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Clinic study of safflower yellow on the treatment in acute exacerbation of chronic obstructive pulmonary disease

Clinic study of safflower yellow on the treatment in acute exacerbation of chronic obstructive pulmonary disease

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17014176
Enrollment
Unknown
Registered
2017-12-27
Start date
2013-02-18
Completion date
Unknown
Last updated
2018-01-08

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

Controll Group:conventional therapy

Sponsors

The people's Hospital of Pujiang County, Sichuan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Signed informed consent; 2. According to the diagnostic standard of Chinese society of respiratory diseases committee guidelines defined[2011]; 3. aged 40 to 85 years.

Exclusion criteria

Exclusion criteria: 1. bronchial asthma; 2. bronchiectasis; 3. Pulmonary tuberculosis fibrosis; 4. pulmonary cystic fibrosis; 5. Women in pregnancy or lactation; 6. Coagulation disorders, bleeding tendency; 7. Patient is allergic to safflower yellow; 8. Patient is currently in other medical research; 9. The patients with serious diseases of liver and kidney, hematopoietic system endocrine system; 10. the mentally ill.

Design outcomes

Primary

MeasureTime frame
Days of Mechanical ventilation;The 28 day mortality;The curve of 28 day survival rate;

Secondary

MeasureTime frame
Average Length of Stay, ALOS;

Countries

China

Contacts

Public ContactLi Xiaojin

The people's Hospital of Pujiang County, Sichuan

939590330@qq.com+86 18980808557

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 22, 2026