Clinical Trials

Showing trials with last updates posted in 2021.

NCT01403402 | RECRUITING
4000 participants

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

Study Type:
OBSERVATIONAL
Last Updated:
2021-08-09
Start Date:
2009-09-30
Completion:
2029-09-30
Conditions
  • Congenital Muscular Dystrophy With ITGA7 (Integrin Alpha-7) Deficiency
  • Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy)
  • Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations)
  • Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan)
  • Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan and Epilepsy)
  • Alpha-Dystroglycanopathy (Dystroglycanopathy, Congenital With or Without Mental Retardation (Formerly MDC1C))
  • Alpha-Dystroglycanopathy (Fukuyama CMD)
  • Alpha-Dystroglycanopathy (LGMDR09 FKRP Related (Formerly LGMD2I))
  • Alpha-Dystroglycanopathy (LGMDR11 POMT1 Related (Formerly LGMD2K))
  • Alpha-Dystroglycanopathy (LGMDR13 FKTN Related (Formerly LGMD2M))
  • Alpha-Dystroglycanopathy (LGMDR14 POMT2 Related (Formerly LGMD2N))
  • Alpha-Dystroglycanopathy (LGMDR15 POMGnT1 Related (Formerly LGMD2O))
  • Alpha-Dystroglycanopathy (LGMDR19 GMPPB Related (Formerly LGMD2T))
  • Alpha-Dystroglycanopathy (LGMDR20 ISPD Related (Formerly LGMD2U))
  • Alpha-Dystroglycanopathy (LGMDR24 POMGnT2 Related)
  • Alpha-Dystroglycanopathy (Muscle Eye Brain Disease (MEB))
  • Alpha-Dystroglycanopathy (Walker Warburg Syndrome (WWS))
  • Choline Kinase B Receptor - CHKB
  • Collagen VI Related Disorders
  • Collagen XII Related Disorders
  • Congenital Muscular Dystrophy Not Otherwise Specified (Including Merosin Positive)
  • Congenital Muscular Dystrophy With Cataracts and Intellectual Disability (MDCCAID)
  • Congenital Muscular Dystrophy With Joint Hyperlaxity
  • Congenital Muscular Dystrophy With Rigid Spine Related to ACTA1
  • Emery-Dreifuss Muscular Dystrophy
  • GOLGA2-related Congenital Muscle Dystrophy With Brain Involvement
  • LMNA Related Disorders
  • Merosin Deficient CMD (Full or Partial)
  • Nesprin Related MD (SYNE1)
  • SELENON Related Disorders (Previously Known as SEPN1)
  • SELENON Related Myopathy (Aka SEPN1)
  • Telethonin CMD
  • Congenital Myasthenic Syndrome
  • Limb-Girdle Muscular Dystrophy
  • LGMDD01 - DNAJB6 (Formerly LGMD1D)
  • LGMDD05 - Collagen VI Related Bethlem Myopathy (Dominant)
  • LGMDR07 - Telethonin (TCAP) Related (Formerly LGMD2G)
  • LGMDR08 - TRIM Related (Formerly LGMD2H)
  • LGMDR09 - FKRP Related (Formerly LGMD2I)
  • LGMDR10 - Titin (TTN) Related (Formerly LGMD2J)
  • LGMDR11 - POMT1 Related (Formerly LGMD2K)
  • LGMDR13 - Fukutin (FKTN) Related (Formerly LGMD2M)
  • LGMDR14 - POMT2 Related (Formerly LGMD2N)
  • LGMDR15 - POMGnT1 Related (Formerly LGMD2O)
  • LGMDR16 - DAG1 Related Dystroglycanopathy (Formerly LGMD2P)
  • LGMDR17 - Plectin (PLEC) Related (Formerly LGMD2Q)
  • LGMDR18 - TRAPPC11 Related (Formerly LGMD2S)
  • LGMDR19 - GMPPB Related (Formerly LGMD2T)
  • LGMDR20 - ISPD Related (Formerly LGMD2U)
  • LGMDR22 - Collagen VI Related Bethlem Myopathy (Recessive)
  • LGMDR23 - LAMA2 Related
  • LGMDR24 - POMGnT2 Related
No Results Yet
NCT04993989 | COMPLETED
843 participants

A Pharmacy-based Study to Learn More About How Well Iberogast Works, How it Affects the Body, How it is Used, and User Satisfaction in Patients With Functional and Motility-related (Stomach and Bowel Movement-related) Gastrointestinal Diseases, Including Irritable Bowel Syndrome

Study Type:
OBSERVATIONAL
Last Updated:
2021-08-06
Start Date:
2017-11-16
Completion:
2018-04-18
Conditions
  • Functional and Motility Related Gastrointestinal Disorders Such as Irritable Bowel Syndrome and Functional Dyspepsia
Interventions
  • DRUG
No Results Yet
Previous
Sorted by latest updates
Next
Showing 40 trials per page