This study is phase 2 open-label, single-arm, multi-center clinical trial to evaluate the efficacy and safety of Camostat mesylate in patients with Protein-losing enteropathy after Fontan operation.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
19
1. 4\~12 years old: Camostate mesylate 100 mg, 2 times a day 2. greater than 13 years old: Camostate mesylate 100 mg, 3 times a day
Seoul National University Hospital
Seoul, Daehak-ro Jongno-gu, South Korea
Serum albumin
change compared with baseline
Time frame: 6 months
Serum albumin
change ratio compared with baseline
Time frame: 6 months
Stool alpha-1 antitrypsin
change compared with baseline
Time frame: 6 months
Stool alpha-1 antitrypsin
change ratio compared with baseline
Time frame: 6 months
diarrhea
change of presence and number
Time frame: 6 months
ascites
ascites amount change by abdominal ultrasound
Time frame: 6 months
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