A clinical trial to study the effect of two methods of nasya in patients with chronic sinusitis
- Conditions
- Chronic sinusitis, unspecified, (2) ICD-10 Condition: J329||Chronic sinusitis, unspecified. Ayurveda Condition: DUSHTAPRATISYAYAH,
- Registration Number
- CTRI/2021/06/034121
- Lead Sponsor
- VPSV AYURVEDA COLLEGE KOTTAKKAL
- Brief Summary
This study is a randomised, parallel group trial comparing the effectiveness of alternate day nasya with tulasipatra svarasa and anutaila with alternate day nasya with anutaila in chronic sinusitis for 7 days in a total 42 patients in India. The primary outcome of this study is to assess Rhinisinusitis disability index, Visual analogue scale, Scale of scoring of symptoms for 22 days. Assessment of event evaluation scale and samyak nasya lakshana for 7 days and outcome will be published in the form of dissertation.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 42
1.Eligible for nasya 2.Participants with informed consent.
- 1.Blood stained nasal discharge 2.Nasal polyp 3.
- History of polypectomy and sinus surgery within 3 months 4.
- Other known systemic diseases.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Collected data will be assessed using Rhinosinusitis Disability Index, Visual Analogue Scale and Scale for scoring of symptoms (before trial, after trial and after follow up) for 22 days and Event evaluation scale and Samyak nasya lakṣaṇa (on each day of nasya) for 7 days and outcome will be presented in the form of dissertation. 22 days
- Secondary Outcome Measures
Name Time Method Event evaluation scale and Samyak nasya lakṣaṇa (on each day of nasya) for 7 days 7 days
Trial Locations
- Locations (1)
VPSV AYURVEDA COLLEGE HOSPITAL
🇮🇳Malappuram, KERALA, India
VPSV AYURVEDA COLLEGE HOSPITAL🇮🇳Malappuram, KERALA, IndiaREMYA T MPrincipal investigator9447378935drremyatm@gmail.com