Simple Breath Test to Examine Phenylalanine Metabolism

NCT ID: NCT02009904

Last Updated: 2020-09-24

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 20 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2013-01-31
• Study Completion Date: 2016-09-30

Brief Summary

Phenylketonuria(PKU)is a rare condition caused by the body's inability to properly breakdown an amino acid called phenylalanine(PHE), due to a missing enzyme, phenylalanine hydroxylase(PAH). When the enzyme is missing and/or not functioning properly, it increases the level of PHE in the body. High levels of PHE can cause severe brain damage or nerve damage unless the children are on a strict low PHE diet. A low PHE diet restricts the intake of protein rich foods and can pose a significant burden to both the patient and the family.

Investigators at the University of British Columbia and British Columbia Children's Hospital will examine the phenylalanine metabolism in children with PKU using a simple breath test.

Patients (5-18y) receiving standard clinical care at the BC Children's Hospital's Biochemical Diseases Clinic will be enrolled.The study will be conducted twice on each patient. Baseline measurements will be performed at the beginning of each study for each patient.The Physician in charge will then prescribe the standard dose of sapropterin dihydrochloride (Kuvan®) (20mg/kg/d) or otherwise as deemed appropriate by the physician-in-charge. The test will be repeated a week (minimum) after the beginning of treatment with the prescribed dose.

The investigators propose that children who are responsive to sapropterin dihydrochloride (Kuvan®) will have increased 13CO2 in breath after treatment, and those who do not respond will have no change in the 13CO2 in the breath before and after treatment.

As a comparison to the experimental group, age and gender matched healthy controls will also be studied. The test in healthy controls will be performed once without any intervention, and is only used as a comparative value.

Conditions

Phenylketonuria (PKU)

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Study Groups

Phenylketonuria (PKU); Healthy Controls

Children with PKU (5-18y); Age and Gender matched healthy subjects for comparison

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

Study Subjects:

1. Children (4-18y)diagnosed with PKU

2. Parent(s) or guardian(s) willing and able to provide informed signed consent.

3. Parent(s) or guardian(s) willing and able to comply with all study procedures

Healthy controls:

1. Healthy Children (4-18y) with no health condition

2. Willing to go through an initial screening for age and gender match

3. Parents or guardians willing and able to provide informed signed consent.

4. Parents or guardians willing and able to comply with study procedures

Exclusion Criteria

Study Subjects:

1. Children < 4y of age diagnosed with PKU, as it may be challenging to collect breath samples and perform indirect calorimeter in very young children

2. Children (4-18y)who are diagnosed with PKU, but are currently ill, with a fever, cold, vomiting or diarrhea

Healthy controls:

1. Healthy Children < 4y of age , as it may be challenging to collect breath samples and perform indirect calorimeter in very young children.

2. Healthy Children (4-18y), but are currently ill, with a fever, cold, vomiting or diarrhea.

• Minimum Eligible Age: 5 Years
• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Rare Disease Foundation, Vancouver, Canada

OTHER

Sponsor Role: collaborator

University of British Columbia

OTHER

Sponsor Role: lead

Responsible Party

Rajavel Elango, PhD

Principle Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Rajavel Elango, Ph.D

Role: PRINCIPAL_INVESTIGATOR

University of British Columbia

Locations

Child & Family Research Institute

Vancouver, British Columbia, Canada

Countries

Canada

Other Identifiers

H12-01421

Identifier Type: -

Identifier Source: org_study_id