Minicore Myopathy with External Ophthalmoplegia: Clinical Trials

5 trials for Minicore Myopathy with External Ophthalmoplegia, newest first

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2 completed, 2 recruiting, 1 not yet recruiting. 1 Not applicable.

By phase and status

PhaseTrialsStatus
Not applicable1Completed 1

Follow Minicore Myopathy with External Ophthalmoplegia: new trials by email Literature Review of Minicore Myopathy with External Ophthalmoplegia trials Research Report on Minicore Myopathy with External Ophthalmoplegia

Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
The Prevalence of RYR1-related Disease
Neuromuscular Disease, Malignant Hyperthermia
Not yet recruitingKing's College London20002025-02-012025-01-24
The Natural History and Muscle Fatigability of Patients With Congenital Myopathies.
Natural history and non therapeutical therapy - Central Core Disease, Multi-Minicore Disease
RecruitingRadboud University Medical Center1002024-03-282024-08-19
The Natural History of Patients With Mutations in SEPN1 (SELENON) or LAMA2
No intervention - MDC1A, SELENON-related Myopathy
CompletedRadboud University Medical Center382020-08-262023-11-18
Probiotics in Elderly Patients With Medical Conditions
microbial cell preparation [MCP], placebo - Aging, Constipation
Not applicableCompletedUniversiti Kebangsaan Malaysia Medical Centre1002018-09-012019-07-29
Molecular and Genetic Studies of Congenital Myopathies
Central Core Disease, Centronuclear Myopathy
RecruitingBoston Children's Hospital40002003-08-012026-03-25

Narrower conditions

Myotonia Congenita (4)  ·  Myopathies, Nemaline (3)  ·  Myopathies, Structural, Congenital (3)  ·  Myopathy, Central Core (3)  ·  Muscular Diseases (2)  ·  Constipation (1)  ·  Malignant Hyperthermia (1)  ·  Muscular dystrophy congenital, merosin negative (1)  ·  Neuromuscular Diseases (1)  ·  Rigid spine syndrome (1)

Broader conditions

Congenital, Hereditary, and Neonatal Diseases and Abnormalities (4)  ·  Genetic Diseases, Inborn (4)  ·  Heredodegenerative Disorders, Nervous System (4)  ·  Musculoskeletal Diseases (4)  ·  Myotonic Disorders (4)  ·  Nervous System Diseases (4)  ·  Neurodegenerative Diseases (4)  ·  Neuromuscular Diseases (3)  ·  Muscular Diseases (2)  ·  Pathological Conditions, Signs and Symptoms (2)  ·  Signs and Symptoms (2)  ·  Body Temperature Changes (1)  ·  Hyperthermia (1)  ·  Intraoperative Complications (1)  ·  Pathologic Processes (1)

Sponsors

Radboud University Medical Center (2)  ·  Boston Children's Hospital (1)  ·  King's College London (1)  ·  Universiti Kebangsaan Malaysia Medical Centre (1)

Countries

Netherlands (2)  ·  Malaysia (1)  ·  United Kingdom (1)  ·  United States (1)

Top investigators

Alan H. Beggs, Ph.D. (1)  ·  Nicol Voermans (1)  ·  Nicol Voermans, MD PhD (1)

Results publications

PMID 10051637, PMID 10192379, PMID 10508519, PMID 11558787, PMID 12196661, PMID 12601110, PMID 12677001, PMID 15056467, PMID 15236405, PMID 16042307, PMID 17160903, PMID 17537630, PMID 19232495, PMID 19346529, PMID 19562689, PMID 19944167, PMID 19953533, PMID 21357678, PMID 33244562, PMID 34384384, PMID 37476021, PMID 38008001, PMID 42551994