Clinical Trials Directory

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UnknownNCT04778605

Modulation of Endothelial Dysfonction Using Vitamin C in Septic Shock Patients

Status
Unknown
Phase
Study type
Observational
Enrollment
30 (estimated)
Sponsor
Assistance Publique - Hôpitaux de Paris · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Compare the microcirculatory reactivity before and after a 30-minute intravenous infusion of 40 mg/kg vitamin C and evaluate intra-individual variation of hemodynamic parameters between T0 and T1.

Detailed description

This is a transversal study allowing to compare the microcirculatory reactivity before and after a 30-minute intravenous infusion of 40 mg/kg vitamin C. Design: • A monocentric, open-label, transversal study Sample size : 30 patients Assessement: Between 6 hours and 24 hours after admission, the patient will be included after collection of the non opposition. There will be two evaluation times: T0 before the start of vitamin C's perfusion, and T1: 1 hour after the end. No interim analysis is planned. Analysis will be performed at the end of the study after data review and freezing of data base.

Conditions

Timeline

Start date
2021-01-26
Primary completion
2021-07-01
Completion
2021-07-01
First posted
2021-03-03
Last updated
2021-03-03

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04778605. Inclusion in this directory is not an endorsement.