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
  • Other: Record the information data

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

  1. 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:

Study Results

No Results Posted as of Sep 8, 2023