Forecasting and Preventing Post-Bariatric Hypoglycaemia WP 2 (PBH Forecast)
Primary Purpose
Post-bariatric Hypoglycaemia, Roux-en-Y Gastric Bypass
Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
15 g dextrose
5 g dextrose
Protein bar
Sponsored by
About this trial
This is an interventional supportive care trial for Post-bariatric Hypoglycaemia focused on measuring Continuous Glucose Monitoring
Eligibility Criteria
Inclusion Criteria:
- Post-bariatric surgery patients (Roux-en-Y gastric bypass) with PBH, defined as postprandial plasma or sensor glucose <3.0 mmol/L according to the International Hypoglycaemia Study Group and exclusion of other causes of hypoglycaemia
- Age ≥18 years
Exclusion Criteria:
- Inability to give informed consent as documented by signature
- Pregnant or lactating women
- Inability or contraindications to undergo the investigated intervention
- Drugs interfering with blood glucose (e.g. SGLT-2 inhibitors, acarbose) during the time of investigation
- Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc.
Sites / Locations
- Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism (UDEM), Inselspital, Bern University Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Arm Type
Other
Other
Other
Other
Other
Other
Arm Label
Treatment sequence 1
Treatment sequence 2
Treatment sequence 3
Treatment sequence 4
Treatment sequence 5
Treatment sequence 6
Arm Description
Sequence of the treatments: Glucose (15g) - Glucose (5g) -Protein bar
Sequence of the treatments: Glucose (15g) - Protein bar - Glucose (5g)
Sequence of the treatments: Glucose (5g) - Glucose (15g) - Protein bar
Sequence of the treatments: Glucose (5g) - Protein bar - Glucose (15g)
Sequence of the treatments: Protein bar - Glucose (15g) - Glucose (5g)
Sequence of the treatments: Protein bar - Glucose (5g) - Glucose (15g)
Outcomes
Primary Outcome Measures
Time in glucose target range
The primary endpoint is time in glucose target range (plasma glucose 3.9-5.5 mmol/L).
Secondary Outcome Measures
Percentage of time with plasma glucose <3.0 mmol/L
Units: %
Percentage of time with plasma glucose <3.9 mmol/L
Units: %
Percentage of time with plasma glucose >5.5 mmol/L
Units: %
Percentage of time with plasma glucose >10.0 mmol/L
Units: %
Percentage of time with sensor glucose <3.0 mmol/L
The sensor glucose values will be adjusted to plasma glucose to increase accuracy
Percentage of time with sensor glucose <3.9 mmol/L
The sensor glucose values will be adjusted to plasma glucose to increase accuracy
Percentage of time with sensor glucose >5.5 mmol/L
The sensor glucose values will be adjusted to plasma glucose to increase accuracy
Percentage of time with sensor glucose >10.0 mmol/L
The sensor glucose values will be adjusted to plasma glucose to increase accuracy
Peak plasma glucose
Peak plasma glucose (mmol/L)
Time to euglycaemia
Time to euglycaemia after hypoglycaemia correction (plasma glucose ≥3.9 mmol/L)
Rebound hypoglycaemia
Proportion of participants with rebound hypoglycaemia (plasma glucose <3.0 mmol/L following successful primary hypoglycaemia correction defined as plasma glucose ≥3.9 mmol/L)
Insulin
Serum insulin concentration
Glucagon
Serum glucagon concentration
Full Information
NCT ID
NCT05250271
First Posted
January 14, 2022
Last Updated
December 5, 2022
Sponsor
Lia Bally
Collaborators
University of Padova
1. Study Identification
Unique Protocol Identification Number
NCT05250271
Brief Title
Forecasting and Preventing Post-Bariatric Hypoglycaemia WP 2
Acronym
PBH Forecast
Official Title
Forecasting and Preventing Post-Bariatric Hypoglycaemia (Work Package 2)
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
January 18, 2022 (Actual)
Primary Completion Date
July 26, 2022 (Actual)
Study Completion Date
July 26, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Lia Bally
Collaborators
University of Padova
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The overall aim of this study is to develop a sustainable hypoglycemia correction strategy.
Detailed Description
Obesity is a major global public health concern, for which the most effective therapy is bariatric surgery. Beyond weight loss, bariatric surgery exerts powerful effects on glucose metabolism, achieving complete type 2 diabetes remission in up to 70% of cases. An exaggeration of these effects, however, can result in an increasingly recognized metabolic complication known as postprandial hyperinsulinaemic hypoglycaemia or post-bariatric hypoglycaemia (PBH). The condition manifests 1-3 years after surgery with meal-induced hypoglycaemic episodes. Emerging data suggests that PBH is more frequent than previously thought and affects approximately 30% of postoperative patients, more commonly after gastric bypass than sleeve gastrectomy. Of note, asymptomatic PBH is common, as shown in studies using continuous glucose monitoring (CGM). It is known from extensive research in people with diabetes that recurrent episodes of hypoglycaemia impair counter regulatory defences against subsequent events, predisposing patients to severe hypoglycaemia.
Despite the increasing prevalence of PBH, clinical implications in this population are still unclear. Anecdotal evidence from patients with PBH suggests a high burden for these patients due to the recurrent hypoglycaemias with possibly debilitating consequences. It is well established that even mild hypoglycaemia (plasma glucose of 3.4 mmol/L) in diabetic and non-diabetic patients impairs various cognitive domains. Of note, some of the cognitive functions remain impaired for up to 75 min, even when the hypoglycaemia is corrected. Further concerns exist from observational studies showing associations between PBH during pregnancy and poor foetal growth.
Thus, it is important to timely detect and treat hypoglycaemia with an intervention that allows quick recovery of glycaemia to a safe level, thereby alleviating symptoms and eliminating the risk of potentially hazardous sequelae. Current diabetes-inspired guidelines recommend to correct hypoglycaemia with 15-20 g fast-acting carbohydrates, preferably glucose. However, clinical experience with PBH patients shows that the rapid spikes in glycaemia following correction of hypoglycaemia with such proposed strategies may trigger rebound hypoglycaemia in PBH patients. However, hypoglycaemia correction strategies that are tailored to the specific needs of PBH do not exist currently. Previous research suggests that glucose co-ingested with amino acids induces a metabolic environment that could be favourable for PBH patients due to elevated glucagon levels. However, it currently remains speculative whether combinations of amino acids with glucose could offer more suitable and sustainable PBH correction strategies.
Given the potentially hazardous consequences of hypoglycaemia, development of hypoglycaemia management strategies to adequately predict and treat critical blood glucose levels in the PBH population are urgently needed. Such strategies have to significantly lower the burden of PBH and increase patient safety.
The overall aim or the PBH forecast project (containing 3 WPs) is to prevent hypoglycaemic events in patients with PBH and to develop a sustainable hypoglycaemia correction strategy. The primary objective of WP 2 is to test different nutritional strategies for sustainable hypoglycaemia correction (e.g. minimising time spent hypoglycaemic without causing rebound hyper- and hypoglycaemia).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-bariatric Hypoglycaemia, Roux-en-Y Gastric Bypass
Keywords
Continuous Glucose Monitoring
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
3-period crossover design
Masking
Participant
Masking Description
Participants are blinded to sensor and plasma glucose.
Allocation
Randomized
Enrollment
8 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment sequence 1
Arm Type
Other
Arm Description
Sequence of the treatments: Glucose (15g) - Glucose (5g) -Protein bar
Arm Title
Treatment sequence 2
Arm Type
Other
Arm Description
Sequence of the treatments: Glucose (15g) - Protein bar - Glucose (5g)
Arm Title
Treatment sequence 3
Arm Type
Other
Arm Description
Sequence of the treatments: Glucose (5g) - Glucose (15g) - Protein bar
Arm Title
Treatment sequence 4
Arm Type
Other
Arm Description
Sequence of the treatments: Glucose (5g) - Protein bar - Glucose (15g)
Arm Title
Treatment sequence 5
Arm Type
Other
Arm Description
Sequence of the treatments: Protein bar - Glucose (15g) - Glucose (5g)
Arm Title
Treatment sequence 6
Arm Type
Other
Arm Description
Sequence of the treatments: Protein bar - Glucose (5g) - Glucose (15g)
Intervention Type
Other
Intervention Name(s)
15 g dextrose
Intervention Description
15 g dextrose tablets
Intervention Type
Other
Intervention Name(s)
5 g dextrose
Intervention Description
5 g dextrose tablets
Intervention Type
Other
Intervention Name(s)
Protein bar
Intervention Description
5 g carbohydrates + 10 g protein
Primary Outcome Measure Information:
Title
Time in glucose target range
Description
The primary endpoint is time in glucose target range (plasma glucose 3.9-5.5 mmol/L).
Time Frame
During 40 minutes after hypoglycaemia correction
Secondary Outcome Measure Information:
Title
Percentage of time with plasma glucose <3.0 mmol/L
Description
Units: %
Time Frame
During 40 minutes after hypoglycaemia correction
Title
Percentage of time with plasma glucose <3.9 mmol/L
Description
Units: %
Time Frame
During 40 minutes after hypoglycaemia correction
Title
Percentage of time with plasma glucose >5.5 mmol/L
Description
Units: %
Time Frame
During 40 minutes after hypoglycaemia correction
Title
Percentage of time with plasma glucose >10.0 mmol/L
Description
Units: %
Time Frame
During 40 minutes after hypoglycaemia correction
Title
Percentage of time with sensor glucose <3.0 mmol/L
Description
The sensor glucose values will be adjusted to plasma glucose to increase accuracy
Time Frame
During 150 minutes after hypoglycaemia correction
Title
Percentage of time with sensor glucose <3.9 mmol/L
Description
The sensor glucose values will be adjusted to plasma glucose to increase accuracy
Time Frame
During 150 minutes after hypoglycaemia correction
Title
Percentage of time with sensor glucose >5.5 mmol/L
Description
The sensor glucose values will be adjusted to plasma glucose to increase accuracy
Time Frame
During 150 minutes after hypoglycaemia correction
Title
Percentage of time with sensor glucose >10.0 mmol/L
Description
The sensor glucose values will be adjusted to plasma glucose to increase accuracy
Time Frame
During 150 minutes after hypoglycaemia correction
Title
Peak plasma glucose
Description
Peak plasma glucose (mmol/L)
Time Frame
Until 40 minutes after inital hypoglycaemia correction or 180 minutes after meal intake (the later timepoint of the two)
Title
Time to euglycaemia
Description
Time to euglycaemia after hypoglycaemia correction (plasma glucose ≥3.9 mmol/L)
Time Frame
Until 40 minutes after inital hypoglycaemia correction or 180 minutes after meal intake (the later timepoint of the two)
Title
Rebound hypoglycaemia
Description
Proportion of participants with rebound hypoglycaemia (plasma glucose <3.0 mmol/L following successful primary hypoglycaemia correction defined as plasma glucose ≥3.9 mmol/L)
Time Frame
During 150 minutes after hypoglycaemia correction
Title
Insulin
Description
Serum insulin concentration
Time Frame
15 minutes after hypoglycaemia correction
Title
Glucagon
Description
Serum glucagon concentration
Time Frame
15 minutes after hypoglycaemia correction
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Post-bariatric surgery patients (Roux-en-Y gastric bypass) with PBH, defined as postprandial plasma or sensor glucose <3.0 mmol/L according to the International Hypoglycaemia Study Group and exclusion of other causes of hypoglycaemia
Age ≥18 years
Exclusion Criteria:
Inability to give informed consent as documented by signature
Pregnant or lactating women
Inability or contraindications to undergo the investigated intervention
Drugs interfering with blood glucose (e.g. SGLT-2 inhibitors, acarbose) during the time of investigation
Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lia Bally, Prof. Dr. med. et phil.
Organizational Affiliation
Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism, lnselspital, Bern University Hospital, University of Bern
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism (UDEM), Inselspital, Bern University Hospital
City
Bern
State/Province
BE
ZIP/Postal Code
3010
Country
Switzerland
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
All IPD that underlie results in a publication will be available to other researchers.
IPD Sharing Time Frame
After study completion, 10 years
IPD Sharing Access Criteria
Data will be shared after written inquiry and approval by the principal investigator.
Learn more about this trial
Forecasting and Preventing Post-Bariatric Hypoglycaemia WP 2
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