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Effect of Unani Herbal decoction in Asthma

Efficacy of Unani Formulation in Zeequn Nafas (Bronchial Asthma): An Open Labelled Interventional Clinical Trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/03/024011
Enrollment
33
Registered
2020-03-17
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: J454- Moderate persistent asthma

Interventions

Intervention1: Unani Formulation: 12gms in the decoction form orally twice daily before meal for 45days. Intervention2: Unani Formulation: 12gms in the decoction form orally twice daily before meal fo

Sponsors

National Institute of Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient with symptoms of Wheeze, Cough with expectoration, Mild to moderate Paroxysmal Dyspnoea 2.Mild to moderate asthma 3.Patients who have consented for the study

Exclusion criteria

Exclusion criteria: 1.Patients below 18 and above 50 years of age 2.Acute or Severe Exacerbation(FEV1 or PEF 3.Patients with Systemic illnesses such as HTN, IHD, DM 4.Patients with a History of Allergic Rhinitis, COPD, Pneumonia, Occupational lung diseases,Pulmonary tuberculosis 5.Pregnant and lactating women 6.Patients who had received corticosteroids, Bronchodilators or CAM therapy within 2weeks prior to enrolment 7.Patients who have not consented for the study

Design outcomes

Primary

MeasureTime frame
Improvement in FEV1, FEV1/FVC ratio, PEFTimepoint: 0th day and 45th day

Secondary

MeasureTime frame
Improvement in ACT scoreTimepoint: 0th day, 15th day, 30th day and 45th day

Countries

India

Contacts

Public ContactProf Mansoor Ahmad Siddiqui

National Institute of Unani Medicine

mansoorsiddiquidr@gmail.com9448124054

Outcome results

None listed

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