Study of the Nutritional, Metabolic, and Body Composition Profile in Children and Adolescents With Epidermolysis Bullosa
This study has been completed.
Sponsor:
Collaborator:
Baylor College of Medicine
Information provided by:
Office of Rare Diseases (ORD)
ClinicalTrials.gov Identifier:
NCT00004791
First received: February 24, 2000
Last updated: June 23, 2005
Last verified: December 2001
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
OBJECTIVES: I. Characterize the nutritional and metabolic profile of children and adolescents with epidermolysis bullosa.
II. Determine patterns of body composition in these patients. III. Determine the energy requirements of these patients by measuring resting energy expenditure.
IV. Assess protein nutrition by measuring lean body mass.
| Condition |
|---|
|
Epidermolysis Bullosa |
| Study Type: | Observational |
| Study Design: | Primary Purpose: Screening |
Resource links provided by NLM:
Genetics Home Reference related topics:
epidermolysis bullosa simplex
epidermolysis bullosa with pyloric atresia
junctional epidermolysis bullosa
U.S. FDA Resources
Further study details as provided by Office of Rare Diseases (ORD):
| Estimated Enrollment: | 15 |
| Study Start Date: | August 1995 |
PROTOCOL OUTLINE:
Data collected from a 5-day food diary are analyzed for protein, nutrient, and calorie intake. Nutritional, metabolic, and body composition are evaluated by indirect calorimetry, total body electrical conductivity, total body potassium, and lean body mass.
Eligibility| Ages Eligible for Study: | up to 18 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
PROTOCOL ENTRY CRITERIA:
- Epidermolysis bullosa
- Patient age: 2 months to 18 years
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00004791 History of Changes |
| Other Study ID Numbers: | 199/11912, BCM-H3246 |
| Study First Received: | February 24, 2000 |
| Last Updated: | June 23, 2005 |
| Health Authority: | United States: Federal Government |
Keywords provided by Office of Rare Diseases (ORD):
|
dermatologic disorders epidermolysis bullosa genetic diseases and dysmorphic syndromes rare disease |
Additional relevant MeSH terms:
|
Epidermolysis Bullosa Skin Abnormalities Congenital Abnormalities Skin Diseases, Genetic |
Genetic Diseases, Inborn Skin Diseases Skin Diseases, Vesiculobullous |
ClinicalTrials.gov processed this record on May 16, 2013