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Hypoglycemia clinical trials

View clinical trials related to Hypoglycemia.

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NCT ID: NCT03346746 Completed - Mood Clinical Trials

Utilizing GI: Exploring an Optimum Glycaemic Profile for Cognitive Function Across the Day

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

This study provides participants with two diets that vary in their glycaemic index values (low vs. high), whilst also measuring cognitive performance and mood.

NCT ID: NCT03344185 Completed - Mood Clinical Trials

The Effect of Glycaemic Index Variation on Blood Glucose and Mood in Healthy Participants Across the Day

Start date: July 2016
Phase: N/A
Study type: Interventional

This study provided 24 healthy subjects with two diets that varied in their glycaemic index values. One condition was a low GI diet, whilst the other was a high GI diet. Glucose concentrations and mood were measured throughout each test day.

NCT ID: NCT03339453 Completed - Clinical trials for Diabetes Mellitus, Type 1

A Study of Nasal Glucagon in Participants With Type 1 Diabetes Mellitus

Start date: November 10, 2017
Phase: Phase 1
Study type: Interventional

The purpose of this study is to compare a needle-free treatment of hypoglycemia with nasal glucagon (study drug) to a marketed glucagon administered by the intramuscular (IM) route, in participants with type 1 diabetes mellitus (T1DM).

NCT ID: NCT03286816 Completed - Clinical trials for Type 1 Diabetes Mellitus With Hypoglycemia

The Effect of Intravenous Lactate on Brain Lactate Concentrations During Hypoglycemia

Start date: November 2016
Phase: N/A
Study type: Interventional

Patients with type 1 diabetes (T1DM) who are unable to perceive symptoms of hypoglycemia, referred to as impaired awareness of hypoglycemia (IAH), are at very high risk of severe hypoglycemia. IAH affects approximately 25% of patients with T1DM. Brain lactate may be involved in the development of IAH. A recent study indicated increased brain lactate utilization during hypoglycemia in T1DM patients with IAH, which did not occur in patients with normal awareness of hypoglycemia (NAH). Conversely, administration of lactate to patients with NAH has been shown to attenuate counterregulatory hormone responses to and symptomatic awareness of hypoglycemia, thus causing a situation that resembles IAH. It has, however, not been demonstrated whether the excess of lactate is actually taken up or metabolized by the brain, and if so whether this occurs under euglycemic or hypoglycemic conditions or both. This project consists of two related studies. The objective of part 1 is to investigate the effect of elevated plasma lactate levels that are sufficient to impair awareness of hypoglycemia on brain lactate concentrations during euglycemia and hypoglycemia in T1DM patients with NAH. The objective of part 2 is to compare the effect of exogenous lactate on brain lactate concentrations between T1DM patients with NAH and T1DM patients with IAH. Furthermore, this study aims to determine the effect of acute hypoglycemia on the inflammatory function and composition of peripheral blood mononuclear cells.

NCT ID: NCT03255629 Completed - Clinical trials for Post-bariatric Hypoglycemia

Closed-Loop Glucagon Pump for Treatment of Post-Bariatric Hypoglycemia

Start date: September 19, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

To assess the efficacy of a closed loop glucagon system to prevent and treat hypoglycemia occurring in patients with Post-Bariatric Hypoglycemia (PBH) in response to meals and exercise.

NCT ID: NCT03252704 Completed - Glucose, High Blood Clinical Trials

Post-prandial Glycemic Response to Fiber in Healthy Adults

Start date: March 31, 2016
Phase: N/A
Study type: Interventional

This randomized, double-blind, comparator controlled trial evaluated the blood glucose and insulin responses in healthy adults, after consuming a high fiber or low fiber muffin top.

NCT ID: NCT03246243 Terminated - Hypoglycemia Clinical Trials

Quantitative Assessment of Sucking for Early Diagnosis of Brain Injury in Infants at High Risk

Start date: March 29, 2017
Phase:
Study type: Observational

The main goal of this study is to quantitatively assess the sucking and feeding activity of infants at high risk of neurological impairment (preterm infants and term infants at risk of abnormal neurodevelopment) during oral sucking and feeding and correlate it with their underlying neurological impairment for the early diagnosis of brain injury.

NCT ID: NCT03241706 Active, not recruiting - Clinical trials for Hypoglycemia; Iatrogenic

Liver Glycogen and Hypoglycemia in Humans

Start date: August 2, 2018
Phase: Phase 1
Study type: Interventional

The purpose of this research study is to learn more about how sugar levels in the liver affect the ability of people both with and without type 1 diabetes. People with type 1 diabetes do not make their own insulin, and are therefore required to give themselves injections of insulin in order to keep their blood sugar under control. However, very often people with type 1 diabetes give themselves too much insulin and this causes their blood sugar to become very low, which can have a negative impact on their health. When the blood sugar becomes low, healthy people secrete hormones such as glucagon and epinephrine (i.e., adrenaline), which restore the blood sugar levels to normal by increasing liver glucose production into the blood. However, in people with type 1 diabetes, the ability to release glucagon and epinephrine is impaired and this reduces the amount of sugar the liver is able to release. People with type 1 diabetes also have unusually low stores of sugar in their livers. It has been shown in animal studies that when the amount of sugar stored in the liver is increased, it increases the release of glucagon and epinephrine during insulin-induced hypoglycemia. In turn, this increase in hormone release boosts liver sugar production. However, it is not known if increased liver sugar content can influence these responses in people with and without type 1 diabetes. In addition, when people with type 1 diabetes do experience an episode of low blood sugar, it impairs their responses to low blood sugar the next day. It is also unknown whether this reduction in low blood sugar responses is caused by low liver sugar levels. The investigators want to learn more about how liver sugar levels affect the ability to respond to low blood sugar.

NCT ID: NCT03234491 Completed - Clinical trials for Post-Prandial Hypoglycemia

Improving Post-Prandial Blood Glucose Control With Afrezza During Closed-Loop Therapy

Start date: November 22, 2017
Phase: Phase 1
Study type: Interventional

The study will be conducted in two phases; an in-patient meal study phase (Phase I) and an outpatient home study (Phase II). The two phase study design is chosen to enhance safety by testing the Afrezza Closed-Loop (CL) system in controlled in-clinic setting under study staff supervision before it could be investigated at the outpatient home setting. Phase II will not begin without the establishment of safety in Phase I.

NCT ID: NCT03217175 Terminated - Clinical trials for Type 1 Diabetes Mellitus

Efficacy of Glucagon In the Prevention of Hypoglycemia During Mild Exercise

Start date: August 18, 2017
Phase: N/A
Study type: Interventional

The study will consist of two study arms. Each arm will include a 24-96 hour outpatient run-in period prior to their exercise visit wearing the bi-hormonal bionic pancreas. In random order subjects will then complete two approximately 5-hour exercise visits, one wearing the bi-hormonal bionic pancreas and one wearing the insulin-only bionic pancreas.