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Clinical Trial Summary

The goal of this clinical trial is to learn if continuous glucose monitoring works to treat postprandial hypoglycaemia in patients who have undergone bariatric 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 bariatric surgery? Researchers will compare continuous glucose monitoring to usual care to see if continuous glucose monitoring works to treat postprandial hypoglycaemia. Participants will: - Use a continuous glucose monitor for 5 weeks or use no continuous glucose monitor for 5 weeks. During week 6 both groups will wear a continuous glucose monitor, but the patients who have not been wearing a continuous glucose monitor will wear a blinded continuous glucose monitor. - Visit the clinic 3 times. - Register symptoms of hypoglycaemia, answer questionnaires, keep a food diary, measure weight and body composition and take blood samples.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT06468865
Study type Interventional
Source Sykehuset i Vestfold HF
Contact Heidi Borgeraas, PhD
Phone 004746707000
Email heibor@siv.no
Status Recruiting
Phase N/A
Start date June 17, 2024
Completion date December 31, 2026