Standard Deviation of the Distance Between the Sural Nerve and Achilles Tendon by Ultrasound
NCT ID: NCT01112605
Last Updated: 2011-07-19
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
50 participants
OBSERVATIONAL
2010-04-30
2010-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Biomechanical and Ultrasonic Assessment of the Achilles Tendon in Vivo (MEDUSAA)
NCT02567058
Use of Ultrasonography for Measuring Achilles Tendon Thickness: a Novel Measurement Method
NCT06867211
High Volume Saline Injections for Achilles Tendinopathy
NCT01583504
Achilles Tendon Lengthening With Traditional vs. Accelerated Rehab
NCT04050748
Impact of Achilles Tendon Rupture on the Achilles Tendon and Calf Muscles
NCT05683080
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.
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
otherwise healthy persons
healthy persons, no major trauma or surgery of ankle or calves, no bone or muscle disease, age 18-60
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
* age 18-60
Exclusion Criteria
* major trauma to the leg or ankle in present or past
* surgery of leg or ankle in the past
* mental disabilities
18 Years
60 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Meir Medical Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Meir Medical Center
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Omer Mei-Dan, Dr.
Role: PRINCIPAL_INVESTIGATOR
Meir Medical Center
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Meir Medical Center
Kfar Saba, , Israel
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.
MMC09155-09CTIL
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.