Page 1 of Clinical Trials for Pathologic Processes, 13801 Total Matches
- 1Active, not recruitingLast Updated: April 18, 2012Condition(s): Anemia; Anemia, Hemolytic; Anemia, Hemolytic, Autoimmune; Hemolysis; Hematologic Diseases; Autoimmune Diseases; Immune System Diseases; Pathologic Processes
- 2RecruitingLast Updated: February 27, 2012Condition(s): Ischemia; Retinal Vein Occlusion; Pathologic Processes; Retinal Diseases; Eye Diseases
- 3CompletedLast Updated: August 30, 2011Condition(s): Myocardial Infarction; Cardiovascular Diseases; Pathologic Processes
- 4Not yet recruitingLast Updated: April 9, 2012Condition(s): Ischemia; Pathologic Processes
- 5RecruitingLast Updated: August 17, 2009Condition(s): Pathological Processes
- 6CompletedLast Updated: March 24, 2010Condition(s): Pathological Processes
- 7CompletedLast Updated: May 6, 2011Condition(s): Pathological Processes in the Posterior Fossa; Dura Defects
- 8RecruitingLast Updated: January 27, 2012Condition(s): Metastatic Liver Disease
- 9CompletedLast Updated: April 11, 2012Condition(s): Malignant Solid Tumour; Liver Metastases
- 10RecruitingLast Updated: May 23, 2012Condition(s): Brain Metastases; Lung Cancer; Breast Cancer; Melanoma; Malignant Glioma
- 11CompletedLast Updated: April 5, 2012Condition(s): Fibrillation, Atrial; Atrial Fibrillation
- 12RecruitingLast Updated: July 28, 2011Condition(s): Muscular Dystrophy; Congenital Muscular Dystrophy; Fukutin-related Protein Gene; Limb Girdle; FKRP Gene; Childhood Onset LGMD; Adult Onset LGMD; POMT1; POMT2; POMGnT1; LARGE; Alpha Dystroglycan; Dystroglycanopathy; Centronuclear; Multiminicore; Multicore; Minicore; Congenital Fiber Type Disproportion; Myotubular; Nemaline; Congenital Myopathy; Neuromuscular; Rigid Spine; Phenotype-Genotype Correlation; Cough Assisted Device; Neuromuscular Disease; Respiratory Exacerbation; Invasive Ventilation; Chest Physiotherapy; Congenital Myopathies; Genetic Mutations; Hypertrophic Cardiomyopathy; Wheelchair Use; Cataract; Opthalmoplegia; Ullrich Congenital Muscular Dystrophy; Intermediate Collagen VI Myopathy; Laminin Alpha 2 Related Congenital Muscular Dystrophy; MDC1A; Merosin Deficient Congenital Muscular Dystrophy; Congenital Muscular Dystrophy Undiagnosed; Congenital Muscular Dystrophy Merosin Positive; Walker Warburg Syndrome; Muscle Eye Brain Disease; Fukuyama; Integrin Alpha 7 Deficiency; Integrin Alpha 9 Deficiency; Laminopathy; Lamin AC; SEPN 1 Related Myopathies; Bethlem Myopathy; Dystroglycanopathies; LGMD2K; LGMD2I; LGMD2L; LGMD2N; Actin Aggregation Myopathy; Cap Disease; Central Core Disease; Centronuclear Myopathy; Core Rod Myopathy; Hyaline Body Myopathy; Multiminicore Myopathy; Myotubular Myopathy; Nemaline Myopathy; Tubular Aggregate Myopathy; Zebra Body Disease Myopathy; Congenital Myopathy Other; Reducing Body Myopathy; Sarcotubular Myopathy; Spheroid Body Myopathy
- 13RecruitingLast Updated: September 13, 2010Condition(s): Diabetes; Limb Ischemia
- 14RecruitingLast Updated: July 17, 2011Condition(s): Proctitis; Proctosigmoiditis
- 15Active, not recruitingLast Updated: January 3, 2011Condition(s): Pulmonary Fibrosis
- 16RecruitingLast Updated: November 28, 2011Condition(s): Heart Failure; Arrhythmias, Cardiac
- 17RecruitingLast Updated: July 17, 2011Condition(s): Proctitis; Proctosigmoiditis
- 18Active, not recruitingLast Updated: March 28, 2011Condition(s): Emphysema; Chronic Obstructive Airway Disease; Pulmonary Emphysema; Lung Diseases
- 19Recruiting
- 20Enrolling by invitationLast Updated: April 3, 2012Condition(s): Endothelial Dysfunction; Systemic Inflammation
Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.
The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?term=Pathologic+Processes
