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CLINICAL_TRIALS ClinicalTrials.gov record update

Gait Analysis Parameter and Upper Limb Evaluation in Adult Patients With Neurological or Metabolic Pathology

This page presents selected fields from the linked source record. It does not add a medical interpretation.

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT07136844
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:27:24.904101+00:00
Published At
2025-08-22T00:00:00+00:00
Record Updated At
2025-08-22
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Neuromuscular Diseases", "Obesity (Disorder)", "Myotonic Dystrophy 1", "Myasthenic Syndrome", "Charcot Marie Tooth Disease (CMT)", "Glycogen Storage Disease Type II Pompe Disease", "Facio-Scapulo-Humeral Dystrophy", "Myasthenia Gravis", "Huntington Disease", "Progressive Supranuclear Palsy (PSP)", "Hereditary Spastic Paraplegia", "Ataxia, Spinocerebellar"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-08-22"
protocolSection.identificationModule.nctId
"NCT07136844"
protocolSection.identificationModule.officialTitle
"Gait Analysis Parameter and Upper Limb Evaluation in Adult Patients With Neurological or Metabolic Pathology"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
["NA"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Neuromuscular Diseases (protocolSection.conditionsModule.conditions)
  • Obesity (Disorder) (protocolSection.conditionsModule.conditions)
  • Myotonic Dystrophy 1 (protocolSection.conditionsModule.conditions)
  • Myasthenic Syndrome (protocolSection.conditionsModule.conditions)
  • Charcot Marie Tooth Disease (CMT) (protocolSection.conditionsModule.conditions)
  • Glycogen Storage Disease Type II Pompe Disease (protocolSection.conditionsModule.conditions)
  • Facio-Scapulo-Humeral Dystrophy (protocolSection.conditionsModule.conditions)
  • Myasthenia Gravis (protocolSection.conditionsModule.conditions)
  • Huntington Disease (protocolSection.conditionsModule.conditions)
  • Progressive Supranuclear Palsy (PSP) (protocolSection.conditionsModule.conditions)
  • Hereditary Spastic Paraplegia (protocolSection.conditionsModule.conditions)
  • Ataxia, Spinocerebellar (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.