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Immunophenotyping and Xist Gene in AML
Condition(s):Acute Myeloid LeukemiaLast Updated:July 9, 2020Not yet recruiting
Gene Abnormality: 999 Clinical Trials, Page 4 of 100
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Ibrutinib Combined With Rituximab for Treatment of Relapsed Refractory MYD88 and CD79A/B (or CD79B Alone) DLBCL Who Have Received at Least Two Prior Therapies
Condition(s):DLBCL; MYD88 Gene Mutation; CD79A Gene Mutation; CD79B Gene Mutation; Relapse; Refractory LymphomaLast Updated:August 6, 2021Not yet recruiting
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Neonatal Seizure Registry, GEnetics of Post-Neonatal Epilepsy
Condition(s):Neonatal Seizure; Hypoxic-Ischemic Encephalopathy; Stroke; Intracranial Hemorrhage; Epilepsy; Gene AbnormalityLast Updated:May 4, 2022Recruiting
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Stool Testing for Pancreatic Cancer
Condition(s):Pancreatic CancerLast Updated:January 19, 2021Completed
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Analysis of Oculo-motor Deficiencies Associated With FMR1 Gene Expression (Genetic Abnormality Predisposing to a Neurodegenerative Disease)
Condition(s):Pre-mutation on FMR1 GeneLast Updated:December 10, 2012Terminated
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Genetics of Central Nervous System Arteriovenous Malformations (GENE-MAV)
Condition(s):Arteriovenous MalformationsLast Updated:March 7, 2022Recruiting
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Identification of Genetic Mutations Involved in Chiari Type I Malformations
Condition(s):Chiari Malformation, Type 1Last Updated:December 21, 2021Not yet recruiting
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Prospective Multicenter Study on the Identification of Genetic Abnormalities Predisposing to Vasospasm From a Privileged Model: the Primary Raynaud’s Phenomenon
Condition(s):Primary Raynaud’s Phenomenon (PR); Genetic Mutations Causing PR; Study of Patients and Their Relatives (With or Without Primary PR)Last Updated:June 24, 2020Completed
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Genetic Study of the FBN1 Gene and Fibrillin-1 Abnormalities in Choctaw Native Americans and Other Patients With Systemic Sclerosis
Condition(s):Systemic SclerosisLast Updated:June 24, 2005Unknown status
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Genes Causing Ebstein’s Anomaly
Condition(s):Heart Septal Defects, Ventricle; Heart Defects, Congenital; Double Outlet Right Ventricle; Truncus Arteriosus, PersistentLast Updated:July 2, 2017Completed