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Exploring the Efficacy and Safety of Bronchoscopic Local Administration of Liposomal Amphotericin B in the Treatment of Invasive Pulmonary Fungal Infections

Exploring the Efficacy and Safety of Bronchoscopic Local Administration of Liposomal Amphotericin B in the Treatment of Invasive Pulmonary Fungal Infections

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122204
Enrollment
Unknown
Registered
2026-04-10
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Refractory invasive pulmonary aspergillosis

Interventions

Conventional Treatment Group:Conventional antifungal therapy
Experimental group:In addition to standard antifungal therapy, administer local intralesional antifungal agent L-AmB through a bronchial catheter guided by bronchoscopy

Sponsors

Shanxi Bethune Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age 18 years or older; 2.Patients with refractory invasive pulmonary aspergillosis and mucormycosis(refer to the expert consensus on the diagnostic pathway of invasive pulmonary fungal disease (2024 Edition);

Exclusion criteria

Exclusion criteria: 1.Expected survival time less than 3 months; 2.History of allergy to amphotericin B; 3.Bleeding tendency or other contraindications to bronchoscopy; 4.Moderate to severe liver disease; 5.Renal insufficiency or failure; 6.Hemodynamic instability; 7.Severe immunodeficiency; 8.Patients of reproductive age who are trying to conceive, pregnant, or breastfeeding; 9.Poor adherence or patients with psychiatric disorders;

Design outcomes

Primary

MeasureTime frame
Imaging Response Rate;

Secondary

MeasureTime frame
Safety Assessment;Clinical response rate;

Countries

China

Contacts

Public ContactLi Xiaochen

Shanxi Bethune Hospital

lixiaochen3n2b@163.com+86 351 2170906

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026