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Treatment of Bronchial Asthma with Unani Medicine Habb-e-Filfil

Clinical validation study to evaluate the safety and efficacy of Unani Pharmacopoeial formulation Habb-e-Filfil in Zeeq-un-Nafas (Bronchial Asthma) - NILL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/092065
Enrollment
210
Registered
2025-07-31
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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-Filfil : 2 tab Twice Daily with water For 4 weeks. Control Intervention1: NIL: NIL

Sponsors

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

Eligibility

Inclusion criteria

Inclusion criteria: 1. Mild and moderate cases of Bronchial Asthma (according to The Global Initiative for Asthma Classification) presenting with at least one of the following symptoms: .Wheeze .Shortness of breath .Chest tightness and cough that vary over time and in intensity. 2.Participants with FEV1 between 60%-80%

Exclusion criteria

Exclusion criteria: 1. Severe case of Bronchial asthma FEV1 BY less than 60% 2. known case of Interstitial lung disease. 3. known cases of chronic obstructive pulmonary disease (COPD). 4. Patient with regular use of oral or systemic corticosteroids for conditions other than Asthma. 5. Participants with other Respiratory Tract Infections, tuberculosis and malignancy. 6. Patients with diseases requiring long term treatment. 7. Patients with Mental disorders affecting drug compliance. 8.Participants with Tobacco Smoking. 9. Pregnant and lactating females.

Design outcomes

Primary

MeasureTime frame
The efficacy of the study drug in the treatment of mild to moderate Zeeq un Nafas (Bronchial Asthma) will be carried out on the basis of Asthma Control Questionnaire (ACQ) and AQLQ (Asthma Quality of Life Questionnaire with standard activities)Timepoint: Weekly

Secondary

MeasureTime frame
Haematological and biochemical investigations for safety assessment i.e., Hemogram, LFT, KFT and Urine Examination: Routine & Microscopic.Timepoint: At baseline and at the end of treatment.i.e., 0 and 4th week

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

javed.ghazal@gmail.com09811810454

Outcome results

None listed

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