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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03140748
Other study ID # PI2016_843_0036
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2018
Est. completion date June 1, 2023

Study information

Verified date September 2023
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Intraabdominal fungal infections with Candida are constantly increasing. Their diagnosis and treatment is difficult. Morbidity and mortality are high. Β-D-Glucan has been proposed as a marker of systemic fungal infection in candidemia. Moreover, its kinetics is associated with therapeutic success. On the other hand, there are no data on intraabdominal infections that are much more frequent. The objective of the study is to evaluate the initial levels of β-D-glucan and its daily kinetics during the treatment of fungal peritonitis in resuscitation compared to a control group with a yeast-free peritonitis.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date June 1, 2023
Est. primary completion date August 22, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Major Patient (age = 18 years) - Community or associated peritonitis, operated and hospitalized in resuscitation - Affiliation to a social security scheme Exclusion Criteria: - Allergy known to echinocandins - Dying Patient - Limitation of care - Predictable duration of follow-up = 10 days - Transfusion within 3 months - Patient minor, patient under guardianship or curatorship

Study Design


Intervention

Other:
To evaluate the initial levels and kinetics of serum ß-D-glucan
To evaluate the initial levels and kinetics of serum ß-D-glucan during fungal peritonitis compared to a control group of yeast-free peritonitis

Locations

Country Name City State
France CHU Amiens Picardie Amiens Picardie

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood determination of serum ß-D-glucan kinetics in patients with peritonitis Blood determination of serum ß-D-glucan kinetics in patients with peritonitis 28 days
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