Title

Study of LYM-X-SORB™ to Improve Fatty Acid and Choline Status in Children With CF and PI
Phase II Study: LYM-X-SORB™, an Organized Lipid Matrix: Fatty Acids and Choline in CF
  • Phase

    Phase 2
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Intervention/Treatment

    lym-x-sorb ...
  • Study Participants

    110
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).
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).
Study Started
Jan 31
2007
Primary Completion
Jun 30
2012
Study Completion
Jun 30
2012
Last Update
Jan 14
2013
Estimate

Dietary Supplement Lym-X-Sorb powder

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.

Dietary Supplement Placebo powder

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.

1 Active Comparator

2 Placebo Comparator

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)
No Results Posted