Study on the Efficacy of Slow Release Insulin in Cystic Fibrosis Patients With Glucide Intolerance and Clinical Decay
Primary Purpose
Cystic Fibrosis, Glucose Intolerance
Status
Unknown status
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Insulin
Sponsored by
About this trial
This is an interventional treatment trial for Cystic Fibrosis focused on measuring Cystic Fibrosis, Glucose Intolerance
Eligibility Criteria
Inclusion Criteria:
- Ascertained diagnosis of CF
- Age ≥ 10 years
- Glucide intolerance: 2 pathologic OGTT ( at 120' glucose value: >140 mg% and <200 mg%) at 2-6 months' interval between each other
At least one of the following conditions:
- BMI (body mass index) < 10th centile for age and sex (according to Rolland Cachera 1991)
- Loss of one BMI centile class for age and sex in the last year (according to Rolland Cachera 1991)
- FEV1 ≤ 80% of predicted
- FEV1 decrease ≥ 10% in the last year
Exclusion Criteria:
- Specific contraindications for the use of glargine
Sites / Locations
- Pediatric Department, General Hospital,CF Center
- Ospedale Maggiore Policlinico, Adult CF Center
- Pediatric Department, Federico II University, Pediatric CF Center
- Pediatric Department G.De Cristina Hospital CF Center
- Bambino Gesù Hospital CF Center
- Policlinico Umberto I. CF Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
1
2
Arm Description
Insulin yes
Insulin no
Outcomes
Primary Outcome Measures
Nutritional status evaluated as variations of Z score of BMI
Secondary Outcome Measures
Glucose tolerance improvement evaluated as improvement of glycometabolic parameter (glycosylated Hb)
Full Information
NCT ID
NCT00687466
First Posted
May 27, 2008
Last Updated
August 3, 2009
Sponsor
Fondazione per la ricerca sulla Fibrosi Cistica
1. Study Identification
Unique Protocol Identification Number
NCT00687466
Brief Title
Study on the Efficacy of Slow Release Insulin in Cystic Fibrosis Patients With Glucide Intolerance and Clinical Decay
Official Title
Phase 3 Study on the Efficacy of Slow Release Insulin in Cystic Fibrosis Patients With Glucide Intolerance and Clinical Decay
Study Type
Interventional
2. Study Status
Record Verification Date
August 2009
Overall Recruitment Status
Unknown status
Study Start Date
August 2005 (undefined)
Primary Completion Date
October 2009 (Anticipated)
Study Completion Date
October 2009 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Fondazione per la ricerca sulla Fibrosi Cistica
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to evaluate whether the anticipated use of glargine in CF patients with glucose intolerance may prevent the worsening of nutritional status and pulmonary function.
Detailed Description
Diabetes mellitus may often complicate the cystic fibrosis course, and it is usually preceded by a condition defined as glucose intolerance, during which a significant decay of patient's general conditions is observed. A slow release insulin (glargine) has become available in the market for diabetic patients: its characteristics allow for a single daily dose, and no need of repeated daily monitoring of glycemia.
In this randomized controlled clinical trial we evaluate whether the anticipated use of glargine in CF patients with glucose intolerance may prevent the worsening of nutritional status and pulmonary function.
Eligible patients who will accept to participate to this study will be randomly allocated in the group who will or will not receive glargine as additional supportive therapy. Patients will in any case continue the CF therapy prescribed by their treating physicians and their usual diet. All the patients will be evaluated every three months to assess their nutritional, pulmonary and glycometabolic status. The follow-up will continue until the 18th month after the study entry.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis, Glucose Intolerance
Keywords
Cystic Fibrosis, Glucose Intolerance
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
70 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Insulin yes
Arm Title
2
Arm Type
No Intervention
Arm Description
Insulin no
Intervention Type
Drug
Intervention Name(s)
Insulin
Other Intervention Name(s)
Lantus
Intervention Description
Insulin Glargine will be administered subcutaneously at the dosage of 0.1 U/Kg/die for three months. In case no hypoglycemic episodes occur during this period, the dosage will be increased to 0.15 U/Kg/die in occasion of the first control (T1) and will be scheduled for other three months. If even during this latter period no cases no hypoglycemic episodes occur, at the second control (T2) the dosage will be increased to the maximum of 0.2/U/Kg/die. It is generally accepted that the final dosage of glargine can be tailored to each patient, but it should be maintained between 0.1 and 0.2 U/Kg/die.
Glargine should be administered once daily in the morning and always at the same hour.
Primary Outcome Measure Information:
Title
Nutritional status evaluated as variations of Z score of BMI
Time Frame
At recruitment time and at +3, +6, +9, +12, +15, +18 months
Secondary Outcome Measure Information:
Title
Glucose tolerance improvement evaluated as improvement of glycometabolic parameter (glycosylated Hb)
Time Frame
At time recruitment and +3,+6,+9+12+15+18 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Ascertained diagnosis of CF
Age ≥ 10 years
Glucide intolerance: 2 pathologic OGTT ( at 120' glucose value: >140 mg% and <200 mg%) at 2-6 months' interval between each other
At least one of the following conditions:
BMI (body mass index) < 10th centile for age and sex (according to Rolland Cachera 1991)
Loss of one BMI centile class for age and sex in the last year (according to Rolland Cachera 1991)
FEV1 ≤ 80% of predicted
FEV1 decrease ≥ 10% in the last year
Exclusion Criteria:
Specific contraindications for the use of glargine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Laura Minicucci, MD
Organizational Affiliation
G.Gaslini Institute Pediatric Department CF Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pediatric Department, General Hospital,CF Center
City
Cerignola (Foggia)
Country
Italy
Facility Name
Ospedale Maggiore Policlinico, Adult CF Center
City
Milano
Country
Italy
Facility Name
Pediatric Department, Federico II University, Pediatric CF Center
City
Napoli
Country
Italy
Facility Name
Pediatric Department G.De Cristina Hospital CF Center
City
Palermo
Country
Italy
Facility Name
Bambino Gesù Hospital CF Center
City
Roma
Country
Italy
Facility Name
Policlinico Umberto I. CF Center
City
Roma
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
10499886
Citation
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Results Reference
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Citation
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Citation
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Results Reference
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Citation
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Citation
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Citation
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Study on the Efficacy of Slow Release Insulin in Cystic Fibrosis Patients With Glucide Intolerance and Clinical Decay
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