Trials / Unknown
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.