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A Case-control Study on the Clinical Characteristics of 28-day and 90-day Death From Severe Anthrax

A Case-control Study on the Clinical Characteristics of 28-day and 90-day Death From Severe Anthrax

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06365073
Enrollment
80
Registered
2024-04-15
Start date
2024-03-13
Completion date
2024-12-31
Last updated
2024-04-15

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

Conditions

Anthrax

Brief summary

This study is a clinical, multi-center, retrospective, case-control study. Patients clinically diagnosed with severe anthrax who meet the inclusion and exclusion criteria will be included in this study for analysis. Respiratory, circulation, nerve and other vital signs of patients with severe anthrax during hospitalization were recorded, and clinical data such as blood routine, blood biochemistry, coagulation function, myocardial injury, therapeutic drug use, and survival time of patients were recorded, as well as the survival situation of patients 28 days and 90 days after discharge.

Interventions

None listed

Sponsors

Qin Ning
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

1. The typical bacilli with capsules were found in smear examination and culture of various secretions, excretions, blood and cerebrospinal fluid. 2. Multiple organ dysfunction (MODS) in brain, heart, liver, kidney, coagulation or more than one organ failure.

Exclusion criteria

There are other conditions that affect short-term survival.

Design outcomes

Primary

MeasureTime frameDescription
mortality rates of severe anthrax28 days and 90 daysmortality rates of severe anthrax

Secondary

MeasureTime frameDescription
incidence of complicationsin hospitalTo evaluate the incidence of respiratory, circulatory, neurological, digestive, coagulation and other complications of severe anthrax
Peripheral blood biomarkers associated with 28-day and 90-day mortality28 days and 90 daysPeripheral blood biomarkers associated with 28-day and 90-day mortality
the improvement in 28-day and 90-day mortality with treatment for severe anthrax28 days and 90 daysthe improvement in 28-day and 90-day mortality with treatment for severe anthrax

Countries

China

Contacts

Primary ContactQin Ning, professor
qning@vip.sina.com027-83665919

Outcome results

None listed

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