Canagliflozin in Postprandial Hyperinsulinemic Hypoglycemia (CANA-PHH-RYGB) (CANA-PHH-RYGB)
Primary Purpose
Postprandial Hypoglycemia
Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Canagliflozin 300 MG Oral Tablet
Sponsored by
About this trial
This is an interventional treatment trial for Postprandial Hypoglycemia
Eligibility Criteria
Inclusion Criteria:
- Patients diagnosed with PHH following Roux-en-Y-gastric by-pass, by means of 100g Glucose OGTT. Plasma glucose <50mg/dl.
- Patients that during any time of the OGTT present at least one value of plasma glucose >200mg/dl, besides hypoglycemia
Exclusion Criteria:
- Patients unwilling to take canagliflozin 300mg
- Patients that present with PHH following other bariatric surgery techniques
Sites / Locations
- Andreea CiudinRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Patients with PHH following Roux-en-Y-gastric bypass (cases)
Healthy individuals (controls)
Arm Description
Patients diagnosed with PHH following Roux-en-Y-gastric bypass.
Healthy normoweight individuals, matched by age and gender with the cases.
Outcomes
Primary Outcome Measures
response to OGTT in basal conditions and after treatment with canagliflozin 300 mg in patients with PHH after RYGB
The OGTTis performed as follows: a solution of 100g glucose is administered at 8am after 10 hours of fasting. Plasma glucose and serum insulin were measured at minute -5, +30, +60, +120, +180 after the ingestion of the glucose solution. A first OGTT was performed in basal conditions. The control group only performed the basal OGTT. A value of plasma glucose below 50mg/dl at 60-180 minutes after the administration of the glucose solution is considered positive for PHH. The patients that additionally presented a value of plasma glucose>200mg/dl during the OGTT were selected for continuing in the study and were prescribed canagliflozin 300mg orally daily, during two weeks, and 100g glucose OGTT was repeated.
Secondary Outcome Measures
Presence of nesidioblastosis
By evaluating pancreatic response to intra-arterial calcium stimulation. The right femoral artery is catheterized with another 4.1 Fr, followed by standard pancreatic arteriography, with selective injections of nonionic contrast agent into the superior mesenteric artery, gastroduodenal artery, splenic artery and common hepatic artery. Following each selective arteriogram, 10% calcium gluconate solution is diluted with normal saline into a 5 mL bolus and injected into the selective artery at a dose of 0.010-0.025 mEq Ca2+/kg. A >2-fold gradient in insulin concentration at 30, 60, 90 or 120 seconds after the arterial calcium injection and baseline in any of the superior mesenteric artery, gastroduodenal artery, splenic artery and common hepatic artery was defined as a positive response for endogenous hyperinsulinism.
Full Information
NCT ID
NCT04720859
First Posted
January 19, 2021
Last Updated
January 26, 2021
Sponsor
Hospital Universitari Vall d'Hebron Research Institute
1. Study Identification
Unique Protocol Identification Number
NCT04720859
Brief Title
Canagliflozin in Postprandial Hyperinsulinemic Hypoglycemia (CANA-PHH-RYGB)
Acronym
CANA-PHH-RYGB
Official Title
Canagliflozin: a New Therapeutic Option in Patients That Present Postprandial Hyperinsulinemic Hypoglycemia After Roux-en-Y-gastric By-pass
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 5, 2018 (Actual)
Primary Completion Date
December 20, 2019 (Actual)
Study Completion Date
December 31, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitari Vall d'Hebron Research Institute
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Roux-en-Y gastric bypass (RYGB) is the most common surgical procedure for morbid obesity. However, it can present serious late complications, like postprandial hyperinsulinemic hypoglycemia (PHH). Recent data suggested an increase in intestinal SGLT1 after RYGB. However, there are no data on the inhibition of SLGT1 to prevent PHH in patients with prior RYBG.
Objectives: To evaluate in patients that present PHH after RYGB: a) the effect of canagliflozin 300mg on the response to 100g glucose overload (OGTT); b) the pancreatic response after intra-arterial calcium stimulation.
Material and methods: Prospective pilot study, including patients with PHH after RYGB, matched by age and gender with healthy controls. Basal OGTT and after 2-weeks of daily 300mg of canagliflozin will be performed. In addition, venous sampling after intra-arterial calcium stimulation of the pancreas will be performed.
Detailed Description
A prospective opened, placebo uncontrolled, pilot interventional study is performed at the Morbid Obesity Unit of the Vall Hebron University Hospital, including patients that have previously undergone RYGB at our site and were diagnosed with PHH. The control group comprises of healthy normoweight persons matched by age, most of them family members of patients included in the study. The OGTT is performed as follows: a solution of 100g glucose was administered at 8am after 10 hours of fasting. Plasma glucose and serum insulin are measured at minute -5, +30, +60, +120, +180 after the ingestion of the glucose solution. A first OGTT is performed in basal conditions. The control group only will perform the basal OGTT. A value of plasma glucose below 50mg/dl at 60-180 minutes after the administration of the glucose solution is considered positive for PHH. The patients that additionally present a value of plasma glucose>200mg/dl during the OGTT will be selected for continuing in the study and will be prescribed canagliflozin 300mg orally daily, during 2 weeks. After 2 weeks of canagliflozin treatment, a new OGTT will be performed and, in the patients that sign the additional inform consent, the pancreatic catheterism will be realized.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postprandial Hypoglycemia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Intervention arm in patients that present postprandial hypoglycemia following gastric by-pass and a control group of healthy subjects without intervention.
Masking
Investigator
Allocation
Non-Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Patients with PHH following Roux-en-Y-gastric bypass (cases)
Arm Type
Experimental
Arm Description
Patients diagnosed with PHH following Roux-en-Y-gastric bypass.
Arm Title
Healthy individuals (controls)
Arm Type
No Intervention
Arm Description
Healthy normoweight individuals, matched by age and gender with the cases.
Intervention Type
Drug
Intervention Name(s)
Canagliflozin 300 MG Oral Tablet
Intervention Description
Patients diagnosed with PHH following bariatric surgery by 100g glucose OGTT were prescribed 300mg canagliflozin during two weeks. 100g glucose OGTT response was evaluated after canagliflozin treatment.
Primary Outcome Measure Information:
Title
response to OGTT in basal conditions and after treatment with canagliflozin 300 mg in patients with PHH after RYGB
Description
The OGTTis performed as follows: a solution of 100g glucose is administered at 8am after 10 hours of fasting. Plasma glucose and serum insulin were measured at minute -5, +30, +60, +120, +180 after the ingestion of the glucose solution. A first OGTT was performed in basal conditions. The control group only performed the basal OGTT. A value of plasma glucose below 50mg/dl at 60-180 minutes after the administration of the glucose solution is considered positive for PHH. The patients that additionally presented a value of plasma glucose>200mg/dl during the OGTT were selected for continuing in the study and were prescribed canagliflozin 300mg orally daily, during two weeks, and 100g glucose OGTT was repeated.
Time Frame
Baseline to 180 minutes
Secondary Outcome Measure Information:
Title
Presence of nesidioblastosis
Description
By evaluating pancreatic response to intra-arterial calcium stimulation. The right femoral artery is catheterized with another 4.1 Fr, followed by standard pancreatic arteriography, with selective injections of nonionic contrast agent into the superior mesenteric artery, gastroduodenal artery, splenic artery and common hepatic artery. Following each selective arteriogram, 10% calcium gluconate solution is diluted with normal saline into a 5 mL bolus and injected into the selective artery at a dose of 0.010-0.025 mEq Ca2+/kg. A >2-fold gradient in insulin concentration at 30, 60, 90 or 120 seconds after the arterial calcium injection and baseline in any of the superior mesenteric artery, gastroduodenal artery, splenic artery and common hepatic artery was defined as a positive response for endogenous hyperinsulinism.
Time Frame
30 minutes
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients diagnosed with PHH following Roux-en-Y-gastric by-pass, by means of 100g Glucose OGTT. Plasma glucose <50mg/dl.
Patients that during any time of the OGTT present at least one value of plasma glucose >200mg/dl, besides hypoglycemia
Exclusion Criteria:
Patients unwilling to take canagliflozin 300mg
Patients that present with PHH following other bariatric surgery techniques
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Andreea Ciudin, Prof.
Phone
697817352
Ext
6591
Email
aciudin@vhebron.net
First Name & Middle Initial & Last Name or Official Title & Degree
Enzamaria Fidilio, MD
Ext
6591
Email
enzamaria.fidilio@vhir.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andreea Ciudin, Prof.
Organizational Affiliation
Vall Hebron University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Andreea Ciudin
City
Barcelona
ZIP/Postal Code
08035
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andreea Ciudin, Prof
Phone
697817352
Ext
6591
Email
aciudin@vhebron.net
First Name & Middle Initial & Last Name & Degree
Enzamaria Fidilio, MD
Ext
6591
Email
enzamaria.fidilio@vhir.org
First Name & Middle Initial & Last Name & Degree
Marta Sanchez, MD
First Name & Middle Initial & Last Name & Degree
Irene Hernandez, BS
First Name & Middle Initial & Last Name & Degree
Efrain Cordero, BS
First Name & Middle Initial & Last Name & Degree
Enzamaria Fidilio, MD
First Name & Middle Initial & Last Name & Degree
Marta Comas, Nutritionist
First Name & Middle Initial & Last Name & Degree
Carla Gonzalez, MD
First Name & Middle Initial & Last Name & Degree
Natividad Lopez, Nurse
First Name & Middle Initial & Last Name & Degree
Ramon Vilallonga, Prof
First Name & Middle Initial & Last Name & Degree
Cristina Hernandez, Prof
First Name & Middle Initial & Last Name & Degree
Rafael Simo, Prof
12. IPD Sharing Statement
Plan to Share IPD
No
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Canagliflozin in Postprandial Hyperinsulinemic Hypoglycemia (CANA-PHH-RYGB)
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