Safety and Efficacy of an Antioxidant-rich Multivitamin Supplement in Cystic Fibrosis
Primary Purpose
Cystic Fibrosis
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
AquADEK
Sponsored by
About this trial
This is an interventional treatment trial for Cystic Fibrosis focused on measuring cystic fibrosis, vitamins, antioxidants, anthropometric measurements, pulmonary function
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of CF as evidenced by a sweat chloride test > 60mEq/L or by the presence of two known CF mutations
- Male or female, ages between 10-40 years old
- > 30 kg body weight
- FEV1 > 35% predicted for age and height
- Clinically stable with no recent hospitalization within the past 2 weeks
Exclusion Criteria:
- Significant liver disease as defined by clinical findings of portal hypertension or cirrhosis or AST, ALT, or GGT >2x upper limits of normal within the previous 6 months
- Poor compliance with medical regimen as assessed by CF clinic care providers
- Oral supplementation with AquADEKs or another source of beta-carotene or CoQ10 in the 2 months prior to the study
- Pregnant or lactating
- Participation in another interventional clinical trial within the previous 2 weeks
- Difficulty swallowing softgels
Sites / Locations
- The Children's Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Antioxidant-enriched multivitamin supplement
Arm Description
Outcomes
Primary Outcome Measures
Plasma levels of beta-carotene
Secondary Outcome Measures
Plasma levels of coenzyme Q10, retinol (Vitamin A), 25-hydroxy vitamin D, alpha- and gamma-tocopherols (Vitamin E), PIVKA-II
Full Information
NCT ID
NCT01018303
First Posted
November 19, 2009
Last Updated
October 11, 2012
Sponsor
University of Colorado, Denver
Collaborators
Cystic Fibrosis Foundation, Yasoo Health, National Institutes of Health (NIH)
1. Study Identification
Unique Protocol Identification Number
NCT01018303
Brief Title
Safety and Efficacy of an Antioxidant-rich Multivitamin Supplement in Cystic Fibrosis
Official Title
Safety and Efficacy of a Novel Antioxidant-rich Multivitamin Supplement for Persons With Cystic Fibrosis
Study Type
Interventional
2. Study Status
Record Verification Date
October 2012
Overall Recruitment Status
Completed
Study Start Date
August 2007 (undefined)
Primary Completion Date
June 2008 (Actual)
Study Completion Date
November 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Colorado, Denver
Collaborators
Cystic Fibrosis Foundation, Yasoo Health, National Institutes of Health (NIH)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to test the safety and efficacy of the final commercial formulation of an antioxidant enriched multivitamin supplement in softgel capsule form (AquADEKs) in increasing the plasma levels of certain nutrients and antioxidants in individuals with cystic fibrosis.
Hypothesis: An oral antioxidant-rich multivitamin supplement (AquADEKs), which uses a Generally Regarded As Safe (GRAS) molecule to form micelle-like vehicles, will safely increase systemic levels of beta-carotene, coenzyme Q10, and gamma-tocopherol, decrease PIVKA-II levels, while maintaining levels of vitamins A and D in the normal range in persons with CF > 10 years of age.
Detailed Description
In cystic fibrosis (CF), pancreatic insufficiency and a diminished bile acid pool cause malabsorption of important nutrients and dietary components leading to poor nutritional status and oxidative stress. Of particular significance is the malabsorption of fat-soluble nutrients, such as vitamins A, D, E and K which are critical for normal metabolic functions. Furthermore this malabsorption prevents individuals with CF from adequately absorbing and maintaining levels of lipophilic nutrients and antioxidants such as beta-carotene, coenzyme Q10 (CoQ10) and gamma-tocopherol which may provide benefits when supplied at levels higher than those obtained from normal diets. Current standard of care supplementation often does not normalize the blood levels of certain vitamins and antioxidants.
An oral formulation, which can form micelle-like vehicles, can be used to overcome the malabsorption of these nutrients in CF patients. A pilot study of a prototype formulation showed both safety and efficacy in increasing systemic levels of target nutrients. This study will test the safety and efficacy of the final commercial formulation (AquADEKs) in the form of a softgel capsule in increasing the plasma levels of certain nutrients and antioxidants.
Hypothesis: An oral antioxidant-rich multivitamin supplement (AquADEKs), which uses a Generally Regarded As Safe (GRAS) molecule to form micelle-like vehicles, will safely increase systemic levels of beta-carotene, coenzyme Q10, and gamma-tocopherol, decrease PIVKA-II levels, while maintaining levels of vitamins A and D in the normal range in persons with CF > 10 years of age.
Specific Aims:
To evaluate the safety of AquADEKs by monitoring patient reported symptoms and adverse events, and following vitamin and antioxidant levels, particularly vitamin A, to ensure that they do not exceed normative ranges after supplementation.
To determine the efficacy of AquADEKs in increasing the antioxidants beta-carotene, CoQ10, and γ-tocopherol and maintaining plasma levels of vitamins A, D, α-tocopherol and PIVKA-II (surrogate of vitamin K status) in the normal range.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis
Keywords
cystic fibrosis, vitamins, antioxidants, anthropometric measurements, pulmonary function
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
17 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Antioxidant-enriched multivitamin supplement
Arm Type
Experimental
Intervention Type
Dietary Supplement
Intervention Name(s)
AquADEK
Intervention Description
Two AquADEK softgel vitamins on a daily basis x 12 weeks
Primary Outcome Measure Information:
Title
Plasma levels of beta-carotene
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Plasma levels of coenzyme Q10, retinol (Vitamin A), 25-hydroxy vitamin D, alpha- and gamma-tocopherols (Vitamin E), PIVKA-II
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of CF as evidenced by a sweat chloride test > 60mEq/L or by the presence of two known CF mutations
Male or female, ages between 10-40 years old
> 30 kg body weight
FEV1 > 35% predicted for age and height
Clinically stable with no recent hospitalization within the past 2 weeks
Exclusion Criteria:
Significant liver disease as defined by clinical findings of portal hypertension or cirrhosis or AST, ALT, or GGT >2x upper limits of normal within the previous 6 months
Poor compliance with medical regimen as assessed by CF clinic care providers
Oral supplementation with AquADEKs or another source of beta-carotene or CoQ10 in the 2 months prior to the study
Pregnant or lactating
Participation in another interventional clinical trial within the previous 2 weeks
Difficulty swallowing softgels
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Scott D Sagel, MD
Organizational Affiliation
University of Colorado, Denver
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Children's Hospital
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
20961818
Citation
Sagel SD, Sontag MK, Anthony MM, Emmett P, Papas KA. Effect of an antioxidant-rich multivitamin supplement in cystic fibrosis. J Cyst Fibros. 2011 Jan;10(1):31-6. doi: 10.1016/j.jcf.2010.09.005. Epub 2010 Oct 20.
Results Reference
result
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Safety and Efficacy of an Antioxidant-rich Multivitamin Supplement in Cystic Fibrosis
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