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Prospective, randomized, controlled, multicenter study of thoracoscopic thoracoscopy combined with intrathoracic urokinase injection in the treatment of thoracic infection

Prospective, randomized, controlled, multicenter study of thoracoscopic thoracoscopy combined with intrathoracic urokinase injection in the treatment of thoracic infection

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078352
Enrollment
Unknown
Registered
2023-12-06
Start date
2023-12-06
Completion date
Unknown
Last updated
2023-12-10

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

Conditions

Pleural infection

Interventions

B:Urokinase was injected into the chest
C:Medical thoracoscopy combined with intrathoracic injection of urokinase

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Clinical evidence of infection (as assessed by the competent physician, evidence of infection includes elevated fever, inflammatory markers, such as elevated CRP and white blood cells); Pleural effusion is present at the same time, and the pleural effusion is characterized (with any of these criteria) as gross purulent, positive for bacterial culture, positive for gram staining, or PH < 7.2 (blood gas analysis).

Exclusion criteria

Exclusion criteria: ?. Age < 18 years old; (2) Before receiving fibrinolytic drugs (urokinase, streptokinase, DNase or tPA) treatment; 3. allergic to urokinase; (4) coincidental stroke; ?. Massive bleeding or severe trauma; 6. Unable to tolerate thoracoscopic surgery due to hemodynamic instability or severe hypoxemia; 7. Surgical operation within 5 days, or previously performed ipsilateral thoracic surgery; 8. pregnancy or lactation; ?. Expected survival of less than 3 months, due to diseases other than pleural disease; ? Continuous thoracic drainage was performed before enrollment (without extubation), and no replacement of thoracic drainage tube was required after clinical evaluation.

Design outcomes

Primary

MeasureTime frame
Change rate of pleural shadow;Incidence of adverse reactions (complications);

Secondary

MeasureTime frame
Length of hospitalization;Total hospitalization expenses;

Countries

China

Contacts

Public ContactLi Weimin

West China Hospital of Sichuan University

weimin003@163.com+86 189 8060 1009

Outcome results

None listed

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