Biliary Atresia, Kasai Portoenterostomy Status Clinical Trial
| Verified date | November 2014 |
| Source | Yonsei University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Korea: Food and Drug Administration |
| Study type | Interventional |
In this clinical study, meloxicam will be used to the patients who are older than 2 years and underwent Kasai portoenterostomy to treat their biliary atresia before. Before and after the medication, their liver stiffness scores will be checked using hepatic Fibroscan. Liver stiffness scores will be compared before and after the medication of meloxicam, and the roll of the COX-2 inhibitor (meloxicam) in the patients with biliary atresia in releasing their hepatic fibrosis. Also, the side effect of the drug will be checked. The intervention drug, meloxicam is safe medicine which is used to treat pain or inflammation caused by osteoarthritis or rheumatoid arthritis in adults and children who are at least 2 years old. It may also be used for purposes not listed in the medication guide. It will be taken once a daily with a dose of 0.125 mg/kg/day (high-dose group) or 0.06 mg/kg/day (low-dose group). After 6 months of medication, the maintenance will be decided by the comparison of liver stiffness score before and after the intervention.
| Status | Completed |
| Enrollment | 50 |
| Est. completion date | December 2011 |
| Est. primary completion date | June 2011 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | 2 Years to 17 Years |
| Eligibility |
Inclusion Criteria: 1. Patients who had undergone a Kasai portoenterostomy for BA, and who were postoperatively managed in our outpatient clinic 2. Patients who made informed consent for clinical study of COX-2 inhibitor 3. Patients who were followed up with liver fibroscan study 4. Patients who were over 2 years old and less than or equal to 17 years Exclusion Criteria: 1. Patients who were impossible to join the clinical study because of their underlying diseases (renal disease, liver disease, diabetes mellitus, GI disease, including bleeding, perforation, or ulceration, etc.) other than biliary atresia, ii) H. pylori infection, iii) asthma, iv) nasal polyp, v) hypertension, vi) hematologic disease, vii) coagulopathy, viii) cardiac disease, ix) vascular disease 2. Patients who did not get the drug (COX-2 inhibitor) 3. Patients who did not check liver fibroscan 4. Patients who were impossible to join the clinical study because of their complication after Kasai portoenterostomy 5. Patients who did not make informed consent for clinical study of COX-2 inhibitor 6. Patients who cannot take drug because of their allergy, skin disease or asthma attack to drug (COX-2 inhibitor) 7. Patients who were decided to withdraw because of their severe drug adverse events |
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Yonsei University |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | liver stiffness score on FibroScan | statistical comparison between liver stiffness score of study group (COX-2 inhibitor group) and control group (no intervention group) before and after the clinical study using t-test, chi-square and logistic regression test) | from 6 to 12 years | No |