ManagemEnt of Antifungal Drug in Invasive Aspergillosis:a Real-word Study
Sponsor
Southeast University, China (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06028451
Collaborator
(none)
550
15
Study Details
Study Description
Brief Summary
To assessed the current situation and outcome of critically ill patients with invasive aspergillus infection.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Detailed Description
To assessed the current situation and outcome of critically ill patients with invasive aspergillus infection.
Study Design
Study Type:
Observational [Patient Registry]
Anticipated Enrollment
:
550 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
ManagemEnt of Antifungal Drug in Invasive Aspergillosis:a Real-word Study
Anticipated Study Start Date
:
Sep 15, 2023
Anticipated Primary Completion Date
:
Sep 15, 2024
Anticipated Study Completion Date
:
Dec 15, 2024
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Survivors Critically ill patients with invasive aspergillus infection who survived |
Other: Record the information data
Record the information data
|
Nonsurvivors Critically ill patients with invasive aspergillus infection who not survived |
Other: Record the information data
Record the information data
|
Outcome Measures
Primary Outcome Measures
- mortality [28 day]
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
- Age>18 year-old Diagosed as invasive aspergillus infection
Exclusion Criteria:
- Pregnant
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Southeast University, China
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Jingyuan,Xu,
Principal Investigator,
Southeast University, China
ClinicalTrials.gov Identifier:
NCT06028451
Other Study ID Numbers:
- 2023ZDYYLL01
First Posted:
Sep 8, 2023
Last Update Posted:
Sep 8, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jingyuan,Xu,
Principal Investigator,
Southeast University, China
Additional relevant MeSH terms: