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Clinical trial of Guda Vati with tablet Doxophylline in Bronchial Asthma

An open labelled randomized controlled trial to evaluate the efficacy of Guda Vati with tablet Doxophylline in Tamakshwasa with special reference to Bronchial Asthma - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101963
Enrollment
66
Registered
2026-01-23
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: J453- Mild persistent asthma

Interventions

None listed

Sponsors

Dr Rushikesh Vilas Lande
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients having classical signs and symptoms of Tamakashwasa in Avegavastha and symptoms of mild to moderate nature. 2. Patients with known case of Bronchial Asthma having signs and symptoms of mild to moderate nature from more than one year. 3. PEFR more than 300 liters per min 4. Age: 19 to 60 Years. 5. Gender: Irrespective to gender

Exclusion criteria

Exclusion criteria: 1. Pregnant woman Lactating mothers . 2. Cardiac Asthma, Uncontrolled Diabetes Mellitus and Hypertension 3. Patients taking Inhaler daily will be excluded. 4. Patient of Tamakshwasa with secondary infections. Patient suffering from systemic disorders like Tuberculosis, Emphysema, Cor-Pulmonale, etc.

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy of Guda Vati 1gm twice a day when compared with Tablet Doxofylline 200mg in reduction of symptoms of Tamakshwasa over the period of 21 daysTimepoint: base line 0 days, 7 days, 14 days, 21 days

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Rushikesh Vilas Lande

MAMs Sumatibhai Shah Ayurved College Hadapsar Pune

landerushikesh234@gmail.com7039626286

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026