search
Back to results

Cystic Fibrosis (CF) Exacerbation and Insulin Treatment

Primary Purpose

Cystic Fibrosis, Impaired Glucose Tolerance, Pulmonary Exacerbation

Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
novorapid / humalog short acting insulin
Novo Rapid Insulin (Novonordisk)
Sponsored by
Hadassah Medical Organization
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cystic Fibrosis focused on measuring Normal Glucose Tolerance Test, Mixed Meal Tolerance Test, Cystic Fibrosis, Pulmonary Exacerbation, Impaired Glucose Tolerance Test, Insulin Therapy

Eligibility Criteria

10 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Confirmed diagnosis of CF according to standard criteria
  • Pancreatic insufficiency
  • Age > 10 years
  • Normal oral glucose tolerance test (OGTT) in the past 12 month.
  • Acute pulmonary exacerbation (PE) according to the treating physician requires treatment with intravenous antibiotics

Exclusion Criteria:

  • CF-related diabetes/impaired glucose tolerance test (IGTT) in a mixed meal tolerance test performed during full remission from pulmonary exacerbation

Sites / Locations

  • Hadassah Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

insulin

Arm Description

patients who will get insulin with main meals during Intravenous (IV) antibiotic therapy due to pulmonary exacerbation

Outcomes

Primary Outcome Measures

delta Forced Expiratory Volume in 1 second (FEV1%) predicted
change in lung function parameter %FEV1 predected from baseline before the exacerbatio to day 0, the day of hospitalization due to the pulmonary exacerbation and to day 14, after 2 weeks of Intra Venous (IV)Antibiotic therapy, due to Pulmonary Exacerbation (PE).

Secondary Outcome Measures

change in Body Mass Index (BMI)
weight and hight will be measured on arrival to hospital (day 0)of the pulmonary exacerbation and again on day 14 of the pulmonary exacerbation and. BMI will be calculated and compared to BMI perior to the exacerbation

Full Information

First Posted
June 9, 2010
Last Updated
June 22, 2010
Sponsor
Hadassah Medical Organization
search

1. Study Identification

Unique Protocol Identification Number
NCT01149005
Brief Title
Cystic Fibrosis (CF) Exacerbation and Insulin Treatment
Official Title
Evaluation of Glucose Tolerance and Insulin Treatment in Non Diabetic Patients With Cystic Fibrosis During Acute Pulmonary Exacerbation
Study Type
Interventional

2. Study Status

Record Verification Date
June 2010
Overall Recruitment Status
Unknown status
Study Start Date
June 2010 (undefined)
Primary Completion Date
June 2015 (Anticipated)
Study Completion Date
December 2015 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Hadassah Medical Organization

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to evaluate whether insulin treatment during pulmonary exacerbation (PE) in patients with Cystic Fibrosis (CF)and normoglycemia improves their short term outcome by normalizing the glycemic profile and enhancing recovery. the investigators would like to evaluate whether insulin treatment during exacerbation improves both the general clinical condition of these patients and also has a protecting effect on ß-cells by preventing the deleterious effect of "chronic" hyperglycemia.
Detailed Description
The life expectancy of patients with cystic fibrosis (CF) has increased over the last decades due to improved understanding of the disease and new treatments. CF patients who live longer develop glucose intolerance and cystic fibrosis related diabetes (CFRD), in fact, routine annual screening by Oral Glucose Tolerance Tests (OGTT) shows that the prevalence of CFRD increases with age. CFRD is primarily an insulinopenic condition characterized by an impaired and delayed insulin secretion, as a consequence of fibrosis in the exocrine pancreatic tissue that compromises the ß-cell function. The occurrence of CFRD is significantly related to increased morbidity and mortality. Based on data from the CF Patients Registry in the USA, the mortality rate of patients with CFRD is six-fold higher than that of patients without CFRD. Our pilot study proved that during pulmonary exacerbation (PE), CF patients with Normal Glucose Tolerance (NGT) exhibited early latent diabetic glucose intolerance in Oral Glucose Tolerance Test(OGTT) which becomes completely normalized 3-4 weeks after resolution of PE. These patients who are considered to be normoglycemic may experience relatively long periods of hyperglycemia during recurrent events of pulmonary infections. Chronically increased glucose values during PE have an adverse impact on pulmonary function both during PE and in the long-term. Hyperglycemia may increase the duration and extent of recovery from PE. Furthermore it may impair the ability to overcome lung infections by directly stimulating the growth of respiratory pathogens. Finally, hyperglycemia per-se during stressful conditions may worsen the general outcome. Insulin therapy is considered routine treatment for patients with CFRD. In addition to normalizing glucose levels, insulin has a beneficial effect on general pulmonary function and nutritional status, possibly due to its anabolic effect. No routine or formal guidelines for treating PE hyperglycemia are currently available. Normal Glucose Tolerance (NGT)patients, who are hyperglycemic during PE only, are generally not intensively treated for this condition, except if the treating physician decides on interventional insulin treatment. Some patients may experience relatively long periods of hyperglycemia during recurrent events of pulmonary infections.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis, Impaired Glucose Tolerance, Pulmonary Exacerbation
Keywords
Normal Glucose Tolerance Test, Mixed Meal Tolerance Test, Cystic Fibrosis, Pulmonary Exacerbation, Impaired Glucose Tolerance Test, Insulin Therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
insulin
Arm Type
Experimental
Arm Description
patients who will get insulin with main meals during Intravenous (IV) antibiotic therapy due to pulmonary exacerbation
Intervention Type
Drug
Intervention Name(s)
novorapid / humalog short acting insulin
Other Intervention Name(s)
Humalog insulin
Intervention Description
1-4 units will be injected Subcutaneously (SC), before every main meal.
Intervention Type
Drug
Intervention Name(s)
Novo Rapid Insulin (Novonordisk)
Other Intervention Name(s)
Humalog insulin lispro
Intervention Description
Novo Rapid Insulin (Novonordisk) will be administered before each main meal 1-4 units depends on the patients weight
Primary Outcome Measure Information:
Title
delta Forced Expiratory Volume in 1 second (FEV1%) predicted
Description
change in lung function parameter %FEV1 predected from baseline before the exacerbatio to day 0, the day of hospitalization due to the pulmonary exacerbation and to day 14, after 2 weeks of Intra Venous (IV)Antibiotic therapy, due to Pulmonary Exacerbation (PE).
Time Frame
day 0 of the pulmonary exacerbation, to day 14 of the pulmonary exacerbation
Secondary Outcome Measure Information:
Title
change in Body Mass Index (BMI)
Description
weight and hight will be measured on arrival to hospital (day 0)of the pulmonary exacerbation and again on day 14 of the pulmonary exacerbation and. BMI will be calculated and compared to BMI perior to the exacerbation
Time Frame
baseline BMI will be compared with BMI on day 0- the day of hospitalization due to the pulmonary exacerbation, and to day 14, after 2 weeks of Intra Venous (IV)Antibiotic therapy, due to Pulmonary Exacerbation (PE).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed diagnosis of CF according to standard criteria Pancreatic insufficiency Age > 10 years Normal oral glucose tolerance test (OGTT) in the past 12 month. Acute pulmonary exacerbation (PE) according to the treating physician requires treatment with intravenous antibiotics Exclusion Criteria: CF-related diabetes/impaired glucose tolerance test (IGTT) in a mixed meal tolerance test performed during full remission from pulmonary exacerbation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David H Zangen, Dr.
Organizational Affiliation
Hadassah Medical Organization
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hadassah Hospital
City
Jerusalem
Country
Israel
Facility Contact:
First Name & Middle Initial & Last Name & Degree
David H Zangen, Dr.
Phone
97225844111
Ext
74488
Email
ZangenD@hadassah.org.il
First Name & Middle Initial & Last Name & Degree
Hila Elyashar-Earon, RD
Email
hilae@hadassah.org.il
First Name & Middle Initial & Last Name & Degree
David H Zangen, Dr.

12. IPD Sharing Statement

Citations:
PubMed Identifier
20188638
Citation
Sc NN, Shoseyov D, Kerem E, Zangen DH. Patients with cystic fibrosis and normoglycemia exhibit diabetic glucose tolerance during pulmonary exacerbation. J Cyst Fibros. 2010 May;9(3):199-204. doi: 10.1016/j.jcf.2010.02.001. Epub 2010 Feb 25.
Results Reference
background

Learn more about this trial

Cystic Fibrosis (CF) Exacerbation and Insulin Treatment

We'll reach out to this number within 24 hrs