Walking Program in Fatty Liver Children With Phenylketonuria
- Conditions
- PhenylketonuriasNon Alcoholic Fatty Liver
- Registration Number
- NCT06718842
- Lead Sponsor
- Cairo University
- Brief Summary
phenylketonuria (commonly known as PKU) is an inherited disorder that increases the levels of a substance called phenylalanine in the blood. PKU is usually associated with many metabolic complication including non-alcoholic fatty liver
- Detailed Description
this study will include PKU children sufferers 9n=40) with non-alcoholic fatty liver to be randomly assigned to group I (n=20) that will perform walking program (online supervised free walking that will be applied daily for eight weeks) or group II (N=20) that will act as waitlisted children
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 40
- PKU children
- obese children
- fatty liver children (non-alcoholic fatty liver)
- cardiac children
- diabetic children
- neurogenic disorders
- respiratory and renal problems
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method alanine transamianse it will be assessed after eight weeks it is a serum liver enzyme
- Secondary Outcome Measures
Name Time Method aspartate tranaminase it will be assessed after eight weeks it is a serum liver enzyme
Gamma-glutamyl Transferase it will be assessed after eight weeks it is a serum liver enzyme
alkaline phosphatase it will be assessed after eight weeks it is a serum liver enzyme
triglycerides it will be assessed after eight weeks it will be measured in the serum
body mass index it will be assessed after eight weeks it will be measured after emptying bladder
Related Research Topics
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Trial Locations
- Locations (1)
Cairo University
🇪🇬Dokki, Giza, Egypt