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Hypoglycemia clinical trials

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NCT ID: NCT05560789 Completed - Physical Activity Clinical Trials

The Effect of Physical Activity in Individuals With Post-bariatric Hypoglycemia

Start date: January 3, 2023
Phase: N/A
Study type: Interventional

The goal of this pilot study is to evaluate the magnitude of changes in glucose and hormone levels in response to structured exercise in the fasting state in individuals with post-bariatric hypoglycemia (PBH). This pilot study will assess the adequacy of a protocol to test the following hypotheses: (1) hypoglycemia will develop in individuals with PBH in response to exercise; (2) counterregulatory hormonal responses to hypoglycemia during exercise are impaired in individuals with PBH.

NCT ID: NCT05541939 Completed - Clinical trials for Postbariatric Hypoglycemia

Effect of Mizagliflozin on Postprandial Glucose and Insulin in Post-Bariatric Hypoglycemia Subjects

Start date: September 13, 2022
Phase: Phase 2
Study type: Interventional

This clinical study will examine the safety and tolerability, as well as the effects of orally administered mizagliflozin on post prandial glucose and insulin levels in subjects diagnosed with post-bariatric hypoglycemia (PBH).

NCT ID: NCT05513404 Completed - Clinical trials for Age-Related Memory Disorders

The Scottish Fruit Study

Start date: August 15, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if new varieties of fruits grown in Scotland which can adapt better to climate change namely, honeyberries and cherries, have the same health benefits as established fruits such as raspberries. To do this we will investigate the effects of consuming honeyberries, cherries, and raspberries on short term changes in blood glucose, and on short term memory.

NCT ID: NCT05470842 Completed - Diabetes Clinical Trials

How Common is Hypoglycaemia in Older People With Diabetes Who Fall?

Start date: June 6, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to use 24 hour continuous glucose monitoring in older patients with diabetes who present with symptoms of falls, or dizziness, or confusion, that may indicate hypoglycaemia.

NCT ID: NCT05457400 Completed - Sugar; Blood, Low Clinical Trials

ENSO 16 - Study in Healthy Subjects

Start date: April 28, 2022
Phase: Phase 1
Study type: Interventional

The objective of this study is to evaluate differences in glucose metabolism parameters after oral administration of 30g glucose or 30g ENSO16. Blood samples will be be collected from 15 male or female subjects at defined time points (0 - 15 - 30 - 45 - 60 - 90 - 120 - 180 minutes; 3 min at each time point). Individual plasma glucose, insulin and C-peptide concentrations are going to be evaluated and statistically assessed. Subjects will also be asked to complete a questionnaire regarding their digestion after oral intake of ENSO 16 or glucose defined timepoints.

NCT ID: NCT05395000 Completed - Clinical trials for Diabetes Mellitus, Type 1

Comparison of Ease of Use and Acceptability of Intranasal and Injectable Glucagon Among Providers Administering it to Children or Adolescents With Type 1 Diabetes (BETTER-ING)

Start date: March 19, 2021
Phase: N/A
Study type: Interventional

Background : The benefits of good glycemic control are clearly established. However, achieving glycemic targets comes at the expense of the risk of hypoglycemia. Repeated episodes of severe hypoglycemia can affect long-term cognitive function, especially in developing brains. Fear of hypoglycemia, both in children and their parents, has an impact on participation in physical activity, quality of life and optimal diabetes control. During an episode of severe hypoglycemia, i.e., when accompanied by severe cognitive dysfunction requiring assistance from others, it is impossible to administer oral glucose. Glucagon administration is particularly useful in this situation, as it rapidly raises blood glucose levels and restores consciousness. Injectable glucagon was the only form approved in Canada prior to 2019. A new formulation of glucagon for intranasal administration has recently been approved by Health Canada. The arrival of this formulation seems promising because of its ease of use while ensuring similar efficacy to injectable glucagon. Furthermore, the ease of learning how to use each of the devices through a simple multimedia tool is unknown. Indeed, current studies have not focused on a virtual teaching method. The latter is of particular interest in the context of a pandemic and in order to make information more accessible to a broader population that may not be present at family glucagon education (e.g., school-based caregivers). Objective : Compare the performance (time to prepare and administer, success rate) of the intranasal versus injectable glucagon administration procedure after a short video training 3 months earlier among parents/primary caregivers and school workers who may administer glucagon to children with type 1 diabetes. Secondary objectives : 1. To assess stakeholder administration procedure preferences for the two glucagon formulations in the two groups ; 2. To explore the barriers and emotional impact (fears, perceptions, stress, etc.) related to the use of intranasal and injectable glucagon in both groups; 3. Explore the participants' preferences in relation to the teaching method of administering the two forms of glucagon.

NCT ID: NCT05308095 Completed - Diabetes Clinical Trials

The HEADWIND Study - Part 4

Start date: April 13, 2022
Phase: N/A
Study type: Interventional

To analyse driving behavior of individuals with type 1 diabetes in eu- and mild hypoglycaemia while driving in a real car. Based on the in-vehicle variables, the investigators aim at establishing algorithms capable of discriminating eu- and hypoglycaemic driving patterns using machine learning classifiers.

NCT ID: NCT05250271 Completed - Clinical trials for Roux-en-Y Gastric Bypass

Forecasting and Preventing Post-Bariatric Hypoglycaemia WP 2

PBH Forecast
Start date: January 18, 2022
Phase: N/A
Study type: Interventional

The overall aim of this study is to develop a sustainable hypoglycemia correction strategy.

NCT ID: NCT05212207 Completed - Clinical trials for Roux-en-Y Gastric Bypass

Forecasting and Preventing Post-Bariatric Hypoglycaemia WP 1

PBH Forecast
Start date: January 18, 2022
Phase:
Study type: Observational

The overall aim of this study is to prevent hypoglycemic events in patients with hypoglycemia after a meal and to develop a sustainable hypoglycemia correction strategy.

NCT ID: NCT05183191 Completed - Diabetes Clinical Trials

The HEADWIND Study - Part 3

Start date: November 29, 2021
Phase: N/A
Study type: Interventional

To analyse driving behavior of individuals with type 1 diabetes in eu- and mild hypoglycaemia using a validated research driving simulator. Based on the driving variables provided by the simulator the investigators aim at establishing algorithms capable of discriminating eu- and hypoglycemic driving patterns using machine learning classifiers.