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Clinical Study on Vataja Pratishayaya w.s.r. Allergic Rhinitis and its management with Gojivhadi Avaleha and Chitrak Haritaki Avaleha

Comparative Clinical study on the efficacy of Chitraka Haritaki Avaleha and Gojihwadi Avaleha in the management of Vataja Pratishyaya w.s.r. to Allergic Rhinitis in children - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/071794
Enrollment
100
Registered
2024-08-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J309- Allergic rhinitis, unspecified

Interventions

None listed

Sponsors

All India Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either sex aged between 3-12 years, and known cases of Allergic rhinitis as per the ARIA guidelines, will be included in the study. (ARIA guidelines define allergic rhinitis as the presence of 2 or more recurrent symptoms of recurrent sneezing, watery nasal discharge, nasal congestion, nasal itching, and red itchy eyes, for at least one hour on most of the days or on most days of the season if symptoms are seasonal.) 2. Patients having signs and symptoms of Vataja Pratishyaya will be included in the study.

Exclusion criteria

Exclusion criteria: 1. Patients below 3 yr and above 12 yrs will be excluded. 2. Patients with a history of chronic debilitating diseases like Tuberculosis, Chronic Sinusitis, Nasal polypus, etc., and with other nasal pathology were excluded from the study. 3. Presence of fever, purulent nasal discharge. 4. Children suffering from any cases that require surgical intervention will be excluded.

Design outcomes

Primary

MeasureTime frame
Mean change in the CARAT (Control of Allergic Rhinitis and Asthma Test) Score [Time frame: Form baseline, at the end of 1st week, 2nd week, 3rd week, and at the end of 4th week] Annexure I Timepoint: 4 WEEKS

Secondary

MeasureTime frame
1. Change in subjective and objective signs and symptoms of Vataja Pratishyaya. 2. Mean change in the Laboratory investigations [Time frame: Form baseline and at the end of 4th week] Timepoint: 4 WEEKS

Countries

India

Contacts

Public ContactDr Rahul Dhanraj Ghuse

All India Institute of Ayurveda

ghuserahul@gmail.com9665927690

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026