Impact of Achilles Tendon Rupture on the Achilles Tendon and Calf Muscles
NCT ID: NCT05683080
Last Updated: 2025-09-04
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
60 participants
OBSERVATIONAL
2023-05-24
2025-08-01
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.
Whether Patients With Achilles Tendon Tears Have Different Lipid Levels Than Healthy People: a Retrospective Study
NCT04962243
French Achilles Tendon Surgery Cohort Study
NCT07338110
Nonoperative Treatment of Acute Achilles Tendor Rupture
NCT03704532
Achilles Tendon Lengthening With Traditional vs. Accelerated Rehab
NCT04050748
Operative Versus Non-operative Treatment of Achilles Tendon Rupture
NCT00284648
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.
Achilles Tendon Rupture
Individuals who have experienced an Achilles tendon rupture and presented to the Achilles tendon rupture clinic.
Routine Clinical Care
Participants completing the research study will receive routine clinical care
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Routine Clinical Care
Participants completing the research study will receive routine clinical care
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 16 years of age or above
Exclusion Criteria
* Inability to provide informed consent as unable to understand sufficient English
16 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospitals, Leicester
OTHER
University of Leicester
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University Hosptial of Leicester NHS Trust
Leicester, Leicester, 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.
0881
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.