sneezing), Nasa Srava (Nasal discharge), Nasaavrodha (Nasal obstruction).
- 1.Patient below 18 and above 50 years.
- 2.Cases which require surgical intervention like Nasal polyps would be excluded.
- 3.Patients suffering from any chronic debilitating disease like Tuberculosis, Diabetes Mellitus, Asthma and other respiratory or nasal problems.
- •Pregnant ladies and lactating mothers.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) ANTERIOR RHINOSCOPIC EXAMINATION 30 DAYS. | WILL BE ASSESED ON 0 DAY (BEFORE) AND 31ST DAY (AFTER) THE TREATMENT. 2) NASAL ENDOSCOPY 30 DAYS. | WILL BE ASSESED ON 0 DAY (BEFORE) AND 31ST DAY (AFTER) THE TREATMENT.
- Secondary Outcome Measures
Name Time Method 1) KSHAVATHU (SNEEZING) 2) NASA SRAVA (NASAL DISCHARGE)
Trial Locations
- Locations (1)
Institute of Teaching and Research in Ayurveda
🇮🇳Jamnagar, GUJARAT, India
Institute of Teaching and Research in Ayurveda🇮🇳Jamnagar, GUJARAT, IndiaNisha M VachhaniPrincipal investigator9998725805nishavachhani548@gmail.com