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Study on the principle of the treatment of refractory pulmonary tuberculosis cavity with one-way bronchial valve

Study on the principle of the treatment of refractory pulmonary tuberculosis cavity with one-way bronchial valve

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059081
Enrollment
Unknown
Registered
2022-04-24
Start date
2015-03-01
Completion date
Unknown
Last updated
2024-02-11

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

Conditions

tuberculosis

Interventions

Test Group:one-way bronchial valve

Sponsors

The Eighth Medical Center of PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients aged 16-75, with no gender limitation, sputum AFB-positive re-treatment of cavitary tuberculosis, cavity age> 1 year, and drug susceptibility test results show bacterial resistance or multi-drug resistance; (2) Voluntary participation and Sign informed consent; (3) Those who can establish long-term contacts and can assist in completing regular follow-ups.

Exclusion criteria

Exclusion criteria: (1) Age> 75 years; (2) Accompanied by cardiac insufficiency or severe heart disease such as congenital heart disease, coronary heart disease, rheumatic heart disease, pulmonary heart disease, etc., who cannot bear bronchoscopy interventional therapy; (3) Accompanied by severe heart disease Active pneumonia, hemoptysis, tumor, or severe emphysema, bullae, COPD and other lung diseases that affect the effect of valve placement and respiratory function; (4) Congenital or acquired bronchial deformity, deformation, stenosis, etc. Operators performing valve placement; (5) Caseous pneumonia and other dissolving cavities and cavities dominated by lung consolidation are not included in this study; (6) Accompanied by severe liver and kidney damage, unable to withstand systemic chemotherapy (7) Those who are confirmed or suspected to be infected with mold and other pathogens in the cavity; (8) Those who are expected to be effective in the near future after the adjusted plan.

Design outcomes

Primary

MeasureTime frame
Chest CT;Sputum smear for acid-fast bacilli;electronic bronchoscopy;

Countries

China

Contacts

Public ContactHuiru An
jiehebingke_3@163.com13381152893

Outcome results

None listed

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