Survey of Current Management of Orthopaedic Complications in CMT Patients
NCT ID: NCT02001038
Last Updated: 2015-01-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
16 participants
OBSERVATIONAL
2013-02-28
2014-11-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The target population includes orthopaedic surgeons who perform surgical procedures for foot deformities in CMT patients attending centres participating in the Inherited Neuropathies Consortium (INC).
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The orthopaedic surgeons will be asked which surgical procedures they would apply to each scenario:
* forefoot cavus,
* clawtoes and
* hindfoot varus
No medications or therapeutic agents are a component of this project.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Orthopaedic surgeons
Orthopaedic surgeons who perform surgical procedures for foot deformities in CMT patients at participants centres.
Survey
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Survey
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Willing to complete survey
Exclusion Criteria
* Inability to provide informed consent
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Hospital for Neurology and Neurosurgery, London
UNKNOWN
University of Iowa
OTHER
Children's Hospital of Philadelphia
OTHER
University of Pennsylvania
OTHER
University of Rochester
OTHER
Dubowitz Neuromuscular Centre
OTHER
Sydney Children's Hospitals Network
OTHER
Carlo Besta Neurological Institute
OTHER
Johns Hopkins University
OTHER
Vanderbilt University
OTHER
University of Washington
OTHER
National Institutes of Health (NIH)
NIH
Stanford University
OTHER
Data Management and Coordinating Center (DMCC)
OTHER
Federal, State foundation and industry support: National Institute of Health (NIH), Muscular Dystrophy Association, Charcot Marie Tooth Association
UNKNOWN
University College London Hospitals
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Prof Mary Reilly
Professor of Clinical Neurology and Consultant Neurologist
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Prof Mary Reilly
Role: STUDY_CHAIR
National Hospital for Neurology and Neurosurgery
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
National Hospital for Neurology and Neurosurgery
London, , United Kingdom
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
INC 6608
Identifier Type: -
Identifier Source: org_study_id