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Efficacy and Safety of Amphotericin B and Azoles in the Treatment of Invasive Fungal Disease

A Retrospective Clinical Study on the Efficacy and Safety of Amphotericin B Compared With Azoles in the Treatment of Invasive Fungal Disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06819410
Enrollment
1000
Registered
2025-02-11
Start date
2021-05-01
Completion date
2025-02-01
Last updated
2025-02-11

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

Conditions

Invasive Fungal Disease

Brief summary

Efficacy and safety of amphotericin B and azoles in the treatment of invasive fungal disease

Detailed description

The medical records, demographic characteristics and clinical data of patients with invasive fungal disease treated with amphotericin B or azoles were collected through the electronic medical record system of Sichuan Provincial People's Hospital from 2021 to 2024. To evaluate the efficacy and safety of these two types of drugs.

Interventions

None listed

Sponsors

Sichuan Provincial People's Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* There is no age limit, gender is not limited * Patients with invasive fungal disease who are treated with polyene antifungals or azole antifungals should be treated for ≥ 7 days.

Exclusion criteria

* Patients with incomplete data or other factors affecting the clinical outcome judgement * Patients who are judged by the investigator to be unsuitable to participate in this study.

Design outcomes

Primary

MeasureTime frameDescription
Clinical success rateThe end of treatment, up to 1 yearClinical success incudes cure or symptom improvement,which means patients are alive, IFD-related symptoms and signs, radiographic abnormalities improve or disappear completely, and microbiological evidence suggests fungal clearance. The proportion of patients with cured or improved symptoms in the total population was analyzed.

Secondary

MeasureTime frameDescription
Safety of amphotericin B and azolesDuring the treatment (1-14 days); the end of treatment (Day 14);Day 28 after the start of treatmentSafety evaluation was mainly based on the incidence of adverse events / adverse reactions in the two groups of patients.

Countries

China

Contacts

Primary Contactlingai Pan, PhD
panlingai2004@163.com17708130236

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026