Skip to content

Treatment of difficulty in breathing with Unani medicine Habb-e-Sadr

Clinical validation of a Unani Pharmacopeial formulation Habb-e-Sadr in Zeeq un Nafas(Bronchial Asthma) - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/069434
Enrollment
110
Registered
2024-06-24
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: J459- Other and unspecified asthma

Interventions

Intervention1: Habb-e-Sadar: Two tablets to be taken orally with water twice daily for 6 weeks Control Intervention1: NIL: NIL

Sponsors

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

Eligibility

Inclusion criteria

Inclusion criteria: 1. Males and females of 18-65 years. 2. Patients of Bronchial Asthma for at least 3 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. Patients with Asthma Control Questionnaire Score more than 1.5

Exclusion criteria

Exclusion criteria: 1. FEV1/FVC ratio less than 50%. 2. Pregnant and lactating mother 3. Patient with other Respiratory Tract Infections, tuberculosis and malignancy. 4. Patient of Presence of chronic cough with expectoration for 2-3 months in each of 2 successive years. 5. Patient with co-morbidities, Diabetes Mellitus, Hepatic and Renal Insufficiency. 6. Patients with Tobacco Smoking. 7. Patient with regular use of oral or systemic corticosteroids for conditions other than Asthma.

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 assessed on the basis of Absolute Eosinophil Count (AEC), IgE, Spirometory test, FeNO test and improvement in the Asthma Control Questionnaire (ACQ).Timepoint: At baseline and 2, 4, 6 weeks

Secondary

MeasureTime frame
Haematological & biochemical assessment for safety assessment i.e. CBC, LFT, KFT, Urine Routine & microscopic examination.Timepoint: At baseline and 6 weeks

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

naheedparveen802@gmail.com9213511298

Outcome results

None listed

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