Fact CheckerSign in

NCT07300293Recruiting

Lactic Acidosis and Prior Metformin Treatment

Prognosis of Lactic Acidosis Upon Admission to Intensive Care According to the Existence of Prior Treatment With Metformin

Source: ClinicalTrials.gov · Last updated 23 Dec 2025

Brief summary (registry, in English)

Metformin is a drug frequently prescribed to patients with type 2 diabetes. Furthermore, diabetes can lead to micro- and macrovascular complications that may cause chronic organ failure. The presence of diabetes also increases the risk of infections. All of these factors contribute to the frequent admission of patients to the ICU who have been receiving metformin treatment in the preceding days. Acute renal failure, which is also frequently observed upon admission to the ICU, increases the risk of metformin overdose. In cases of overdose, metformin acts on several metabolic pathways that can lead to or even accelerate metabolic acidosis, sometimes severe. However, the impact on prognosis is controversial. The role of metformin in lactic acidosis in patients treated for acute illness may be underestimated in routine practice. This study aims to investigate the impact of prior metformin treatment on ICU survival in patients admitted to the ICU with severe lactic acidosis.

Status (registry)
Recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
9 Dec 2025
Start date
6 Nov 2024
Primary completion date
31 May 2026
Lead sponsor
University Hospital, Strasbourg, France
NCT number
NCT07300293

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From 6 Nov 2024 to the primary completion date, 31 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • for whom a limitation of active therapies was implemented before or during the first 24 hours of hospitalization

Other

  • Patient without arterial blood gas measurements during the first 24 hours of admission
  • whose background treatment is unknown and could not be determined

Who the study is looking for

  • Adult patient (≥18 years)
  • Admitted to the intensive care unit of Hautepierre Hospital - Strasbourg University Hospital between January 1, 2014, and December 31, 2023
  • Having experienced lactic acidosis (pH \<7.35 and lactate level ≥5 mmol/L) within the first 24 hours of hospitalization.

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Service de Médecine Intensive - Réanimation - CHU de Strasbourg - France
Coordinator of this site? Confirm its status
StrasbourgFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.