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Effects and Safety of Caspofungin and Corticosteroids in Pneumocystis Pneumonia in Non-HIV Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02603575
Enrollment
60
Registered
2015-11-13
Start date
2015-11-30
Completion date
Unknown
Last updated
2020-03-13

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

Conditions

Pneumocystis Pneumonia

Keywords

Caspofungin, corticosteroids, Pneumocystis Pneumonia, Immunocompromised, Non-HIV, respiratory failure

Brief summary

Pneumocystis Pneumonia is increasing in Immunocompromised Non-HIV Infected Patients. The effects and safety of caspofungin and corticosteroids is not certain in this population. All Immunocompromised Non-HIV patients with respiratory failure were randomized into caspofungin and non-caspofungin group and corticosteroids and non-steroids group. The major outcome is 28 day mortality, the second outcome are time of respiratory rate decreases to less than 25 breath per minute, body temperature lower than 37.3℃.

Interventions

DRUGcaspofungin

70mg ivdrip the first day, then 50mg ivdrip qd

DRUGcorticosteroids

40mg ivdrip q12h for 5 days 40mg ivdrip qd for 5 days 20mg po for 11 days

DRUGSulfanilamides

1.92g q8h

Sponsors

Beijing Chao Yang Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Immunocompromised Non-HIV Infected Patients * Partial arterial O2 pressure(PaO2)/FiO2≤300mmHg * Diagnosed as Pneumocystis Pneumonia

Exclusion criteria

* younger than 16 years old * severe organ failure * allergic to sulfanilamide, caspofungin or corticosteroid

Design outcomes

Primary

MeasureTime frame
mortality28 days

Secondary

MeasureTime frameDescription
Time for release of fever2 daysTime for body temperature less than 37.3℃ for 48 hours
Time for release of respiratory distress2 daysTime for respiratory rate \<25 breathes per minute for 48 hours

Countries

China

Contacts

Primary ContactHangyong He, MM
yonghang2004@sina.com861013693585722

Outcome results

None listed

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