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Diabetic Ketoacidosis Diagnosis and Management

A

Akdeniz University

Status

Completed

Conditions

Brain Edema
Diabetic Ketoacidosis
Metabolic Acidosis

Treatments

Diagnostic Test: Capnography

Study type

Observational

Funder types

Other

Identifiers

NCT06327737
AKDENIZ-KAEK-916

Details and patient eligibility

About

This is the first and only study conducted on the use of capnography in children diagnosed with DKA to evaluate the initial clinical grading of DKA, monitor clinical improvement, and predict complications such as brain edema.

Full description

Purpose: In this study, the contribution of this non-invasive follow-up method to the management of DKA and the reduction of the frequency of invasive procedures was investigated in patients diagnosed with diabetic ketoacidosis (DKA) in the pediatric emergency department and followed up with capnography

Method: This study is a prospective clinical study. Between October 2020- November 2022, EtCO2 and IPI follow-up of 0-18 year-old pediatric patients diagnosed with DKA in the Pediatric Emergency Service of Akdeniz University Medical Faculty Hospital was performed by capnography. DKA diagnosis, grading, clinical follow-up and treatment termination criteria of the patients were determined according to the ISPAD 2018 Diagnosis and Treatment Guidelines. In the study; During the clinical follow-up, changes in GCS, blood glucose, vital, blood gas and capnograph parameters were examined. Demographic data were analyzed in all patients and in groups of patients who underwent DKA grading. GCS, blood gas and capnograph parameters were compared in the patient groups with DKA grading. Diagnostic test performances of blood gas and capnograph parameters were compared to detect low GCS

Enrollment

55 patients

Sex

All

Ages

15 days to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The study group consisted of pediatric patients aged 0-18 years who were diagnosed with Diabetic Ketoacidosis and applied to Akdeniz University pediatric emergency department.
  • Written consent was obtained.

Exclusion criteria

• Who did not give written consent were not included in the study.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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