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Clinical Study on Bronchoscopic Vaseline Gauze Occlusion Combined with Continuous Negative Pressure Drainage for Treating Bronchopleural Fistula

Clinical Study on Bronchoscopic Vaseline Gauze Occlusion Combined with Continuous Negative Pressure Drainage for Treating Bronchopleural Fistula

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105389
Enrollment
Unknown
Registered
2025-07-02
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

Bronchopleural Fistula (BPF)

Interventions

Experimental Group2:Vaseline Gauze Occlusion Combined with Continuous Negative Pressure Drainage (CNPD)
Control Group:Standard treatment
Experimental Group 2:Vaseline Gauze Occlusion Combined with Conventional Closed Thoracic Drainage Therapy

Sponsors

Emergency General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1?Meets the diagnostic criteria for bronchopleural fistula (BPF).;2?Deemed inoperable by multidisciplinary team (MDT) consultation; 3?Absence of severe n (including shock, severe heorgan dysfunctiopaticrenal insufficiency, upper gastrointestinal bleeding, disseminated intravascular coagulation [DIC], massive hemoptysis, etc.).;4?No coagulation disorders; 5?Tolerance to bronchoscopic interventions and examinations;6.Willingness to participate voluntarily, sign an informed consent form, comply with follow-up procedures, and attend regular follow-up visits at the hospital for at least six months.

Exclusion criteria

Exclusion criteria: 1?Bronchoscopic contraindications: Severe arrhythmia, acute myocardial ischemia, uncontrolled hypertensive crisis, severe organ dysfunction, etc; 2?Ineligible candidates: Patients with concurrent coagulation disorders, severe comorbidities, poor surgical tolerance, or inability to comply. Pregnancy and lactation;3?Pregnant or breastfeeding women.

Design outcomes

Primary

MeasureTime frame
Comparison of Changes in Clinical Cure Rate;

Countries

China

Contacts

Public ContactWang Jingjing

Emergency General Hospital

1096477453@qq.com+86 10 8793 5400

Outcome results

None listed

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