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Ketosis, Diabetic clinical trials

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NCT ID: NCT05225467 Completed - Diabetes Mellitus Clinical Trials

Development of Ketoacidosis During the Perioperative Period: an Observational Study 'The DKAP Study'

DKAP
Start date: March 15, 2022
Phase:
Study type: Observational [Patient Registry]

Rationale: During perioperative period, prolonged starvation, surgical stress, acute complications (e.g. infection) and medication changes all promote ketone generation, therefore increasing the risk of ketoacidosis. At present, there is no literature concerning the ketone production in patients undergoing cardiac surgery, regardless of the diabetes status. Objectives: The objectives of this study are to explore the change in blood ketone level during the perioperative period in patients with and without diabetes, to observe the incidence of perioperative ketoacidosis, and to investigate therapy and outcome of patients with perioperative ketoacidosis.

NCT ID: NCT05118061 Completed - Diabetes Mellitus Clinical Trials

StatStrip Glucose/Ketone Meter System Ketone Evaluation

Start date: May 25, 2022
Phase:
Study type: Observational

The Nova StatStrip Glucose / Ketone Meter System is a fast, simple, whole blood system that can be used to quantify both glucose and ketones using two distinct test strips. This Protocol will describe an evaluation of the system's Ketone performance only. Ketone testing methods that quantify beta-hydroxybutyrate (β-OHB), the predominant ketone body, are used for diagnosing and monitoring ketoacidosis, a life-threatening complication of hyperglycemia. The performance of the StatStrip Ketone test strip using the Nova StatStrip Glucose / Ketone Hospital Meter System on venous and capillary whole blood will be assessed.

NCT ID: NCT04487678 Withdrawn - Ketosis, Diabetic Clinical Trials

Exogenous Ketones in People With Type 1 Diabetes

Start date: August 2023
Phase: N/A
Study type: Interventional

The aim of this pilot study is to investigate the metabolic effects of exogenous ketone ester food supplements, by assessing the change in blood acid-base balance, and the level of blood beta-hydroxy-butyrate in people with type 1 diabetes during resting conditions.