Page 1 of Clinical Trials for "Urea Cycle Disorders, Inborn", 45 Total Matches
- 1Not yet recruitingLast Updated: February 29, 2012Condition(s): Urea Cycle Disorders
- 2Enrolling by invitationLast Updated: June 22, 2011Condition(s): Urea Cycle Disorders
- 3RecruitingLast Updated: February 13, 2012Condition(s): Urea Cycle Disorders
- 4RecruitingLast Updated: January 25, 2012Condition(s): Urea Cycle Disorders; Carbamoylphosphate Synthetase I Deficiency Disease; Ornithine Transcarbamylase Deficiency Disease; Citrullinemia
- 5CompletedLast Updated: July 14, 2009Condition(s): Urea Cycle Disorders
- 6CompletedLast Updated: August 19, 2010Condition(s): Urea Cycle Disorders
- 7Active, not recruitingLast Updated: March 19, 2012Condition(s): Urea Cycle Disorders
- 8CompletedLast Updated: August 19, 2010Condition(s): Urea Cycle Disorders
- 9CompletedLast Updated: August 19, 2010Condition(s): Urea Cycle Disorders
- 10RecruitingLast Updated: February 8, 2012Condition(s): Brain Diseases, Metabolic, Inborn; Amino Acid Metabolism, Inborn Errors; Urea Cycle Disorders
- 11RecruitingLast Updated: March 6, 2012Condition(s): Urea Cycle Disorders
- 12CompletedLast Updated: February 8, 2012Condition(s): Brain Diseases, Metabolic, Inborn; Urea Cycle Disorder; Ornithine Transcarbamylase Deficiency
- 13RecruitingLast Updated: December 6, 2011Condition(s): Urea Cycle Disorders, Inborn; Inborn Errors of Metabolism; Propionic Acidemia; Methylmalonic Acidemia; Carbamyl Phosphate Synthetase Deficiency
- 14Active, not recruitingLast Updated: February 15, 2012Condition(s): Argininosuccinic Aciduria; Amino Acid Metabolism, Inborn Errors; Urea Cycle Disorders
- 15CompletedLast Updated: January 14, 2010Condition(s): Urea Cycle Disorders
- 16RecruitingLast Updated: June 23, 2005Condition(s): Amino Acid Metabolism, Inborn Errors
- 17RecruitingLast Updated: March 20, 2012Condition(s): Argininosuccinic Aciduria; Carbamoyl-Phosphate Synthase I Deficiency; Citrullinemia; Ornithine Carbamoyltransferase Deficiency; Hyperargininemia; N-Acetylglutamate Synthase Deficiency
- 18CompletedLast Updated: September 28, 2009Condition(s): Hepatic Encephalopathy; Urea Cycle Disorders
- 19CompletedLast Updated: June 23, 2005Condition(s): Amino Acid Metabolism, Inborn Errors
- 20TerminatedPhase I Pilot Study of Liver-Directed Gene Therapy for Partial Ornithine Transcarbamylase DeficiencyLast Updated: June 23, 2005Condition(s): Ornithine Transcarbamylase Deficiency Disease
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/?cond=%22Urea+Cycle+Disorders%2C+Inborn%22
