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Effect of Unani Decoctions in Treating Cough with expectoration

Therapeutic Evaluation of Unani Formulations in the Management of Iltihab al-Shuab Muzmin (Chronic Bronchitis) : A Randomized Single Blind Parallel Group Comparative Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105609
Enrollment
60
Registered
2026-03-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: J410- Simple chronic bronchitis

Interventions

Intervention1: Decoction: The formulation consists of Hyssopus officinalis (Zoofa Khusk) 6 g, Trigonella foenum-graecum (Hulba) 6 g, Glycyrrhiza glabra (Asl-us-Soos) 6 g, Iris ensata (Irsa) 6 g, along

Sponsors

Department of Moalajat Ajmal Khan Tibbiya College Aligarh Muslim University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients in the age group 30-65 years. Patients of either sex. Patient presenting cough with expectoration of at least three months of two consecutive years. Patient with FEV1 greater than or equal to 80 percent predicted (GOLD 1) and FEV1 more than 50 percent and less than 80 percent predicted (GOLD 2) , FEV1/FVC ratio less than 70 percent of predicted value. Prediabetic and diabetics (HbA1c less than 7%) Patient of chronic bronchitis in a stable condition without any signs of acute exacerbation of disease Patient underwent atleast 2 weeks washout period before randomization Those who give written consent

Exclusion criteria

Exclusion criteria: Acute exacerbation of disease Bronchial Asthma Patient demonstrating any radiographic evidence of infiltrates or pulmonary patches on Chest Xray Cor Pulmonale and Congestive Heart Failure, Pregnant & lactating mothers Patient having uncontrolled hypertension (BP greater then or equal to 160 by 100 mm Hg) , CLD, CKD Patient on oxygen therapy Obese Patients (BMI more than 30 kg per m2) Patients who fail to give consent Patients who fail to follow up Mentally retarded persons

Design outcomes

Primary

MeasureTime frame
Statistically significant increase in FEV1 observed from baseline to the end of the studyTimepoint: Day 0 and Day 60

Secondary

MeasureTime frame
Reduction in score of total BCSS and Wheezing scale shows improvement in symptoms. Timepoint: 15th, 30th , 45th, 60th day

Countries

India

Contacts

Public ContactAsra Sadique

Ajmal Khan Tibbiya College

tabassum94tariq@gmail.com8191916786

Outcome results

None listed

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