polyneuropathy

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Information
Disease name
polyneuropathy
Disease ID
DOID:1389
Description
"A peripheral system disease that is characterized by damage affecting peripheral nerves (peripheral neuropathy) in roughly the same areas on both sides of the body, featuring weakness, numbness, pins-and-needles, and burning pain." [url:https\://en.wikipedia.org/wiki/Polyneuropathy, url:https\://www.virginiamason.org/polyneuropathy]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT00259974 Completed Phase 3 RIMAG Study: Trial of Rituximab Versus Placebo in Polyneuropathy Associated With Anti-MAG IgM Monoclonal Gammopathy April 2006 January 2010
NCT00614562 Completed Phase 1 Neurally Adjusted Ventilatory Assist (NAVA) in Patients With Critical Illness Associated Polyneuropathy / or Polymyopathy (CIP/M) January 2008 December 2010
NCT01076478 Completed Phase 4 Asian Study on Cilostazol Effectivity in Neuropathies of Diabetes Mellitus Type 2-A Pilot Study in the Philippines March 2004 November 2009
NCT01302275 Completed Phase 4 Oxcarbazepine for the Treatment of Chronic Peripheral Neuropathic Pain February 2011 May 2013
NCT01450163 Completed Phase 3 Evaluate The Efficacy and Safety Of Pregabalin In Prevention, Reduction of Oxaliplatin-Induced Painful Neuropathy August 2011 December 2014
NCT02442986 Completed Neurological Outcome in Surgical and Non-surgical Septic Patients November 2012 March 2017
NCT02706314 Completed Impact of Human Blood Serum From Critically Ill Patients on Human Colon Neuronal Networks. March 2016 April 16, 2019
NCT02846844 Completed Patients With Chemotherapy-induced Polyneuropathy Are Treated With an Integrated Program Including Massage, Mobilization in Posture and Transport Layers, Physical Exercises or With Whole-body Vibration Platform Training June 2010 October 2015
NCT03373370 Completed Early Diagnosis of TTR Amyloidosis by Use of Molecular Biology March 17, 2017 December 10, 2021
NCT04201418 Completed A Multicenter Observational Study to Evaluate the Effectiveness of Patisiran in Patients With Polyneuropathy of ATTRv Amyloidosis With a V122I or T60A Mutation December 18, 2019 May 24, 2022
NCT05560555 Completed Retrospective Study Collecting Neurological Follow-up of Hereditary Transthyretin Amyloidosis (ATTRv) Patients Included in B3461028 and B3461045. October 24, 2022 November 15, 2022
NCT05040373 Recruiting Patisiran-Lipid Nanoparticle (LNP) Pregnancy Surveillance Program August 1, 2020 October 12, 2030
NCT05950867 Recruiting N/A Prevalence of Wild-type TTR Cardiac Amyloidosis in Patients With Polyneuropathy of Unknown Cause. July 28, 2023 June 1, 2026
NCT06414746 Recruiting Hereditary Transthyretin Amyloidosis Polyneuropathy in Patients With Carpal Tunnel Syndrome in Russia December 29, 2023 December 31, 2024
NCT01088256 Terminated Phase 2 Efficacy of Etoricoxib on Peripheral Hyperalgesia February 2011 August 2012
NCT00832572 Terminated Phase 4 Study of Ranexa in Patients With Coronary Artery Disease and Painful Polyneuropathy January 2009 June 2009
NCT02666456 Unknown status The Influence of Sensory Phenotype on the Risk of Developing Neuropathic Pain April 2016
NCT01047488 Unknown status Phase 4 Imipramine and Pregabalin Combination in Painful Polyneuropathy February 2010 March 2013
NCT02033057 Unknown status Phase 4 Muscular Electrostimulation of the Sedated and Mechanically Ventilated Critically Ill Patient. Analysis of the Effect on Acquired Muscular Weakness and Its Clinical Consequences. October 2012 October 2014
NCT02566941 Withdrawn N/A Neuromuscular Electrical Stimulation in the Critically Ill October 1, 2015 May 30, 2018
NCT00723918 Withdrawn Phase 2 Combination of an Investigational Cannabinoid and Methadone for HIV-associated Neuropathy April 2009 January 2010
Disase is a (Disease Ontology)
DOID:574
Cross Reference ID (Disease Ontology)
ICD10CM:A69.22
Cross Reference ID (Disease Ontology)
MESH:D011115
Cross Reference ID (Disease Ontology)
NCI:C26951
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:193166009
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0152025
HPO alt_id (Human Phenotype Ontology)
HP:0006941
HPO alt_id (Human Phenotype Ontology)
HP:0007287
HPO Human Phenotype ID (Human Phenotype Ontology)
HP:0001271
MedGen concept unique identifier (MedGen Concept name)
C0152025
MedGen unique identifier (MedGen Concept name)
57502