EFFECT OF PRADHAMANA NASYA AND NARADIYA LAXMIVILAS RASA FOR THE MANAGEMENT OF PATIENTS SUFFERING FROM KAPHAJA PRATISYAYA

Clincal trial to evaluate efficacy & safety of Pradhamana Nasya as an add on treatment to NARADIYA Laxmivilas Rasa for the management of Kaphaja Pratisyaya vis-a-vis Rhinitis

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/02/040162

Enrollment

Registered

2022-02-10

Start date

Unknown

Completion date

Unknown

Last updated

2022-02-21

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

Eligibility

Inclusion criteria

Inclusion criteria: Age:18-50yrs 1 Both male and female 2 Patients having sign and symptoms of Kaphaja Pratishyaya as per Ayurveda classics. 3 Patient giving their consent and able to participate in the study for 8 weeks. 4 Patient fit for Pradhamana Nasya

Exclusion criteria

Exclusion criteria: -Sannipataja Pratishyaya (Pinasa) characterised by loss of smell (anosmia) • Raktaja Pratishyaya (Epistaxis), . Patient unfit for Pradhamana Nasya -Tuberculosis - Chronic Bronchitis (cough > 3years) - Bronchial Asthma - Lupus in the nose. • Pregnant ladies and lactating mother

Design outcomes

Primary

Measure	Time frame
Change in sign and symptoms of Kaphaja Pratishyaya. changes in Rhinitis Control Assessment Test.Timepoint: 8th, 15th & 23rd days during treatment	—

Secondary

Measure	Time frame
-Rhinitis Control Assessment Test - SF-36 questionnaires/ rhino-conjunctivitis quality of life questionnaire (RQLQ). - Change in IgE and AECTimepoint: 8th, 15th & 23rd days during treatment and Follow up - 30 days	—

Countries

India

Contacts

Public ContactDr Dimple Meena

ALL INDIA INSTITUTE OF AYURVEDA

divyakajaria@gmail.com8826167515

Outcome results