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Clinical efficacy and safety analysis of pituitrin and ethambutol in the treatment of hemoptysis patients

Clinical efficacy and safety analysis of pituitrin and ethambutol in the treatment of hemoptysis patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104496
Enrollment
Unknown
Registered
2025-06-18
Start date
2025-06-25
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Hemoptysis in bronchiectasis and pulmonary infection

Interventions

Phenolylamide treatment:None
Pituitrin therapy:None

Sponsors

Beijing Friendship Hospital Pinggu Campus,Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.All patients with confirmed bronchiectasis and pneumonia; 2.The patient is in normal mental state, without mental illness or speech dysfunction; 3.Age over 18,under 80 years of age;

Exclusion criteria

Exclusion criteria: 1.Exclusion of patients with drug allergy in this study; 2.Exclusion of patients with coagulation dysfunction and immune dysfunction; 3.Exclusion of lack of complete data; 4.Lactation and pregnancy exclusion;

Design outcomes

Primary

MeasureTime frame
Whether the symptoms of hemoptysis disappear within three days of medication;

Secondary

MeasureTime frame
Coagulation function;Adverse reactions;

Countries

China

Contacts

Public ContactShanliangyu

Beijing Friendship Hospital Pinggu Campus,Capital Medical University

435764168@qq.com+86 15810317843

Outcome results

None listed

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