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Effect of Pratimarsh Nasya, Jalaneti and Rasala in the management of Pratishyaya

A Comparative Study of Pratimarsh Nasya of Anutaila, Jalaneti and Rasala (Classical Shreekhand) in Pratishyaya - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058978
Enrollment
105
Registered
2023-10-20
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Health Condition 1: J00- Acute nasopharyngitis [common cold]

Interventions

None listed

Sponsors

PAB pharmaceuticals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Adults of age group18-75 years irrespective of their caste, race and sex etc. 2. Patients with a diagnosis of Pratishyaya. 3. Patients with signs and symptoms mentioned in the context of vataj, pittaj and Kaphaja Pratishyaya. 4. Patients having written consent.

Exclusion criteria

Exclusion criteria: Patients below age of 18 and more than 75 years. Patients with symptoms of Sannipataj, Raktaj and Dusta Pratishyaya. Patients with nasal malignancy, Raktpitta, glaucoma. Patients not fulfilling the inclusion criteria. Patients having diabetes will not be taken in group C, where Ra

Design outcomes

Primary

MeasureTime frame
Shirahshula (Headache), Gaurav (Heaviness), Ghranaviplav (stuffy nose, loss of sensation of smell), Jwar (Fever), Kash (Cough), Kaphotklesh (mucous nausea), swarbheda (Hoarseness of voice), Aruchi (anorexia), klam (fatique), indriyaanamasamarthyam (inability of sensory organs to perform their normal activities) (Ch.Chi 8/49-50), khsavathu (Sneezing) ch. Chi. 26/105. grading is done for each symptom on 0 to 4 and accordingly stastical tests are performedTimepoint: time points to check are at day 0, 15, 30 and 45

Secondary

MeasureTime frame
Immunoglobulin E (IgE) antibody test, CBC (complete blood count), ESR, Absolute Eosinophil count. Criteria for final assessment of results: Assessment of the clinical study will be done based on the subjective & objective parameters before & after treatment. Observation & results: - The results & observations will be analyzed & presented in accordance with the respective & applicable statistical tests. Timepoint: the tests will be performed at day 0 & day 45

Countries

India

Contacts

Public ContactDr Vishwavasu Gaur

Dr S R Rajasthan Ayurved University Jodhpur Rajasthan India

bkmudgal9@gmail.com09460318138

Outcome results

None listed

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