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Xiaoqinglong Granules for the treatment of mild and persistent asthma with: a randomized controlled, double-blind clinical study

Study on the construction of the whole effect assessment index system over asthma with TCM and its assessment method

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10001072
Enrollment
Unknown
Registered
2010-11-09
Start date
2010-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

mild/persistent asthma

Interventions

A:Seretide + Xiaoqinglong granules
B:Seretide + Placebo

Sponsors

China National Center for Biotechnology Development
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. 2nd or 3rd grade bronchial asthma; 2. 18-65 years; 3. TCM cold pattern criteria; 4. signed informed consent; 5. not use hormones, theophylline or beta 2 agonists in 2 weeks.

Exclusion criteria

Exclusion criteria: 1. severe persistent or intermittent attacks bronchial asthma patients; 2. less than 18 years old or over 65 years; 3.history of serious diseases, or laboratory data suggest that people with severe systemic disease ( such as liver and kidney insufficiency), mental disorder; 4.pregnant women, nursing women, allergic; 5. allergied with drugs known or experimental drugs in certain herbs; 6. has participated in other clinical trials in 4 weeks; 7. seasonal asthma, the length of treatment less than 2 months each year; 8. patients diagnosed as heat Asthma.

Design outcomes

Primary

MeasureTime frame
asthma control;

Secondary

MeasureTime frame
asthma QOL questionaire of Juniper;integral of symptom;Asthma control test Score;

Countries

China

Contacts

Public ContactQinglin Zha
zhaqinglin@gmail.com+86 13330062517

Outcome results

None listed

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