Clinical Trials Logo

Hyperinsulinism clinical trials

View clinical trials related to Hyperinsulinism.

Filter by:

NCT ID: NCT05088798 Recruiting - Hyperinsulinism Clinical Trials

Utility of 18FDOPA PET/MRI for Focal Hyperinsulinism

18FDOPA HI
Start date: September 10, 2020
Phase: Phase 2
Study type: Interventional

The purpose of the study is to provide access to 18F-DOPA PET to patients at Washington University and assess the utility of 18F-DOPA PET/MRI as a preoperative tool to detect and localize focal lesions in the pancreas that are causing hyperinsulinism.

NCT ID: NCT04744896 Recruiting - Clinical trials for Polycystic Ovary Syndrome

Effects Of Combined Cryolipolysis And High Intensity Interval Training On Insulin Resistance And Body Composition In Polycystic Ovarian Patients

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

this study will be carried to investigate the effect of cryolipolysis and high intensity interval training on insulin resistance and body composition in pco women

NCT ID: NCT04732416 Recruiting - Clinical trials for Congenital Hyperinsulinism

HM15136 Treatment for 8 Weeks in Subjects Aged ≥2 Years With Congenital Hyperinsulinism (CHI)

Start date: October 28, 2021
Phase: Phase 2
Study type: Interventional

This study is designed to evaluate the safety, tolerability, pharmacokinetics (PK), and efficacy of HM15136 when used as add-on therapy in subjects with CHI with persistent hypoglycemia while on standard of care treatment (SoC). HM15136 will be administered once weekly in multiple doses to subjects in multiple age including pediatric to find appropriate exposure-response data.

NCT ID: NCT04706910 Recruiting - Parkinson Disease Clinical Trials

18F-DOPA II - PET Imaging Optimization

Start date: January 20, 2021
Phase: Phase 3
Study type: Interventional

A single centre non-randomized, non-blinded phase III prospective cohort study of 18F-DOPA PET/CT imaging in specific patient populations: 1. Pediatric patients (less than 18 years old) with congenital hyperinsulinism. 2. Pediatric patients (less than 18 years old) with neuroblastoma. 3. Pediatric (less than 18 years old) or Adult patients (18 or older) with known or clinically suspected neuroendocrine tumor. 4. Adult patients (18 or older) with a clinical suspicion of Parkinson's disease or Lewy body dementia. 5. Pediatric (less than 18 years old) or Adult patients (18 or older) with brain tumors. Image optimization (the primary study objective) and gallbladder activity pattern (the secondary objective) will be evaluated.

NCT ID: NCT04309071 Recruiting - Insulin Resistance Clinical Trials

Saliva Insulin Responses to a Standardized Meal Tolerance Test in Humans

Start date: January 4, 2019
Phase: N/A
Study type: Interventional

Recent evidence suggests that hyperinsulinemia (i.e., elevated insulin levels) is the primary causative factor in obesity. Insulin promotes fat storage and prevents fat breakdown, suggesting that weight loss would be optimized if insulin levels are managed and kept low. Understanding how different foods impact insulin levels could therefore aid in personalized weight loss (or weight maintenance) advice. It has been shown that salivary insulin can track plasma insulin following different meals and can delineate between lean and obese people. Thus, it was suggested that salivary insulin could be a potential surrogate for plasma insulin. The purpose of this study is to measure fasting saliva insulin, and salivary insulin responses to a standardized meal tolerance test in individuals with different body mass index (BMI).

NCT ID: NCT04205604 Recruiting - Clinical trials for Congenital Hyperinsulinism

18FluoroLDOPA PET Imaging for the Detection and Localization of Focal Congenital Hyperinsulinism

DOPA PET
Start date: November 3, 2016
Phase: Phase 2
Study type: Interventional

The goal of this project is to determine the role of FDOPA/PET as a pre-operative diagnostic imaging procedure for differentiating focal and diffuse forms of congenital hyperinsulinism and locating focal lesions in the pancreas to guide surgical resection.

NCT ID: NCT04118374 Recruiting - Clinical trials for Diabetes Mellitus, Type 1

A Study to Determine Iatrogenic Hyperinsulinemia's Contribution to Insulin Resistance and Endothelial Dysfunction in Type 1 Diabetes

Start date: March 29, 2019
Phase: N/A
Study type: Interventional

The investigators will test the hypothesis that reducing insulin doses using a low carbohydrate diet (LCD) will be associated with with improved insulin sensitivity (Aim 1) and blood vessel health (Aim 2).

NCT ID: NCT03768518 Recruiting - Clinical trials for Congenital Hyperinsulinism

GLP-1 Receptor Expression in CHI

GLP-1-CHI
Start date: February 7, 2018
Phase:
Study type: Observational

The primary objective is the in vivo and ex vivo investigation of the expression and distribution of the GLP-1R in the pancreas of CHI patients.

NCT ID: NCT02021604 Recruiting - Insulinoma Clinical Trials

Fluorodopa F 18 in Congenital Hyperinsulinism and Insulinoma

Start date: October 9, 2013
Phase: Phase 1
Study type: Interventional

Low blood sugars are known to cause brain damage in newborn babies. One of the most common causes of low blood sugars persisting beyond the new born period is a condition called congenital hyperinsulinism (HI). This is a disease whereby the pancreas secretes too much insulin and causes low blood sugars. Twenty to forty percent of these babies will have brain damage. There are two forms of this disease. In one form only a small part of the pancreas makes too much insulin (focal HI) and in the other, the whole pancreas make too much insulin (diffuse HI). Another very similar disease is insulinoma which occurs after birth, but also causes hyperinsulinism. If a surgeon could know which part of the pancreas has the focal lesion he could remove it and cure the patient. The purpose of this study is to investigate whether a new investigational drug called Fluorodopa F 18, when used with a PET scan, can find the focal lesion and guide the surgeon to remove it, thus curing the patient and preventing further brain damage.