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The auxiliary Effect of Lianhuaqingwen (LHQW) in Acute Exacerbation of Chronic Obstructive Pulmonary Disease (AECOPD): A randomized, controlled clinical trial

The auxiliary Effect of Lianhuaqingwen (LHQW) on The Airway Inflammation in Acute Exacerbation of Chronic Obstructive Pulmonary Disease (AECOPD)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003240
Enrollment
Unknown
Registered
2013-04-09
Start date
2013-01-01
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

Chronic Obstructive Pulmonary Disease

Interventions

Lianhuaqingwen therapy group:based treatments+Lianhuaqingwen capsules
conventional therapy group:based treatments+ placebo

Sponsors

Huashan hospital, Fudan university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
85 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Aged 50 to 85 years old, gender not limited; 2. COPD was defined according to recent guidelines(GOLD); 3. Deteriorated beyond everyday situationand the need to change the drug treatment; 4. All volunteers signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. With respiratory failure (quiet breathing, the sea level, no oxygen, PaO2 50 mmHg), and have to use mechanical ventilation; 2. Combined serious primary diseases and immunocompromised disorders such as cardiovascular diseases, tumor and autoimmune diseases et al.; psychiatric patients; Pregnancy or breast-feeding women; With severe stomach disease, can't tolerate oral drug therapy; 3. Upper or lower respiratory tract infection in two months before the study; 4. Use traditional Chinese medicine treatment of 36 hours; 5. Have allergy history of medicine composition; 6. Participated in other clinical subjects within three months.

Design outcomes

Primary

MeasureTime frame
COPD assessment test scale;Chinese Medicine Symptom Complex Score scale;GOLD grade;

Secondary

MeasureTime frame
interleutin-8;tumor necrosis factor alpha;interleukin-17;interleukin-23;

Countries

China

Contacts

Public ContactCHEN Xiao-dong
xdchen8@hotmail.com+86 021 52888480

Outcome results

None listed

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