Post-bariatric HypoglycaemiaPBH ForecastNCT05250271
Forecasting and Preventing Post-Bariatric Hypoglycaemia WP 2
A study testing 15 g dextrose, 5 g dextrose and Protein bar in people with Post-bariatric Hypoglycaemia and Roux-en-Y Gastric Bypass, run by Lia Bally at 1 site in Switzerland.
Trial summary
The overall aim of this study is to develop a sustainable hypoglycemia correction strategy. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Post-bariatric Hypoglycaemia, Roux-en-Y Gastric Bypass
- What is being tested?
- 15 g dextrose, 5 g dextrose and Protein bar
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 8 participants
- Where
- 1 siteSwitzerland
- Study dates
- 18 Jan 2022to 26 Jul 2022
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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
Who cannot join
- 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.
Trial locations and contacts
1 site in 1 country.
Switzerland1 site
Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism (UDEM), Inselspital, Bern University Hospital
Bern, Canton of Bern, 3010
About this study
Official title: Forecasting and Preventing Post-Bariatric Hypoglycaemia (Work Package 2)
The overall aim of this study is to develop a sustainable hypoglycemia correction strategy.
Read the 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).
- Being tested
- 15 g dextrose, 5 g dextrose, Protein bar
- Keywords
- Continuous Glucose Monitoring
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
15 g dextroseOther
15 g dextrose tablets
5 g dextroseOther
5 g dextrose tablets
Protein barOther
5 g carbohydrates + 10 g protein
| Study group | Role | What they receive |
|---|---|---|
| Treatment sequence 1 | Other | Sequence of the treatments: Glucose (15g) - Glucose (5g) -Protein bar Receives: Other: 15 g dextrose; Other: 5 g dextrose; Other: Protein bar |
| Treatment sequence 2 | Other | Sequence of the treatments: Glucose (15g) - Protein bar - Glucose (5g) Receives: Other: 15 g dextrose; Other: 5 g dextrose; Other: Protein bar |
| Treatment sequence 3 | Other | Sequence of the treatments: Glucose (5g) - Glucose (15g) - Protein bar Receives: Other: 15 g dextrose; Other: 5 g dextrose; Other: Protein bar |
| Treatment sequence 4 | Other | Sequence of the treatments: Glucose (5g) - Protein bar - Glucose (15g) Receives: Other: 15 g dextrose; Other: 5 g dextrose; Other: Protein bar |
| Treatment sequence 5 | Other | Sequence of the treatments: Protein bar - Glucose (15g) - Glucose (5g) Receives: Other: 15 g dextrose; Other: 5 g dextrose; Other: Protein bar |
| Treatment sequence 6 | Other | Sequence of the treatments: Protein bar - Glucose (5g) - Glucose (15g) Receives: Other: 15 g dextrose; Other: 5 g dextrose; Other: Protein bar |
What is being measured
The primary outcome is the main question the study is designed to answer.
Time in glucose target range
The primary endpoint is time in glucose target range (plasma glucose 3.9-5.5 mmol/L).
Measured: During 40 minutes after hypoglycaemia correction
Secondary outcomes (13)
Percentage of time with plasma glucose <3.0 mmol/L
Units: %
Measured: During 40 minutes after hypoglycaemia correction
Percentage of time with plasma glucose <3.9 mmol/L
Units: %
Measured: During 40 minutes after hypoglycaemia correction
Percentage of time with plasma glucose >5.5 mmol/L
Units: %
Measured: During 40 minutes after hypoglycaemia correction
Percentage of time with plasma glucose >10.0 mmol/L
Units: %
Measured: During 40 minutes after hypoglycaemia correction
Percentage of time with sensor glucose <3.0 mmol/L
The sensor glucose values will be adjusted to plasma glucose to increase accuracy
Measured: During 150 minutes after hypoglycaemia correction
Percentage of time with sensor glucose <3.9 mmol/L
The sensor glucose values will be adjusted to plasma glucose to increase accuracy
Measured: During 150 minutes after hypoglycaemia correction
Percentage of time with sensor glucose >5.5 mmol/L
The sensor glucose values will be adjusted to plasma glucose to increase accuracy
Measured: During 150 minutes after hypoglycaemia correction
Percentage of time with sensor glucose >10.0 mmol/L
The sensor glucose values will be adjusted to plasma glucose to increase accuracy
Measured: During 150 minutes after hypoglycaemia correction
Peak plasma glucose
Peak plasma glucose (mmol/L)
Measured: Until 40 minutes after inital hypoglycaemia correction or 180 minutes after meal intake (the later timepoint of the two)
Time to euglycaemia
Time to euglycaemia after hypoglycaemia correction (plasma glucose ≥3.9 mmol/L)
Measured: Until 40 minutes after inital hypoglycaemia correction or 180 minutes after meal intake (the later timepoint of the two)
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)
Measured: During 150 minutes after hypoglycaemia correction
Insulin
Serum insulin concentration
Measured: 15 minutes after hypoglycaemia correction
Glucagon
Serum glucagon concentration
Measured: 15 minutes after hypoglycaemia correction
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Feb 2022
- Study start18 Jan 2022
- Primary completion26 Jul 2022
- Study completion26 Jul 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Post-bariatric HypoglycaemiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Crossover
- Model description
- 3-period crossover design
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 8 participants (actual)
Sponsor and investigators
- Lead sponsor
- Lia Bally
- Sponsor type
- University, hospital or other
- Collaborators
- University of Padova
- Responsible party
- Sponsor-investigator, Lia Bally, Insel Gruppe AG, University Hospital Bern
- Investigators
- Lia Bally, Prof. Dr. med. et phil., Principal investigator, Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism, lnselspital, Bern University Hospital, University of Bern
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05250271
- Sponsor's protocol ID
- PBH Forecast (WP 2)
- Acronym
- PBH Forecast
- Status last verified
- Dec 2022
- First submitted
- 14 Jan 2022
- Last updated
- 7 Dec 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: All IPD that underlie results in a publication will be available to other researchers.
Study at a glance
From the registry record, last updated by the sponsor on 7 Dec 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Forecasting and Preventing Post-Bariatric Hypoglycaemia (Work Package 2)
- ClinicalTrials.gov ID
- NCT05250271
- Acronym / sponsor ID
- PBH Forecast / PBH Forecast (WP 2)
- Keywords
- Continuous Glucose Monitoring
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 8 participants (actual)
- Lead sponsor
- Lia BallyUniversity, hospital or other
- Collaborators
- University of Padova
- Study start
- 18 Jan 2022 (actual)
- Primary completion
- 26 Jul 2022 (actual)
- Study completion
- 26 Jul 2022 (actual)
- First posted
- 22 Feb 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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).
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Single blind (participant)
- Number of arms
- 6
- Model description
- 3-period crossover design
| Arm | Type | Receives |
|---|---|---|
| Treatment sequence 1 | Other | Other: 15 g dextrose, Other: 5 g dextrose, Other: Protein barSequence of the treatments: Glucose (15g) - Glucose (5g) -Protein bar |
| Treatment sequence 2 | Other | Other: 15 g dextrose, Other: 5 g dextrose, Other: Protein barSequence of the treatments: Glucose (15g) - Protein bar - Glucose (5g) |
| Treatment sequence 3 | Other | Other: 15 g dextrose, Other: 5 g dextrose, Other: Protein barSequence of the treatments: Glucose (5g) - Glucose (15g) - Protein bar |
| Treatment sequence 4 | Other | Other: 15 g dextrose, Other: 5 g dextrose, Other: Protein barSequence of the treatments: Glucose (5g) - Protein bar - Glucose (15g) |
| Treatment sequence 5 | Other | Other: 15 g dextrose, Other: 5 g dextrose, Other: Protein barSequence of the treatments: Protein bar - Glucose (15g) - Glucose (5g) |
| Treatment sequence 6 | Other | Other: 15 g dextrose, Other: 5 g dextrose, Other: Protein barSequence of the treatments: Protein bar - Glucose (5g) - Glucose (15g) |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- 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
Key exclusion criteria (5 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| 15 g dextrose15 g dextrose tablets | Other | Treatment sequence 1, Treatment sequence 2, Treatment sequence 3, Treatment sequence 4, Treatment sequence 5, Treatment sequence 6 |
| 5 g dextrose5 g dextrose tablets | Other | Treatment sequence 1, Treatment sequence 2, Treatment sequence 3, Treatment sequence 4, Treatment sequence 5, Treatment sequence 6 |
| Protein bar5 g carbohydrates + 10 g protein | Other | Treatment sequence 1, Treatment sequence 2, Treatment sequence 3, Treatment sequence 4, Treatment sequence 5, Treatment sequence 6 |
Primary outcome
Time in glucose target range
Time frame: During 40 minutes after hypoglycaemia correction
The primary endpoint is time in glucose target range (plasma glucose 3.9-5.5 mmol/L).
13 secondary outcomes
Percentage of time with plasma glucose <3.0 mmol/L
Time frame: During 40 minutes after hypoglycaemia correction
Percentage of time with plasma glucose <3.9 mmol/L
Time frame: During 40 minutes after hypoglycaemia correction
Percentage of time with plasma glucose >5.5 mmol/L
Time frame: During 40 minutes after hypoglycaemia correction
Percentage of time with plasma glucose >10.0 mmol/L
Time frame: During 40 minutes after hypoglycaemia correction
Percentage of time with sensor glucose <3.0 mmol/L
Time frame: During 150 minutes after hypoglycaemia correction
Percentage of time with sensor glucose <3.9 mmol/L
Time frame: During 150 minutes after hypoglycaemia correction
Percentage of time with sensor glucose >5.5 mmol/L
Time frame: During 150 minutes after hypoglycaemia correction
Percentage of time with sensor glucose >10.0 mmol/L
Time frame: During 150 minutes after hypoglycaemia correction
Peak plasma glucose
Time frame: Until 40 minutes after inital hypoglycaemia correction or 180 minutes after meal intake (the later timepoint of the two)
Time to euglycaemia
Time frame: Until 40 minutes after inital hypoglycaemia correction or 180 minutes after meal intake (the later timepoint of the two)
Rebound hypoglycaemia
Time frame: During 150 minutes after hypoglycaemia correction
Insulin
Time frame: 15 minutes after hypoglycaemia correction
Glucagon
Time frame: 15 minutes after hypoglycaemia correction
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 7 Dec 2022.
- Individual participant dataSharing planned: Yes. All IPD that underlie results in a publication will be available to other researchers.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Lia Bally, Prof. Dr. med. et phil. principal investigator
Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism, lnselspital, Bern University Hospital, University of Bern
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing 15 g dextrose, 5 g dextrose and Protein bar in people with Post-bariatric Hypoglycaemia and Roux-en-Y Gastric Bypass, run by Lia Bally at 1 site in Switzerland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 7 Dec 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Time in glucose target range (time frame: During 40 minutes after hypoglycaemia correction). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Dec 2022.