Treatment of Dysglycemia Using Sitagliptin in Adolescents With Cystic Fibrosis
Primary Purpose
Cystic Fibrosis
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Sitagliptin
Sponsored by
About this trial
This is an interventional diagnostic trial for Cystic Fibrosis focused on measuring cystic fibrosis, CF, CFRD, sitagliptin, incretins, GLP1, GIP, beta cell function, adolescents
Eligibility Criteria
Inclusion Criteria:
- Patients with CF between 13 and <21 yrs old
- Known impaired or indeterminate glucose tolerance (based on a prior OGTT)
- No history of CFRD
Exclusion Criteria:
- Insulin use in the last two months
- Acute pulmonary exacerbation / oral corticosteroid use in the last 6 weeks
- History of pancreatitis in the last 12 months
- Skin rashes or conditions that may affect CGM placement and wear
- Pregnancy or intent on becoming pregnant
- Patients on growth hormone therapy
- Renal insufficiency with creatinine clearance <50 ml/min (based on Schwartz formula)
Sites / Locations
- Nemours Children's Clinic
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Sitagliptin
Arm Description
Treatment with sitagliptin
Outcomes
Primary Outcome Measures
Response to sitagliptin
Baseline and stimulated C-peptide levels (using mixed meal tolerance test) before and after treatment with sitagliptin.
Response to sitagliptin
Change in glycemic variability using continuous glucose monitoring data before and after treatment with dipeptidyl peptidase-4 inhibitor.
Response to sitagliptin
Change in incretins concentrations (glucagon like peptide 1; glucose-dependent insulinotropic polypeptide) in response to study drug.
Response to sitagliptin
Change in incretin (glucagon like peptide 1; glucose-dependent insulinotropic polypeptide) concentrations in response to study drug.
Secondary Outcome Measures
Beta-cell function
Beta-cell function will be measured using mixed meal tolerance tests (MMTT) and oral glucose tolerance tests (OGTT), assessing maximum concentration and area under the curve (AUC) of glucose, insulin and c-peptide for both OGTT and MMTT.
Continuous glucose monitoring (CGM)
Baseline and post-treatment changes in glycemic variability using CGM, including mean amplitude of glycemic excursion (MAGE), peak post-prandial blood sugars, and glucose area under the curve.
Full Information
NCT ID
NCT01721382
First Posted
October 26, 2012
Last Updated
June 10, 2016
Sponsor
Nemours Children's Clinic
1. Study Identification
Unique Protocol Identification Number
NCT01721382
Brief Title
Treatment of Dysglycemia Using Sitagliptin in Adolescents With Cystic Fibrosis
Official Title
Treatment of Dysglycemia Using Sitagliptin in Adolescents With Cystic Fibrosis.
Study Type
Interventional
2. Study Status
Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
November 2012 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nemours Children's Clinic
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This pilot study will be conducted in adolescents with cystic fibrosis (CF) without diabetes but with abnormal glucose tolerance, and will assess the effects of sitagliptin on glucose regulation. An oral glucose tolerance test (OGTT) and a mixed meal tolerance test (MMTT), will be performed at baseline and again ~4 weeks after treatment with study drug. We will also look at blood sugars throughout the day using a continuous glucose monitor (CGM) before each time the MMTT/OGTT are performed. Several hormones that may affect the way the body regulates blood sugars will be measured in blood when the OGTT and MMTT are done. We will assess the effect this medicine has on blood sugars (using CGM) and the effect the medicine has on the hormones measured during the OGTT and MMTT.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis
Keywords
cystic fibrosis, CF, CFRD, sitagliptin, incretins, GLP1, GIP, beta cell function, adolescents
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
6 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sitagliptin
Arm Type
Experimental
Arm Description
Treatment with sitagliptin
Intervention Type
Drug
Intervention Name(s)
Sitagliptin
Primary Outcome Measure Information:
Title
Response to sitagliptin
Description
Baseline and stimulated C-peptide levels (using mixed meal tolerance test) before and after treatment with sitagliptin.
Time Frame
Change from baseline to ~4 weeks of study drug
Title
Response to sitagliptin
Description
Change in glycemic variability using continuous glucose monitoring data before and after treatment with dipeptidyl peptidase-4 inhibitor.
Time Frame
Change from baseline to ~4 weeks of study drug
Title
Response to sitagliptin
Description
Change in incretins concentrations (glucagon like peptide 1; glucose-dependent insulinotropic polypeptide) in response to study drug.
Time Frame
Change from baseline to ~4 weeks of study drug
Title
Response to sitagliptin
Description
Change in incretin (glucagon like peptide 1; glucose-dependent insulinotropic polypeptide) concentrations in response to study drug.
Time Frame
Change from baseline to ~4 weeks of study drug
Secondary Outcome Measure Information:
Title
Beta-cell function
Description
Beta-cell function will be measured using mixed meal tolerance tests (MMTT) and oral glucose tolerance tests (OGTT), assessing maximum concentration and area under the curve (AUC) of glucose, insulin and c-peptide for both OGTT and MMTT.
Time Frame
Change from baseline to ~4 weeks of study drug
Title
Continuous glucose monitoring (CGM)
Description
Baseline and post-treatment changes in glycemic variability using CGM, including mean amplitude of glycemic excursion (MAGE), peak post-prandial blood sugars, and glucose area under the curve.
Time Frame
change from baseline to ~4 weeks of study drug
10. Eligibility
Sex
All
Minimum Age & Unit of Time
13 Years
Maximum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with CF between 13 and <21 yrs old
Known impaired or indeterminate glucose tolerance (based on a prior OGTT)
No history of CFRD
Exclusion Criteria:
Insulin use in the last two months
Acute pulmonary exacerbation / oral corticosteroid use in the last 6 weeks
History of pancreatitis in the last 12 months
Skin rashes or conditions that may affect CGM placement and wear
Pregnancy or intent on becoming pregnant
Patients on growth hormone therapy
Renal insufficiency with creatinine clearance <50 ml/min (based on Schwartz formula)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Larry A Fox, MD
Organizational Affiliation
Nemours Children's Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nemours Children's Clinic
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Treatment of Dysglycemia Using Sitagliptin in Adolescents With Cystic Fibrosis
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