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Treatment of Asthma (difficulty in breathing) by Unani medicine Laooq-e- Zeequn Nafas

Clinical Validation of Unani Pharmacopoeial Formulation Laooq-e- Zeequn Nafas in Zeequn Nafas (Bronchial Asthma)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/02/023639
Enrollment
300
Registered
2020-02-28
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: J452- Mild intermittent asthma

Interventions

Intervention1: Laooq-e-Zeequn Nafas: 5gm twice daily to be taken 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.Males and females of 18-65 years. 2.Patients of Bronchial Asthma for at least 6 months presenting with at least one of the following symptoms: a.Wheeze b.Shortness of breath c.Chest tightness and cough that vary over time and in intensity, d.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 > 1.5.

Exclusion criteria

Exclusion criteria: 1.FEV1/FVC ratio 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
Improvement in signs and symptoms of Zeequn Nafas (Bronchial Asthma)Timepoint: 4 weeks

Secondary

MeasureTime frame
Haematological and biochemical assessment for safety assessmentTimepoint: Investigations will be done at baseline and end of treatment

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