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Pasireotide in the Treatment of Hypoglycemia Following Gastric Bypass Surgery

Primary Purpose

Hypoglycemia, Reactive

Status
Unknown status
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Pasireotide 0.3 MG/ML
Meal tolerance test (MTT)
Sponsored by
Zealand University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypoglycemia, Reactive focused on measuring gastric bypass, hypoglycemia, hyperinsulinemia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • RYGB operated patients with documented hypoglycemia (blood glucose <3.9 mmol/L) who have previously completed the study 'Treatment of hypoglycemia following gastric bypass surgery' (HypoGB2015)
  • Hemoglobin > 7,3 mmol/L
  • Negative human chorionic gonadotropin (hCG) urine test
  • Females of reproductive age: use of safe contraception

Exclusion Criteria:

  • Treatment for cardiovascular disease
  • Treatment with antipsychotic medication
  • Treatment for thyroid disease
  • Prior medical treatment of postprandial hyperinsulinemic hypoglycemia
  • Prior allergic reactions to the study medicine

Sites / Locations

  • Zealand University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Pasireotide75

Pasireotide150

Arm Description

75 micrograms Pasireotide 0.3 MG/ML s.c. before a meal tolerance test (MTT)

150 micrograms Pasireotide 0.3 MG/ML s.c. before a meal tolerance test (MTT)

Outcomes

Primary Outcome Measures

Changes in glucose (mmol/L) in response to a meal tolerance test (MTT)
Changes in incremental area under the curve (iAUC) for glucose, nadir glucose values, peak glucose values, time spent with glucose values in the hyperglycemic (>7.8 mmol/L) and the hypoglycemic (<3.9 mmol/L) range

Secondary Outcome Measures

Heart rate
Changes heart rate (beats/min) during the course of a meal tolerance test (MTT)
Serum insulin levels
Changes in insulin (pmol/L) in response to a meal tolerance test (MTT)
Serum C-peptide levels
Changes in C-peptide (nmol/L) in response to a meal tolerance test (MTT)
Plasma glucagon levels
Changes in glucagon (pmol/L) in response to a meal tolerance test (MTT)
Plasma GLP-1 levels
Changes in glucagon-like peptide 1 (pmol/L) in response to a meal tolerance test (MTT)
Blood pressure
Changes in blood pressure (mmHg) in response to a meal tolerance test (MTT)

Full Information

First Posted
April 19, 2018
Last Updated
July 2, 2018
Sponsor
Zealand University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03514576
Brief Title
Pasireotide in the Treatment of Hypoglycemia Following Gastric Bypass Surgery
Official Title
Pasireotide in the Treatment of Hypoglycemia Following Gastric Bypass Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2018 (Actual)
Primary Completion Date
August 1, 2018 (Anticipated)
Study Completion Date
November 1, 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zealand University Hospital

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
Yes

5. Study Description

Brief Summary
Postprandial hyperinsulinemic hypoglycemia is a well-known and potentially severe complication of Roux-en-Y gastric bypass (RYGB), and the treatment options are limited. Pasireotide has shown to be effective in preventing hypoglycemia in RYGB operated subjects, however treatment often leads to increased hyperglycemia. The purpose of this study is to investigate two doses of pasireotide that are lower than doses previously used in RYGB operated subjects with postprandial hyperinsulinemic hypoglycemia.
Detailed Description
With the growing number of RYGB operated subjects the attention on complications such as postprandial hyperinsulinemic hypoglycemia (PHH) has increased. PHH is characterized by increased glycemic variability and hypoglycemic episodes occurring 2-3 hours after a meal together with a markedly increase in insulin and glucagon-like-peptide 1 (GLP-1) levels. Symptoms vary from dizziness and palpitations to confusion, loss of consciousness and convulsions. At present there are few treatment options available for RYGB patients with PHH and most of them rely on dietary changes that are difficult to adhere to. Pasireotide has been shown to reduce hypoglycemia in RYGB operated subjects with PHH, but often leads to increased hyperglycemia as well. The purpose of the study is to investigate two doses of pasireotide in RYGB operated subjects with PHH. Each subject will undergo two meal tolerance test (MTT) preceded by either 75 µg or 150 µg of pasireotide. Blood samples will be collected throughout the meal test at predefined time points and will be analyzed for glucose, insulin, C-peptide, GLP-1 and glucagon levels.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypoglycemia, Reactive
Keywords
gastric bypass, hypoglycemia, hyperinsulinemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
5 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Pasireotide75
Arm Type
Experimental
Arm Description
75 micrograms Pasireotide 0.3 MG/ML s.c. before a meal tolerance test (MTT)
Arm Title
Pasireotide150
Arm Type
Experimental
Arm Description
150 micrograms Pasireotide 0.3 MG/ML s.c. before a meal tolerance test (MTT)
Intervention Type
Drug
Intervention Name(s)
Pasireotide 0.3 MG/ML
Other Intervention Name(s)
Signifor
Intervention Description
See arm description
Intervention Type
Diagnostic Test
Intervention Name(s)
Meal tolerance test (MTT)
Intervention Description
Subjects will consume the liquid meal at baseline and blood will be drawn for continuous blood sampling.
Primary Outcome Measure Information:
Title
Changes in glucose (mmol/L) in response to a meal tolerance test (MTT)
Description
Changes in incremental area under the curve (iAUC) for glucose, nadir glucose values, peak glucose values, time spent with glucose values in the hyperglycemic (>7.8 mmol/L) and the hypoglycemic (<3.9 mmol/L) range
Time Frame
From 20 minutes prior to a liquid test meal to 180 minutes following the meal ingestion
Secondary Outcome Measure Information:
Title
Heart rate
Description
Changes heart rate (beats/min) during the course of a meal tolerance test (MTT)
Time Frame
From 20 minutes prior to a liquid test meal to 180 minutes following the meal ingestion
Title
Serum insulin levels
Description
Changes in insulin (pmol/L) in response to a meal tolerance test (MTT)
Time Frame
From 20 minutes prior to a liquid test meal to 180 minutes following the meal ingestion
Title
Serum C-peptide levels
Description
Changes in C-peptide (nmol/L) in response to a meal tolerance test (MTT)
Time Frame
From 20 minutes prior to a liquid test meal to 180 minutes following the meal ingestion
Title
Plasma glucagon levels
Description
Changes in glucagon (pmol/L) in response to a meal tolerance test (MTT)
Time Frame
From 20 minutes prior to a liquid test meal to 180 minutes following the meal ingestion
Title
Plasma GLP-1 levels
Description
Changes in glucagon-like peptide 1 (pmol/L) in response to a meal tolerance test (MTT)
Time Frame
From 20 minutes prior to a liquid test meal to 180 minutes following the meal ingestion
Title
Blood pressure
Description
Changes in blood pressure (mmHg) in response to a meal tolerance test (MTT)
Time Frame
From 20 minutes prior to a liquid test meal to 180 minutes following the meal ingestion

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: RYGB operated patients with documented hypoglycemia (blood glucose <3.9 mmol/L) who have previously completed the study 'Treatment of hypoglycemia following gastric bypass surgery' (HypoGB2015) Hemoglobin > 7,3 mmol/L Negative human chorionic gonadotropin (hCG) urine test Females of reproductive age: use of safe contraception Exclusion Criteria: Treatment for cardiovascular disease Treatment with antipsychotic medication Treatment for thyroid disease Prior medical treatment of postprandial hyperinsulinemic hypoglycemia Prior allergic reactions to the study medicine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Caroline C Øhrstrøm, MD
Organizational Affiliation
Department of Medicine, Zealand University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zealand University Hospital
City
Køge
ZIP/Postal Code
4600
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No

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Pasireotide in the Treatment of Hypoglycemia Following Gastric Bypass Surgery

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