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Study of LYM-X-SORB™ to Improve Fatty Acid and Choline Status in Children With CF and PI

Primary Purpose

Cystic Fibrosis, Pancreatic Insufficiency

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Lym-X-Sorb powder
Placebo powder
Sponsored by
Avanti Polar Lipids, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cystic Fibrosis focused on measuring Cystic Fibrosis, Pancreatic Insufficiency, LYM-X-SORB™, LXS

Eligibility Criteria

6 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosed as having cystic fibrosis (CF) with pancreatic insufficiency (PI)
  • Subjects aged 6 to 17 years of age
  • In usual state of good health
  • Family and subject commitment to the 18-month study protocol
  • Fecal elastase < 15µg/g stool

Exclusion Criteria:

  • Forced expiratory volume at one second, % predicted (FEV1) < 40% predicted
  • Other chronic health conditions that may affect GI absorption, growth, dietary intake, nutritional status
  • Liver disease, lung transplant, celiac disease, allergy/intolerance to wheat/gluten, pregnant
  • Participation in another CF nutrition-related intervention study
  • Regular intake of fatty acids (i.e., fish oils) or choline nutritional supplements
  • Home parenteral lipid administration (i.e., intralipids)

Sites / Locations

  • Children's Hospital of Philadelphia (CHOP)

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

1

2

Arm Description

Outcomes

Primary Outcome Measures

Improvements in essential fatty acid (EFA) and choline status over a 12-month period.

Secondary Outcome Measures

Improvements in growth, nutritional, and pulmonary status over an 18-month period.

Full Information

First Posted
November 29, 2006
Last Updated
January 11, 2013
Sponsor
Avanti Polar Lipids, Inc.
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT00406536
Brief Title
Study of LYM-X-SORB™ to Improve Fatty Acid and Choline Status in Children With CF and PI
Official Title
Phase II Study: LYM-X-SORB™, an Organized Lipid Matrix: Fatty Acids and Choline in CF
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
January 2007 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
June 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Avanti Polar Lipids, Inc.
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

5. Study Description

Brief Summary
The purpose of this phase II research study is to evaluate the effectiveness of the next generation LYM-X-SORB™ in improving the essential fatty acid (EFA) and choline status for children and adolescents with Cystic Fibrosis (CF) and pancreatic insufficiency (PI).
Detailed Description
Fat malabsorption is common in individuals with cystic fibrosis (CF) and pancreatic insufficiency (PI). This places them at risk for caloric, essential fatty acid, and choline deficiency, which may in turn, lead to growth failure and a poorer clinical course. The purpose of this research study is to find whether or not taking LYM-X-SORB™ over an 18-month period, every day, will correct the problem people with CF and PI have with absorbing fat and choline. Participation will help CF doctors and other healthcare professionals learn more about the potential benefits of LYM-X-SORB™ to children and adolescents with CF and PI. These benefits may include better absorption of fat, better choline status, better growth in height, weight, muscle and bone, better lungs, and improvement of health status. The study will enroll a total of 78 participants from Children's Hospital of Philadelphia (CHOP) and from several other Cystic Fibrosis Centers. One half of the participants will be randomly picked to receive the active powder with the LYM-X-SORB™ supplement and one half will receive a placebo (with no active supplement).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis, Pancreatic Insufficiency
Keywords
Cystic Fibrosis, Pancreatic Insufficiency, LYM-X-SORB™, LXS

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
110 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Title
2
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Lym-X-Sorb powder
Intervention Description
Lym-X-Sorb is an organized matrix of lyso phosphatidylcholine (LPC), free fatty acid (FFA) and monoglyceride formulated at 20wt% with flour and sugar. A dosage contains 32 grams of powder and is consumed with food twice a day (6 to 11.9 years old) or three times per day (12 to 17.9 years old) for 18 months.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo powder
Intervention Description
The placebo is composed of soybean oil, sunflower oil, fully hydrogenated cottonseed oil and flax seed oil dispersed at 16wt% on flour and sugar. The placebo is >99% triglycerides with no trans fatty acids. The fatty acid composition and caloric content is designed to match the active supplement (Lym-X-Sorb). A dosage contains 32 grams of powder and is consumed with food twice a day (6 to 11.9 years old) or three times per day (12 to 17.9 years old) for 18 months.
Primary Outcome Measure Information:
Title
Improvements in essential fatty acid (EFA) and choline status over a 12-month period.
Time Frame
12-month period
Secondary Outcome Measure Information:
Title
Improvements in growth, nutritional, and pulmonary status over an 18-month period.
Time Frame
18-month period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed as having cystic fibrosis (CF) with pancreatic insufficiency (PI) Subjects aged 6 to 17 years of age In usual state of good health Family and subject commitment to the 18-month study protocol Fecal elastase < 15µg/g stool Exclusion Criteria: Forced expiratory volume at one second, % predicted (FEV1) < 40% predicted Other chronic health conditions that may affect GI absorption, growth, dietary intake, nutritional status Liver disease, lung transplant, celiac disease, allergy/intolerance to wheat/gluten, pregnant Participation in another CF nutrition-related intervention study Regular intake of fatty acids (i.e., fish oils) or choline nutritional supplements Home parenteral lipid administration (i.e., intralipids)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Walter A. Shaw, PhD
Organizational Affiliation
Avanti Polar Lipids, Inc.
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Virginia A. Stallings, MD
Organizational Affiliation
Children's Hospital of Philadelphia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital of Philadelphia (CHOP)
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

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Study of LYM-X-SORB™ to Improve Fatty Acid and Choline Status in Children With CF and PI

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