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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02555579
Other study ID # 0451-15-EP
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 26, 2015
Est. completion date September 20, 2017

Study information

Verified date September 2023
Source University of Nebraska
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a study to determine if a simplified protein counting system, including the free usage of fruits and vegetables low in phenylalanine, will improve the metabolic control in teens and adults with phenylketonuria (PKU). Anybody with a positive diagnosis of PKU, between the ages of 13-65 years will be invited to participate in this study. Subjects will be educated on the simplified system upon enrollment, and historical phenylalanine (Phe) levels will be used for comparison. Subjects will also be asked about their attitudes towards their current Phe counting system.


Description:

This is a study to determine if a simplified protein counting system, including the free usage of fruits and vegetables low in phenylalanine, will improve the metabolic control in teens and adults with phenylketonuria (PKU). Anybody with a positive diagnosis of PKU, between the ages of 13-65 years will be invited to participate in this study. Subjects will be educated on the simplified system upon enrollment, and historical phenylalanine (Phe) levels will be used for comparison. Subjects will also be asked about their attitudes towards their current Phe counting system. Upon enrollment, a 3-day food record and Phe levels over the past 12 months will be collected. Demographic information will be asked, as well as questions regarding their current Phe counting system. Patients will be educated on the new counting system, stressing 3 key principles: 1) free use of fruits and vegetables, low in protein, 2) protein counting as a simpler version of Phe counting, including reinforcement of label reading, and 3) daily use of PKU formula for enhanced nutrient and protein intake. Patients will be given written educational tools to reinforce this new method. At the end of the 12 months, subjects will be asked to provide a 3-day food record, and questions will be asked about their attitudes toward the use of the new simplified system. Phenylalanine levels from the 12-month study period will be used to compare with historical data.


Recruitment information / eligibility

Status Completed
Enrollment 33
Est. completion date September 20, 2017
Est. primary completion date September 20, 2017
Accepts healthy volunteers No
Gender All
Age group 13 Years to 65 Years
Eligibility Inclusion Criteria: 1. Positive diagnosis of PKU 2. Males and females >13 year of age 3. Currently on phenylalanine-restricted diet Exclusion Criteria: 1. Any woman planning, or becoming pregnant during study duration 2. Any patient who starts Kuvan during the study, as Kuvan lowers phenylalanine levels in some patients. 3. Any patient currently enrolled in other research studies (Prism 301/302 Protocol; Institutional Review Board Protocol # 376-13-FB)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Dietary Protein Counting and Free Fruits and Vegetables
Subjects will be educated on new simplified diet approach and phenylalanine levels will be monitored for 1 year, and will be compared to 12 months prior to study enrollment

Locations

Country Name City State
United States Children's Hospital & Medical Center Omaha Nebraska
United States Monroe-Meyer Insititute Omaha Nebraska
United States Nebraska Medicine, Midtown Health Center Omaha Nebraska
United States Unversity of Nebraska Medical Center Omaha Nebraska

Sponsors (1)

Lead Sponsor Collaborator
University of Nebraska

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Metabolic Control in Teens and Adults with PKU phenylalanine levels 12 months
Secondary attitudes towards simplified diet approach qualitative data collection 12 months
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