biliary atresia

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Information
Disease name
biliary atresia
Disease ID
DOID:13608
Description
"A cholestasis characterized by blockage of the ducts that carry bile from the liver to the gallbladder." [url:http\://en.wikipedia.org/wiki/Biliary_atresia, url:http\://www.nlm.nih.gov/medlineplus/ency/article/000215.htm]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT06219993 Active, not recruiting Robot-assisted Modified Kasai Portoenterostomy Versus Open Kasai Portoenterostomy for Biliary Atresia December 21, 2023 December 30, 2025
NCT02922751 Active, not recruiting FibroScan™ in Pediatric Cholestatic Liver Disease (FORCE) November 16, 2016 December 2024
NCT00294684 Completed N/A A Randomized, Double-Blinded, Placebo-Controlled Trial of Corticosteroid Therapy Following Portoenterostomy November 2005 January 2013
NCT05517317 Completed Phase 1 Autologous BMNC Infusion for Liver Cirrhosis in Children With BA January 1, 2015 May 30, 2022
NCT00166868 Completed N/A Use of Probiotics to Prevent Cholangitis in Children With Biliary Atresia After the Kasai Portoenterostomy December 2003 July 2012
NCT01063699 Completed N/A Survival With Own Liver of Conventional Versus Laparoscopic Kasai for Biliary Atresia August 2003 September 2007
NCT01322386 Completed Phase 1 Gastrointestinal Microbiota in Primary Sclerosing Cholangitis and Biliary Atresia With Vancomycin May 2007 January 2012
NCT01443572 Completed N/A The Comparison of Desflurane and Sevoflurane on Postoperative Recovery and Hepatic Function of Biliary Atresia Patients During Kasai Operation September 2011 July 2014
NCT01854827 Completed Phase 1/Phase 2 Safety Study of Intravenous Immunoglobulin (IVIG) Post-Portoenterostomy in Infants With Biliary Atresia October 2013 July 2016
NCT02292862 Completed Maternal Microchimerism in Lymph Nodes of Infants With Biliary Atresia at Time of Kasai's Operation November 2012 November 2014
NCT02471209 Completed Biliary Atresia, Hepatic Buffer Response and Sevoflurane January 2012 February 2014
NCT02652533 Completed Ultrasound Shear Wave Elastography Evaluation of Suspected and Known Biliary Atresia September 2016 July 2019
NCT03395028 Completed Early Phase 1 GCSF Adjunct Therapy for Biliary Atresia January 15, 2018 January 31, 2020
NCT03499249 Completed Phase 2 N-Acetylcysteine in Biliary Atresia After Kasai Portoenterostomy May 18, 2018 March 23, 2024
NCT04524390 Completed Phase 2 Evaluation of Maralixibat in Biliary Atresia Response Post-Kasai July 8, 2021 February 7, 2024
NCT04778735 Completed N/A Investigation of Mortality, Morbidity and Risk Factors After Pediatric Liver Transplantation February 24, 2021 April 4, 2022
NCT00007033 Completed N/A Study of Magnesium Sulfate in Children With Reduced Bone Density Secondary to Chronic Cholestatic Liver Disease October 2000
NCT05925543 Completed Outcome of Kasai Portoenterostomy in Biliary Atresia in Upper Egypt January 1, 2019 December 30, 2019
NCT06163417 Completed Laparoscopic Kasai Has Similar Anesthetic Outcomes to Open Kasai January 1, 2011 March 28, 2023
NCT05426733 Enrolling by invitation Phase 3 An Open-label Extension Study to Evaluate Long-term Efficacy and Safety of Odevixibat in Children With Biliary Atresia July 5, 2022 December 31, 2026
NCT06260566 Not yet recruiting Phase 1 Tolerability of Enteral NAC in Infants May 2024 February 2027
NCT03890536 Not yet recruiting Intestinal Microbiome Composition in Infants With Biliary Atresia (BA) December 2023 March 2032
NCT06121375 Not yet recruiting Phase 2/Phase 3 Study to Assess Efficacy, Safety, Tolerability, Pharmacokinetics (PK), and Pharmacodynamics (PD) of Obeticholic Acid (OCA) Compared to Placebo in Pediatric Participants With Biliary Atresia, Post-hepatoportoenterostomy March 2024 December 2027
NCT05783518 Not yet recruiting Phase 4 Effect of Desflurane on Pediatric Acute Respiratory Distress Syndrome After Living Donor Liver Transplant Recipients March 27, 2023 October 31, 2023
NCT05925309 Recruiting N/A Preventive Effect of Prophylactic Oral Antibiotics Against Cholangitis After Kasai Portoenterostomy July 1, 2023 July 31, 2027
NCT03273049 Recruiting Mapping Disease Pathways for Biliary Atresia July 21, 2016 July 21, 2027
NCT03842150 Recruiting Development and Validation of a Screening Score for the Biliary Atresia in Infantile Cholestasis: A Prospective Study June 1, 2014 December 31, 2025
NCT05072626 Recruiting High Medium-chain Triglyceride Nutritional Support in Infants With Biliary Atresia October 11, 2021 December 31, 2026
NCT05181332 Recruiting Predictive Models of Hepatic Decompensation and Survival Outcomes in Pediatric Patients With Cirrhosis January 1, 2021 December 31, 2024
NCT05399745 Recruiting BILACO Trial: Biliary Atresia - a Severe Complex Congenital Liver Disease March 1, 2020 December 31, 2040
NCT00345553 Recruiting Biliary Atresia Study in Infants and Children May 16, 2006 May 2029
NCT05464303 Recruiting Definition for Biliary Atresia Associated Cholangitis After Surgery July 15, 2022 December 31, 2022
NCT00061828 Recruiting A Prospective Database of Infants With Cholestasis April 21, 2004 May 2029
NCT05521152 Recruiting Phase 3 Norepinephrine for Prevention of Intraoperative Hypotension in Infants Undergoing Kasai Portoenterostomy May 1, 2022 April 1, 2024
NCT01793168 Recruiting Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford July 2010 December 2100
NCT02137668 Recruiting Phase 1 Treating Primary Sclerosing Cholangitis and Biliary Atresia With Vancomycin July 2010 July 2028
NCT05848310 Recruiting Preoperative Serum FGF19 in the Prognosis of Biliary Atresia October 15, 2023 August 2024
NCT05909033 Recruiting Early Predictors for the Short Term Native Liver Survival in Patients With Biliary Atresia After Kasai Procedure May 20, 2017 July 1, 2023
NCT04272515 Recruiting N/A Molecular Characterization for Understanding Biliary Atresia February 7, 2021 February 7, 2032
NCT04336722 Recruiting Phase 3 Efficacy and Safety of Odevixibat in Children With Biliary Atresia Who Have Undergone a Kasai HPE (BOLD) July 8, 2020 July 31, 2026
NCT04373941 Recruiting Phase 2 Part II: Granulocyte-Colony Stimulating Factor Adjunct Therapy for Biliary Atresia September 1, 2023 October 31, 2025
NCT06447051 Recruiting Efficacy of New Post Kasai ILBS Protocol in Biliary Atresia. June 6, 2024 March 31, 2026
NCT06184971 Recruiting Biliary Atresia Research Network Northeast May 6, 2024 December 2024
NCT01774487 Terminated Phase 2 Pentoxifylline Therapy in Biliary Atresia February 4, 2013 February 20, 2023
NCT05321524 Terminated Phase 2 Obeticholic Acid in Pediatric Subjects With Biliary Atresia July 1, 2015 March 9, 2023
NCT03898765 Unknown status N/A Dry Blood Spot Screening Test for Biliary Atresia(DBS-SCReBA) April 1, 2019 December 31, 2021
NCT04506021 Unknown status A Real World Study on Clinical Efficacy of Bicarbonate Ringer's Solution in Biliary Atresia Children August 2020 October 2021
NCT04260503 Unknown status Gut Microbiome in Biliary Atresia May 21, 2019 May 20, 2022
NCT02503384 Unknown status Clinical and Basic Study for Pediatric Liver Transplantation July 2015 September 2018
NCT04961034 Unknown status N/A Peri Kasai Portoenterostomy Anchoring of the Jejunal Loop January 2015 December 20, 2023
NCT03667534 Unknown status Dry Blood Spot Screening Test for Neonatal Cholestasis Patients September 9, 2018 September 9, 2021
NCT00155194 Unknown status Evaluation of Immune Function in Biliary Atresia Children With Prolonged Jaundice April 2004
NCT00539565 Unknown status Phase 3 RCT of Steroids Following Kasai Portoenterostomy for Biliary Atresia. January 2000 September 2008
NCT01745991 Unknown status Trail to Investigate the Effectiveness of CoSeal in Reducing Adhesions Following the Kasai Hepatoportoenterostomy for Biliary Atresia December 2012 December 2017
Disase is a (Disease Ontology)
DOID:13580
Cross Reference ID (Disease Ontology)
GARD:12010
Cross Reference ID (Disease Ontology)
ICD10CM:Q44.2
Cross Reference ID (Disease Ontology)
ICD9CM:751.61
Cross Reference ID (Disease Ontology)
MESH:D001656
Cross Reference ID (Disease Ontology)
MIM:210500
Cross Reference ID (Disease Ontology)
NCI:C34421
Cross Reference ID (Disease Ontology)
ORDO:30391
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:77480004
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0005411
Exact Synonym (Disease Ontology)
Atresia of bile duct
Exact Synonym (Disease Ontology)
biliary atresia, congenital
Exact Synonym (Disease Ontology)
Congenital biliary atresia
HPO Human Phenotype ID (Human Phenotype Ontology)
HP:0005912
MeSH unique ID (MeSH (Medical Subject Headings))
D001656