Glycogen Storage Disease Breath Test Study
NCT03218904 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14
Last updated 2025-01-27
Summary
Glycogen storage disease type I (GSD I) caused by deficiency of glucose-6-phosphatase enzyme leading to build up of a complex sugar called glycogen in liver and low blood glucose level. Nutritional treatment involves supplying carbohydrates and uncooked cornstarch. Glycosade® (modified cornstarch) has shown promise in maintaining normal blood glucose level in GSD I. But the difficulty in nutritional treatment is determining the best type of carbohydrate to be given to avoid low blood glucose. Thus, there is a need to develop a simple test to examine glucose digestion and measure the utilization of different carbohydrates in GSD I and healthy controls.
Conditions
- Patient Compliance
- Healthy
Interventions
- DIETARY_SUPPLEMENT
-
Glucose intake
Experiment 1: study day1- single oral dose of glucose study day 2-single oral dose of glucose with U-13C-glucose
- DIETARY_SUPPLEMENT
-
Carbohydrates intake
Experiment 2:study day1- single oral dose of uncooked cornstarch study day 2- single oral dose of Glycosade®
Sponsors & Collaborators
-
Saudi Arabian Cultural Bureau, Ottawa
collaborator UNKNOWN -
Canadian Institutes of Health Research (CIHR)
collaborator OTHER_GOV -
University of British Columbia
lead OTHER
Principal Investigators
-
Rajavel Elango, PhD · University of British Columbia
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- HEALTH_SERVICES_RESEARCH
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 5 Years
- Max Age
- 35 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2017-03-17
- Primary Completion
- 2021-10-23
- Completion
- 2025-01-24
Countries
- Canada
Study Locations
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