NCT07340060

Brief Summary

Statistical Association Between Bicarbonate Levels and Death or Admission to Intensive Care Within 48 Hours in Patients Presenting to the Emergency Department

Trial Health

77
On Track

Trial Health Score

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

Enrollment
6,500

participants targeted

Target at P75+ for all trials

Timeline
3mo left

Started Feb 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress48%
Feb 2026Aug 2026

First Submitted

Initial submission to the registry

January 5, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 14, 2026

Completed
27 days until next milestone

Study Start

First participant enrolled

February 10, 2026

Completed
2 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 12, 2026

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 10, 2026

Expected
Last Updated

March 4, 2026

Status Verified

March 1, 2026

Enrollment Period

2 days

First QC Date

January 5, 2026

Last Update Submit

March 3, 2026

Conditions

Urgency

Outcome Measures

Primary Outcomes (1)

  • Composite criterion: -Admission to a critical care unit within 48 hours of admission to the emergency department. -Death within 48 hours of admission to the emergency department.

    Composite criterion: * Admission to a critical care unit within 48 hours of admission to the emergency department. * Death within 48 hours of admission to the emergency department.

    48 hours

Study Arms (1)

Bicarbonate testing in patients admitted to the emergency department.

Bicarbonate testing in patients admitted to the emergency department.

Eligibility Criteria

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

This research is intended for adult patients admitted to the emergency department at CHD Vendée for whom an ionogram has been prescribed.

You may qualify if:

  • Adult patient
  • Patient with blood ionogram performed upon admission to the emergency department
  • Patient capable of understanding the protocol and not opposed to participating in the research

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Hospitalier Departemental Vendée

La Roche-sur-Yon, France

RECRUITING

Study Officials

  • COLIN Gwenhael

    CHD Vendee

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Clémentin GABORIAU

CONTACT

0251446572clementin.gaboriau@ght85.fr

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 5, 2026

First Posted

January 14, 2026

Study Start

February 10, 2026

Primary Completion

February 12, 2026

Study Completion (Estimated)

August 10, 2026

Last Updated

March 4, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations

FR(1)