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Fluid Administration in Ketoacidosis (DRINK)

Diabetic Keto-acidosis

LO ESENCIAL

De qué trata este estudio

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Tipo de estudio
De intervención
Fase
Fase 4
Rango de edad
18 años - No especificado
Sexo admitido
Todos los sexos
Voluntarios sanos
No aceptados
Participantes
300 Estimado

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Las explicaciones y la navegación están en español. Los textos proporcionados por el registro, incluidos títulos, resúmenes y criterios, se conservan en su idioma original. Puedes pedir orientación en español a WCR.

Acerca de la investigación

Management of severe diabetic ketoacidosis is based on insulin therapy, correction of metabolic disorders and fluid resuscitation. Current recommendations recommend the first-line use of isotonic saline, whose composition is unbalanced, rich in chloride and sodium compared with plasma. Administration of large volumes of isotonic saline is associated with a risk of hyperchloremic metabolic acidosis and acute renal failure. Balanced solutions (e.g. Ringer Lactate) are solutions with a more balanced electrolyte composition close to that of plasma. They could therefore enable diabetic ketoacidosis to be resolved more quickly than isotonic saline, due to a lower risk of hyperchloremic acidosis. Preliminary data suggest a potential benefit of balanced solutions for fluid resuscitation of patients with severe diabetic ketoacidosis in terms of resolution of diabetic ketoacidosis, but no randomized controlled double-blind study to date has compared balanced solution vs. isotonic saline in this context.

¿Quién podría participar?

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Inclusion Criteria:

  • Admission to emergency department or direct admission to ICU
  • Diagnosis of severe diabetic ketoacidosis requiring all the following criteria:
  • Blood or capillary glucose \> 11 mmol/L
  • Ketonemia or ketonuria \> 0
  • Venous or arterial pH \< 7.30 or venous or arterial bicarbonate \< 15 mmol/L
  • Volume of fluid administered before inclusion \<1L

Exclusion Criteria:

  • Patients \<18 years
  • Pregnant women
  • Patients under protection
  • Patients with a decision to withdraw life-sustaining therapy
  • Contraindication to isotonic saline or Ringer Lactate
  • Non-affiliation to social security
Entiende la evaluación inicial

Tratamiento, grupos y participación

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Asignación
Asignación al azar
Enmascaramiento
Enmascaramiento cuádruple
Isotonic saline

No informado en este registro.

Drug: Fluid resuscitation with isotonic saline only

Ringer Lactate

No informado en este registro.

Drug: Fluid resuscitation with Ringer Lactate

Fluid resuscitation with isotonic saline only DRUG

Isotonic saline only will be used for fluid resuscitation in the first 48 hours of treatment, according to the protocol of English guidelines:

  • During the first hour of treatment:
  • In the event of systolic arterial hypotension (SAP\<90mmHg): administration of 500 mL over 15 minutes, renewable once, then administration of 1L over 1 hour.
  • In the absence of systolic arterial hypotension (SAP\>90mmHg): administration of 1L over 1 hour.
  • Between 60 minutes and 8 hours of treatment :
  • 1L over 2 hours, repeated once, then 1L over 4 hours
  • Adjust fluid resuscitation according to clinical tolerance
  • After the first 8 hours:
  • 1L over 4h then 1L over 6h
  • Clinical re-evaluation according to standard of care in participating centers
Fluid resuscitation with Ringer Lactate DRUG

Ringer Lactate only will be used for fluid resuscitation in the first 48 hours of treatment, according to the protocol of English guidelines:

  • During the first hour of treatment:
  • In the event of systolic arterial hypotension (SAP\<90mmHg): administration of 500 mL over 15 minutes, renewable once, then administration of 1L over 1 hour.
  • In the absence of systolic arterial hypotension (SAP\>90mmHg): administration of 1L over 1 hour.
  • Between 60 minutes and 8 hours of treatment :
  • 1L over 2 hours, repeated once, then 1L over 4 hours
  • Adjust fluid resuscitation according to clinical tolerance
  • After the first 8 hours:
  • 1L over 4h then 1L over 6h
  • Clinical re-evaluation according to standard of care in participating centers
Prepara tus preguntas

Qué evalúan los investigadores

Estas medidas indican qué se estudia. No prueban que un tratamiento funcione.

Medidas principales

Resolution of diabetic ketoacidosis

Plazo: at 24 hours

Compare fluid resuscitaiton with Ringer Lactate to isotonic saline on the resolution of diabetic ketoacidosis at 24 hours from admission to Intensive Care Unit (ICU) in patients with severe diabetic ketoacidosis.

Resolution of ketoacidosis allowing discharge from ICU, defined as the proportion of patients with the following three criteria at 24 hours from ICU admission :

1. capillary or blood glucose \< 11 mmol/L
2. ketonemia \< 0.6 mmol/l
3. venous or arterial pH ≥ 7,30 or venous or arterial bicarbonate ≥ 18 mmol/L

Medidas secundarias

Speed of resolution of metabolic disorders

Plazo: at 48 hours

Compare fluid resuscitation with Ringer Lactate and isotonic saline solution on the speed of resolution of metabolic disorders in patients admitted to ICU for severe diabetic ketoacidosis.

Proportion of patients and number of hours ("Resolution free hours") within 48 hours of ICU admission with the following three criteria:

1. capillary or blood glucose \< 11 mmol/L
2. ketonemia \< 0.6 mmol/l
3. venous or arterial pH ≥ 7,30 or venous or arterial bicarbonate ≥ 18 mmol/L

Time of resolution of metabolic disorders

Plazo: at 48 hours

Compare fluid resuscitation with Ringer Lactate and isotonic saline solution on the speed of resolution of metabolic disorders in patients admitted to ICU for severe diabetic ketoacidosis.

Time (in hours) from ICU admission to obtain one of the following three criteria:

1. capillary or blood glucose \< 11 mmol/L
2. ketonemia \< 0.6 mmol/l
3. venous or arterial pH ≥ 7,30 or venous or arterial bicarbonate ≥ 18 mmol/L

Assess the metabolic tolerance of Ringer Lactate compared to isotonic saline solution

Plazo: through the end of study average 24 months

Assess the metabolic tolerance of Ringer Lactate compared to isotonic saline solution in patients admitted to ICU for severe diabetic ketoacidosis.

Occurrence of serious metabolic disorders during ICU stay, defined as :

1. Kalemia \< 3 mmol/L
2. Natremia \> 145 mmol/L
3. Chloremia \> 110 mmol/L
4. Phosphoremia \< 0.70 mmol/L
5. Blood glucose \< 3.8 mmol/L (i.e. 0.80 g/L)
6. Persistent ketonemia/ketonuria 24 hours after ICU admission 2. Nature and volume (in liters) of fluid administered before inclusion and during the study period in each group 3. Protocol compliance (expressed as % of volume administered in each group)

Assess the impact of Ringer lactate compared with isotonic saline on renal, neurological and cardiac complications

Plazo: at 28 days

To assess the impact of Ringer lactate compared with isotonic saline on renal, neurological and cardiac complications during ICU stay and outcomes of patients admitted to ICU for severe diabetic ketoacidosis.

Occurrence of adverse events during ICU stay, defined as :

1. Neurological disorders (Glasgow score)
2. Acute renal failure (KDIGO classification)
3. Cardiac disorders (supraventricular and ventricular rhythm disorders, acute coronary syndrome) 2. ICU and hospital length of stay 3. ICU mortality and Day-28 mortality

Assess the impact of Ringer lactate compared with isotonic saline on cardiac complications

Plazo: at 28 days

To assess the impact of Ringer lactate compared with isotonic saline on cardiac complications during ICU stay and outcomes of patients admitted to ICU for severe diabetic ketoacidosis.

Occurrence of adverse events during ICU stay, defined as :

  • Cardiac disorders (supraventricular and ventricular rhythm disorders, acute coronary syndrome)
  • ICU and hospital length of stay
  • ICU mortality and Day-28 mortality
Assess the impact of Ringer lactate compared with isotonic saline on renal complications

Plazo: at 28 days

To assess the impact of Ringer lactate compared with isotonic saline on renal, complications during ICU stay and outcomes of patients admitted to ICU for severe diabetic ketoacidosis.

Measure acute renal failure with KDIGO classification.

The Kidney Disease: Improving Global Outcomes (KDIGO) classification system stratifies acute kidney injury (AKI) into levels of severity, determined by changes in serum creatinine (SCr) / estimated creatinine clearance (eCCl), as well as changes in urine output. The strata of severity of AKI can be reached by meeting the criteria for changes in SCr / eCCl or changes in urine output. There are three levels of severity, with level 1 being the least severe and level 3 the most severe.

No cut-off for the study

Assess the impact of Ringer lactate compared with isotonic saline on neurological complications

Plazo: at 28 days

To assess the impact of Ringer lactate compared with isotonic saline on neurological complications during ICU stay and outcomes of patients admitted to ICU for severe diabetic ketoacidosis.

Measure Neurological disorders with Glasgow score. The Glasgow Coma Scale (GCS) is used to objectively describe the extent of impaired consciousness in all types of patients. The scale rates patients on three aspects of reactivity: eye opening, motor responses and verbal responses. It ranges from 3 (coma) to 15 (no disturbance of consciousness). No cut-off for the study.

El registro no indica resultados publicados.

Revisa las tablas completas y sus limitaciones en el registro oficial.

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Centros de investigación (1)

El estado general puede diferir del estado de un centro. Confirma la disponibilidad antes de trasladarte.

1 centros

CHU NICENice, FranceReclutando

Equipo y fechas

Patrocinador principal
Centre Hospitalier Universitaire de Nice
Inicio del estudio
26 nov 2025 Real
Finalización primaria
2027-12 Estimado
Finalización del estudio
2028-07 Estimado
Primera publicación
7 ago 2024 Real
Última actualización
10 nov 2026 Real

Contactos oficiales del estudio

Mathieu JOZWIAK, MD PhDCONTACTjozwiak.m@chu-nice.fr+33492035510
Título oficial del estudio

Comparison of Saline and Ringer Lactate in Patients With Severe Diabetic Ketoacidosis (DRINK) : a Double-blind Randomized Controlled Trial

EL PRÓXIMO PASO, CON APOYO HUMANO

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Fuente: API v2 de ClinicalTrials.gov. Patrocinadores e investigadores envían la información. La NLM no aprueba la seguridad ni la ciencia de todos los estudios registrados. Aviso del registro.

Consultado: 12 nov 2026 · Última actualización del registro: 10 nov 2026