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Yi-Qi-Pin-Chuan granules: a Chinese medicine for treatment of acute asthma

Chinese herbs in treatment of acute asthma: a multicentre randomised, double-blind, placebo-controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN61674768
Enrollment
240
Registered
2010-07-29
Start date
2010-07-15
Completion date
Unknown
Last updated
2018-07-30

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

Conditions

Mild to moderate asthma in acute exacerbation Respiratory Asthma

Interventions

Chinese herbs arm: Chinese herbs and beta-2-agonists (salbutamol), systemic steroids (0.5 - 1 mg/kg) if necessary. Placebo arm: placebo and beta-2-agonists (salbutamol), systemic steroids (0.5 - 1 mg

Sponsors

West China Hospital at Sichuan University (China)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Mild to moderate asthma in acute exacerbation 2. Male and female patients between 15 and 75 years 3. Within 72 hours of onset of acute asthma 4. Ability to provide written informed consent

Exclusion criteria

Exclusion criteria: 1. Use of systemic steroids or immunosuppressive agents within one month before recruitment, or history of life-threatening asthma requiring treatment with intubation and mechanical ventilation 2. Maintenance therapy with symbicort, or rescue therapy with formoterol or anticholinergic agents 3. Allergies to any components Yi-Qi-Pin-Chuan granule, as Chinese medicine 4. Current alcoholism or drug abuse 5. Lung diseases other asthma 6. Severe diseases of cardiovascular, hepatic, renal, central nervous system, haematopoietic system cancer 7. Significant medical illness (other than asthma) that is not stable 8. History of respiratory tract infection within the previous 6 weeks 9. Pregnancy or breastfeeding 10. The inability to understand and complete this study 11. Peptic ulcer or gastrointestinal haemorrhage 12. Intolerance to beta-2-agonists or steroids

Design outcomes

Primary

MeasureTime frame
The number of patients with use of systemic steroids and steroid dose, evaluated at days 4 and 8

Secondary

MeasureTime frame
1. The number of patients with hospital admissions, evaluated at days 4 and 8 2. The number of puffs of beta agonists (salbutamol), recorded in asthma diary by the patient 3. Lung functions (PEF), assessed at hours 0, 2, 4, 6, 8, 10, 12 after recruitment, and in morning and evening every day during 7 days of treatment

Countries

China

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 6, 2026