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Phenylalanine-free Diet for Patients With Secondary Hyperphenylalaninemia in ICU

Primary Purpose

Non-Phenylketonuric Hyperphenylalaninemia

Status
Recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Phenylalanine-free milk
Sponsored by
Chang Gung Memorial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non-Phenylketonuric Hyperphenylalaninemia focused on measuring phenylalanine, intensive care unit, nutritional intervention

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. at critical status with APACHE II score >15 (with or without using ventilator);
  2. with the need of staying in ICU >48 hours;
  3. fasting plasma phenylalanine concentration >112 uM; and
  4. age >20 years old

Exclusion Criteria:

  1. comorbid disorders other than the main cause for ICU admission that might also compromise survival within three months, such as cancer at terminal status;
  2. expected life span< 3 days; and
  3. undergoing hemodialysis.

Sites / Locations

  • Chang Gung Memorial HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

phenylalanine-free diet

Arm Description

phenylalanine-free diet for patients with hyperphenylalaninemia

Outcomes

Primary Outcome Measures

fasting plasma phenylalanine concentration
fasting plasma phenylalanine concentration <112 uM

Secondary Outcome Measures

Full Information

First Posted
April 26, 2021
Last Updated
July 14, 2023
Sponsor
Chang Gung Memorial Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04896281
Brief Title
Phenylalanine-free Diet for Patients With Secondary Hyperphenylalaninemia in ICU
Official Title
Phenylalanine-free Diet Lowers the Blood Phenylalanine Levels in Patients With High Phenylalanine Level in the Intensive Care Unit
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 30, 2021 (Actual)
Primary Completion Date
February 28, 2024 (Anticipated)
Study Completion Date
February 28, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chang Gung Memorial Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Hyperphenylalaninemia is not only present in patients with congenital phenylketonuria. In adults with critical illness, hyperphenylalaninemia is noted in some patients and is associated with high mortality rate. Hyperphenylalaninemia can cause metabolic acidosis, brain dysfunction, and metabolic disturbance. We would like to see whether the phenylalanine-free milk for congenital phenylketonuria is also effective in lowering the blood phenylalanine concentrations in patients with critical illness in ICU and hyperphenylalaninemia.
Detailed Description
Background: Patients in the intensive care unit often suffer from problems such as high metabolic rate and high tissue breakdown rate under the severe stress of critical diseases. Phenylalanine is an amino acid in the human body and is rich in muscle tissue. However, current studies have found that if the concentration of phenylalanine in the blood is abnormally increased, it may indicate that the tissue is decomposing in large quantities. This phenomenon may be related to disease severity. Our recent observational study of patients in the intensive care unit found that patients with elevated blood phenylalanine had a four-fold increase in mortality within one year. The most common cause of phenylalanine concentration elevation in the blood is a rare disease that occurs in infants with congenital metabolic abnormalities, called congenital phenylketonuria (PKU). The abnormally elevated phenylalanine concentration can lead to toxicity and cause brain hypoplasia, mental retardation, consciousness disturbance, and even seizure. These PKU patients must be treated with milk diet that contains low amount of phenylalanine in order to lower the phenylalanine concentrations. At present, in medicine, although there have been clear medical care strategy for infants with congenital PKU, there is still no clear medical care strategy for adult patients. Research purpose: To investigate whether patients with high blood phenylalanine concentration in the intensive care unit can reduce the blood phenylalanine concentration by a diet without phenylalanine, so as to develop personalized high-quality and specific treatments. Methods: We aim to have complete study in 30 patients (based on our previous study, to recruit 30 patients with high phenylalanine, we need 100 ICU patients for screening) Intervention protocol Phenylalanine-free milk will be fed for 3 days after enrollment. The milk is purchased from ABBOTT company. The content of the whole nutrition for a daily need is also personalized based on the calculation by our dieticians. After the completion of the study, diet will be back to normal diet for all patients. Study end points: the 3-day study period completed Blood sampling and examination for Phenylalanine measurement (DBS) Fasting phenylalanine level will be measured by LC/MS-MS using the dry blood spot method (blood sample is collected by finger sting) in all included patients in the next morning after informed consent signed. Blood applied on filter cards is dried for at least 3 h at room temperature. DBS cards are stored at room temperature for 0-6 days prior to analyses. Phenylalanine concentrations in DBS are measured with LC-MS/MS, using a calibration curve in 0.1 N HCl. The report will be received one day after dry blood spot collected. Once the result of measurement shows the concentration of phenylalanine >112 uM, this patient is enrolled for formal study. All enrolled patients will take the measurement of phenylalanine levels by dry blood spot every 12 hours for the following 4 days until study protocol finished. Phenylalanine measurement by UPLC: In the meanwhile, fasting blood will be collected by venipuncture in EDTA-containing tubes on the morning of screening, 2 and 4 days after diet intervention. The collected blood will be used to measure phenylalanine level by UPLC (ultra-performance liquid chromatography). Plasma samples (100μL) are precipitated with 10% sulfosalicylic acid. After protein precipitation and centrifugation, derivatization is initiated by AQC in acetonitrile. Amino acids are then analyzed using the ACQUITY UPLC System, consisting of a Binary Solvent Manager, a Sample Manager, and a Tunable UV detector. We use EmpowerTM 2 Software to control the system and collect data. Separations are performed on a 2.1×100mm ACQUITY BEH C18 column at a flow rate of 0.70mL/min. The average intra-assay coefficient of variation is 2.6% for phenylalanine. The total coefficient of variation is 2.7% for phenylalanine. The detection limit is 3.3μM for phenylalanine. The linear range is 25-500 μM. APACHE II scores Disease severity is evaluated by calculating APACHE II score on the first day of ICU admission.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-Phenylketonuric Hyperphenylalaninemia
Keywords
phenylalanine, intensive care unit, nutritional intervention

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
phenylalanine-free diet
Arm Type
Experimental
Arm Description
phenylalanine-free diet for patients with hyperphenylalaninemia
Intervention Type
Dietary Supplement
Intervention Name(s)
Phenylalanine-free milk
Intervention Description
Intervention protocol Phenylalanine-free milk will be fed for 3 days after enrollment. The milk is purchased from ABBOTT company. The content of the whole nutrition for a daily need is also personalized based on the calculation by our dieticians. After the completion of the study, diet will be back to normal diet for all patients.
Primary Outcome Measure Information:
Title
fasting plasma phenylalanine concentration
Description
fasting plasma phenylalanine concentration <112 uM
Time Frame
the 3-day study period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: at critical status with APACHE II score >15 (with or without using ventilator); with the need of staying in ICU >48 hours; fasting plasma phenylalanine concentration >112 uM; and age >20 years old Exclusion Criteria: comorbid disorders other than the main cause for ICU admission that might also compromise survival within three months, such as cancer at terminal status; expected life span< 3 days; and undergoing hemodialysis.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
CHAO-HUNG WANG, MD, PhD
Phone
0224313131
Ext
2923
Email
bearty@cgmh.org.tw
First Name & Middle Initial & Last Name or Official Title & Degree
Min-Hui LIU, RN, PhD
Phone
0224313131
Ext
2245
Email
min4108@cgmh.org.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
CHAO-HUNG WABG, MD, PhD
Organizational Affiliation
CHANG GUNG MEMORIAL HOSPITAL, KEELUNG
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chang Gung Memorial Hospital
City
Keelung
ZIP/Postal Code
402
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
CHAO-HUNG WANG, MD
Phone
+886-2-24313131
Ext
2923
Email
bearty54@gmail.com
First Name & Middle Initial & Last Name & Degree
CHAO-HUNG WANG, MD

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
undecided

Learn more about this trial

Phenylalanine-free Diet for Patients With Secondary Hyperphenylalaninemia in ICU

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