hemoptysis
Conditions
Interventions
experimental group:traditional BAE combined with preoperative CTA
control group:traditional BAE
Sponsors
West China Hospital, Sichuan University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients with massive hemoptysis whose hemoptysis volume per session exceeds 100ml or whose maximum daily hemoptysis volume exceeds 300ml; 2. Patients with minor-medium amount of hemoptysis whose hemoptysis volume is not up to the above standards for large hemoptysis, but whose condition is still repeated within a week after general medical treatment and the patient has the intention of an intervention operation.
Exclusion criteria
Exclusion criteria: 1. Lung malignant tumor highly suspected or confirmed clinically; 2. Lung damage caused by tuberculosis or other causes; 3. emergency intervention for hemostasis is required due to poor efficacy of conservative medical treatment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Early hemoptysis control rate;Dose and duration of patients' radiation exposure;Dose and duration of physician's radiation exposure; | — |
Secondary
| Measure | Time frame |
|---|---|
| Immediate hemostatic success rate;hemoptysis-free time;Long-term hemoptysis control rate;Incidence of hemoptysis during preoperative evaluation;The mortality of hemoptysis during preoperative evaluation;The operation time; | — |
Countries
China
Contacts
Public ContactLuo Fengming
Outcome results
None listed