Electrical Impedance Myography and Ultrasound as Biomarkers of Duchenne Muscular Dystrophy
NCT ID: NCT01491555
Last Updated: 2016-03-24
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
73 participants
OBSERVATIONAL
2012-04-30
2015-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Children participating in the study will come in for 10 visits over two years. Visits will take place every month at first, then less often for the remaining visits. The tests for the study itself take approximately 2hours. If participants are interested or would like to learn more about the study, please call Lavanya Madabusi at 617-919-3554 or [email protected]. All inquiries will be kept strictly confidential.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
This is a Study to Get More Information About Non Ambulatory Boys & Men With Duchenne Muscular Dystrophy
NCT01098708
Pompe Disease QMUS and EIM
NCT02742298
Innovative Ultrasound Technology in Neuromuscular Disease
NCT02104921
Studying Skeletal Muscle, Heart, and Diaphragm Imaging in Boys With Duchenne Muscular Dystrophy
NCT01451281
Longitudinal Study of the Natural History of Duchenne Muscular Dystrophy (DMD)
NCT00468832
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
DMD patients
35 boys ages 2 through 30 with DMD
No interventions assigned to this group
Control Group
35 healthy boys ages 2 through 30
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Male, age 2 - 30
1\. Male, age 2 - 30
Exclusion Criteria
2. Presence of a superimposed neuromuscular or other medical condition that substantially impacts the individual's health
1. Presence or past history of a neuromuscular disorder or other disease that substantially impacts health
2. Presence of implanted pacemaker or other electrical device.
2 Years
30 Years
MALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Beth Israel Deaconess Medical Center
OTHER
Boston Children's Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Basil Darras
Basil Darras, M.D.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Basil Darras, MD
Role: PRINCIPAL_INVESTIGATOR
Boston Children's Hospital
Seward Rutkove, MD
Role: PRINCIPAL_INVESTIGATOR
Beth Israel Deaconess Medical Center
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Children's Hospital Boston
Boston, Massachusetts, United States
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.
IRB-P00001218
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.