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Treatment of Bronchial Asthma(difficulty in breathing) with Unani medicine Habb-e-Banafsha

Clinical Validation Unani Pharmacopoeial Formulation â?? Habb-e-Banafsha in Zeeq un-Nafas Rewi (Bronchial Asthma)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/05/033781
Enrollment
220
Registered
2021-05-25
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Intervention1: Habb-e-Banafsha: 2 tablets orally thrice daily with lukewarm water for four weeks Control Intervention1: NIL: NIL

Sponsors

Central Council for Research in Unani Medicine CCRUM New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects of either sex between the age group of 18-65 years. 2. Subjects of Bronchial Asthma for at least 6 months presenting with at least one of the following symptoms: Wheeze Shortness of breath Chest tightness and cough that vary over time and in intensity, Expiratory airflow limitation as suggested by a decreased FEV1 3. Objective evidence for reversible airway obstruction (>=12% and >=200 mL change in FEV1 and/or a 25% and 60 L/min change in PEFR) either spontaneously or after treatment. 4. Subjects with Asthma Control Questionnaire Score > 1.5

Exclusion criteria

Exclusion criteria: 1. FEV1/FVC ratio 2. Pregnant and lactating females 3. Subjects with other Respiratory Tract Infections, tuberculosis and malignancy. 4. Subjects of Presence of chronic cough with expectoration for 2-3 months in each of two successive years. 5. Subjects with co-morbidities; Diabetes Mellitus, Hepatic and Renal Insufficiency 6. Subjects with known interstitial lung disease. 7. Subjects with Tobacco Smoking. 8. Subjects with known chronic obstructive pulmonary disease (COPD) 9. Patient with regular use of oral or systemic corticosteroids for conditions other than Asthma. 10. Subjects who are not willing to participate in the study.

Design outcomes

Primary

MeasureTime frame
Improvement in signs and symptoms of Zeeq un-Nafas Rewi (Bronchial Asthma)Timepoint: 1 week

Secondary

MeasureTime frame
Haematological and biochemical assessment for safety assessmentTimepoint: At baseline and after four weeks

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

ccrum507@rediffmail.com9213511298

Outcome results

None listed

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