Changes of Plantar Pressure After Knee Reconstructive Surgery
NCT ID: NCT02906735
Last Updated: 2016-10-19
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.
UNKNOWN
50 participants
OBSERVATIONAL
2016-09-30
2017-11-30
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.
Pedobarographic Changes After Forefoot Reconstruction
NCT02643485
Biomechanical Functional Evaluation of Plantar Pressures After Foot and Ankle Surgeries
NCT06090357
Effects of Different Foot Structures on Plantar Fasciitis and Therapeutic Footwear Intervention
NCT01363375
3D Multisegment Foot Model Used for the Clinical Outcome After Ankle and Hindfoot Reconstruction
NCT04822558
Plantar Forces Mid-term After Hemiarthroplasty With HemiCap for Hallux Rigidus
NCT02904447
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.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Study group
Patients with knee surgery undergo plantar foot pressure measurement pre- and postoperatively
Surgery
Implantation of knee joint prosthesis or deviation osteotomies of the knee
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Surgery
Implantation of knee joint prosthesis or deviation osteotomies of the knee
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Technical University of Munich
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Harrasser
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Norbert Harrasser
Role: PRINCIPAL_INVESTIGATOR
Klinikum rechts der Isar
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Klinikum rechts der Isar
Munich, Bavaria, Germany
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
TUM1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.