Glucose Monitoring in Treatment of Postprandial Hypoglycemia After Gastric Bypass Surgery

Recruiting N/A Interventional Study
Hypoglycemia Non-Diabetic Gastric Bypass Surgery
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
100 (estimated)
Sponsor
Sykehuset i Vestfold HF · Other
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About This Trial
The goal of this clinical trial is to learn if continuous glucose monitoring works to treat postprandial hypoglycaemia in patients who have undergone gastric bypass surgery. The main question it aims to answer is: • Is continuous glucose monitoring superior to usual care for prevention of postprandial hypoglycaemia in patients with verified postprandial hypoglycaemia after gastric bypass surgery?…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Gastric bypass surgery at least 1 year ago * Age ≥18 years * Symptomatic postprandial hypoglycaemia; capillary glucose level \<3.0 mmol/L 1-4 hours after meals Exclusion Criteria: * Not able to give informed consent * Reduced compliance due to severe mental and psychiatric c…
Contacts

Heidi Borgeraas, PhD

004746707000

heibor@siv.no

CONTACT