Search for Clinical Trial Results
Glycogen Storage Disease Type I - 40 Studies Found
| Status | Study |
| Active, not recruiting |
Study Name: Comparison of the Effect of a Novel Starch (Glycosade) Versus Gastrostomy Tube-Dextrose Infusion on Overnight Euglycaemia Control in Children With Glycogen Storage Disease Type I: Open Label Demonstration Trial Condition:
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| Completed |
Study Name: Overnight Feeding Study in Glycogen Storage Disease Type 1 Condition: Glycogen Storage Disease Type 1 (GSD 1) Date: 2013-10-08 Interventions: Other: overnight nutrition regime Patients receive the specified overnight nutrition regimen |
| Recruiting |
Study Name: Biomarker for Glycogen Storage Diseases Condition:
Date: 2013-05-10 Interventions: Other: Glycogen Storage Disease type Ia patients The participants will have one blood draw for this stud |
| Withdrawn |
Study Name: High Protein and Exercise Therapy Plus Nocturnal Enteral Feeding in Juvenile-onset Pompe Disease Condition: Glycogen Storage Disease Type II Date: 2012-08-01 Interventions: Other: High Protein and Exercise Therapy along-with Nocturnal Enteral Feeding |
| Completed |
Study Name: A Prospective, Observational Study in Patients With Late-Onset Pompe Disease Condition: Glycogen Storage Disease Type II Date: 2004-02-10 |
| Completed |
Study Name: A Study of the Safety and Efficacy of rhGAA in Patients With Infantile-onset Pompe Disease Condition: Glycogen Storage Disease Type II Date: 2003-04-22 Interventions: Biological: Myozyme 20 mg/kg qow or 40mg/kg qow Othe |
| Completed |
Study Name: Extension Study of Patients With Infantile-Onset Pompe Disease Who Were Previously Enrolled in Protocol AGLU01602 Condition: Glycogen Storage Disease Type II Date: 2005-08-01 Interventions: Biological: Myozyme 20 mg/kg qow or 40 mg/kg qow Oth |
| Recruiting |
Study Name: Respiratory Muscle Training in L-Onset Pompe Disease (LOPD) Condition: Glycogen Storage Disease Type II Date: 2016-06-13 Interventions:
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