International Registry for TRPM3-associated Disorders
NCT07690111 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 100
Last updated 2026-07-08
Summary
The goal of the TRPM3Care-registry is to record the disease progression of patients with TRPM3-associated disorders. This allows us to compare the disease progression and the success of different therapies, as well as to examine their impact on quality of life.
Conditions
- TRPM3
Sponsors & Collaborators
-
Charite University, Berlin, Germany
lead OTHER
Principal Investigators
-
Lena-Luise Becker, Dr. med. · Charité- Universitätsmeidzin Berlin- Neuropediatrics
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-01-01
- Primary Completion
- 2036-01-01
- Completion
- 2036-12-31
Countries
- Germany
Study Locations
More Related Trials
-
Analysis of Oculo-motor Deficiencies Associated With FMR1 Gene Expression (Genetic Abnormality Predisposing to a Neurodegenerative Disease)
NCT00763191 ·Status: TERMINATED ·Phase: NA
-
Natural History of Oculo-Pharyngeal Muscular Dystrophy (OPMD) - Israel National OPMD Registry
NCT07146256 ·Status: RECRUITING
-
Natural History With Focus on Oncological Risk Evaluation in Pediatric Patients With PTEN Pathogenic Variants
NCT06805734 ·Status: RECRUITING
-
The Natural History of TRPV4 Neuropathy
NCT05600764 ·Status: RECRUITING
-
Pompe & Pain - Study to Assess Nociceptive Pain in Adult Patients With Pompe Disease
NCT05272969 ·Status: RECRUITING
-
Krabbe Disease Global Patient Registry
NCT02993796 ·Status: RECRUITING
-
Monitoring of Early Disease Progression in Hereditary Transthyretin Amyloidosis
NCT03431896 ·Status: COMPLETED
-
Pompe Disease Registry Protocol
NCT00231400 ·Status: RECRUITING
-
Autosomal Dominant Retinitis Pigmentosa: Prevalence of Known Genes Identification of New Loci / Genes
NCT01235624 ·Status: COMPLETED ·Phase: NA
-
GM1 and GM2 Gangliosidosis PROspective Neurological Disease TrajectOry Study (PRONTO)
NCT05109793 ·Status: COMPLETED
-
International Primary Ciliary Dyskinesia (PCD) Registry
NCT02419365 ·Status: RECRUITING
-
A Natural History Study of Angelman Syndrome
NCT07417137 ·Status: RECRUITING
-
MPN Childhood Registry
NCT07410247 ·Status: RECRUITING
-
Registry for Primary Ciliary Dyskinesia
NCT03271840 ·Status: COMPLETED
-
Sun May Arise on SMA : Newborn Screening of Spinal Muscular Atrophy in Belgium
NCT03554343 ·Status: COMPLETED
-
Natural History of SMA
NCT05755451 ·Status: RECRUITING
-
Clinical Presentation and Renal Outcome of Patients With Tuberous Sclerosis Complex and/or Renal Angiomyolipoma in the Great West Region of France
NCT02887781 ·Status: RECRUITING
-
TRAMmoniTTR Study Genetic Screening of an At-risk Population for hATTR and Monitoring of TTR Positive Subjects
NCT03237494 ·Status: COMPLETED
-
A Natural History Study to TRACK Brain and Spinal Cord Changes in Individuals with Friedreich Ataxia (TRACK-FA)
NCT04349514 ·Status: ACTIVE_NOT_RECRUITING
-
Understanding the Natural History Early in the Course or Presentation of Friedreich Ataxia
NCT06560346 ·Status: WITHDRAWN
-
Friedreich Ataxia Global Clinical Consortium UNIFIED Natural History Study
NCT06016946 ·Status: RECRUITING
-
Registry Gangliosidoses
NCT04624789 ·Status: UNKNOWN
-
A National Retrospective Population Based Cohort Study of the Natural History of Ataxia Telangiectasia
NCT04991701 ·Status: UNKNOWN
-
COL4A1 Gene Related Cerebra-retinal Angiopathy
NCT01097564 ·Status: COMPLETED
-
International Primary Ciliary Dyskinesia Cohort
NCT03517865 ·Status: ACTIVE_NOT_RECRUITING