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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00406536
Other study ID # DK60302
Secondary ID R44DK0603022R44D
Status Completed
Phase Phase 2
First received November 29, 2006
Last updated January 11, 2013
Start date January 2007
Est. completion date June 2012

Study information

Verified date January 2013
Source Avanti Polar Lipids, Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Federal GovernmentUnited States: Institutional Review Board
Study type Interventional

Clinical Trial 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).


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).


Recruitment information / eligibility

Status Completed
Enrollment 110
Est. completion date June 2012
Est. primary completion date June 2012
Accepts healthy volunteers No
Gender Both
Age group 6 Years to 17 Years
Eligibility 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)

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

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.
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.

Locations

Country Name City State
United States Children's Hospital of Philadelphia (CHOP) Philadelphia Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
Avanti Polar Lipids, Inc. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

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* Note: There are 158 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary Improvements in essential fatty acid (EFA) and choline status over a 12-month period. 12-month period No
Secondary Improvements in growth, nutritional, and pulmonary status over an 18-month period. 18-month period No
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