NCT04870892

Brief Summary

The purpose of this study is to assess the effect of norepinephrine and fluid expansion on capillary refill time during septic shock.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
64

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2021

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 15, 2021

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

April 23, 2021

Completed
11 days until next milestone

First Posted

Study publicly available on registry

May 4, 2021

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2022

Completed
Last Updated

May 4, 2021

Status Verified

April 1, 2021

Enrollment Period

2 years

First QC Date

April 23, 2021

Last Update Submit

April 28, 2021

Conditions

Keywords

septic shockcapillary refill timenorepinephrinefluid infusion

Outcome Measures

Primary Outcomes (1)

  • Difference of capillary refill time before and after the therapeutic change

    Capillary refill time is time required for return of color after application of blanching pressure to a distal capillary bed. In this study, we made a calibrated compression of the skin using a piston for seven seconds, and we recorded CRT with a smartphone's video camera.

    Change from capillary refill time between the 15 min before the therapeutic, Immediately after fluid administration and within the 15 minutes of a change in norepinephrine dose

Secondary Outcomes (3)

  • Correlation between capillary refill time and perfusion index

    Change from capillary refill time between the 15 min before the therapeutic, Immediately after fluid administration and within the 15 minutes of a change in norepinephrine dose

  • Least significant change of capillary refill time

    Change from capillary refill time between the 15 min before the therapeutic, Immediately after fluid administration and within the 15 minutes of a change in norepinephrine dose

  • Difference between capillary refill time on thorax and on the index finger tip

    Change from capillary refill time between the 15 min before the therapeutic, Immediately after fluid administration and within the 15 minutes of a change in norepinephrine dose

Study Arms (2)

Norepinephrine variation

Patients with septic shock, cardiac output monitoring device with the PICCO2 system and decision by the physician in charge to modify the norepinephrine dose.

Fluid infusion

Patients with septic shock, cardiac output monitoring device with the PICCO2 system and decision by the physician in charge to give fluid infusion

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with septic shock, cardiac output monitoring device with the PICCO2 system

You may qualify if:

  • Septic shock
  • Presence of a cardiac output monitoring device with the PICCO2 system (Pulsion Medical Systems, Feldkirchen, Germany)
  • Decision by the physician in charge to perform vascular filling or modification the norepinephrine dose

You may not qualify if:

  • Pregnant
  • Patient under a tutelage measure or placed under judicial protection

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Medical Intensive Care Unit

Le Kremlin-Bicêtre, France

RECRUITING

Related Publications (1)

  • Fage N, Moretto F, Rosalba D, Shi R, Lai C, Teboul JL, Monnet X. Effect on capillary refill time of volume expansion and increase of the norepinephrine dose in patients with septic shock. Crit Care. 2023 Nov 6;27(1):429. doi: 10.1186/s13054-023-04714-0.

MeSH Terms

Conditions

Shock, Septic

Condition Hierarchy (Ancestors)

SepsisInfectionsSystemic Inflammatory Response SyndromeInflammationPathologic ProcessesPathological Conditions, Signs and SymptomsShock

Study Officials

  • Xavier Monnet, MD-PhD

    Service de Médecine Intensive - Réanimation, Hôpital Bicêtre, AP-HP

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Xavier Monnet, MD-PhD

CONTACT

Nicolas Fage, MSC

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Professor

Study Record Dates

First Submitted

April 23, 2021

First Posted

May 4, 2021

Study Start

January 15, 2021

Primary Completion

December 31, 2022

Study Completion

December 31, 2022

Last Updated

May 4, 2021

Record last verified: 2021-04

Locations