Anthropometric Predictability of Full-Thickness Peroneus Longus and Semitendinosus Autograft Size
July 27, 2026 updated by: Fevzi Gurkan Aslan, Karadeniz Technical University
Anthropometric Predictability of Full-Thickness Peroneus Longus and Semitendinosus Autograft Size: A Comparative Analysis
The study is aimed to determine correlation between autografts used in anterior cruciate ligaments and anthropometric variables e.g.
height, sex, weight, BMI etc..
Study Overview
Status
Completed
Conditions
Detailed Description
Categorical data: Age, Sex, Height, Weight, BMI, Preoperative parameters: cruris length, cruris circumference, thigh length, thigh circumference Intraoperative Info: Tendon Type, Tendon length (total-muscular part-tendinoz part), Graft Length, Graft Diameter.
After the data collected, correlation analysis will be held and determine the both tendons preoperative size predictability before acl reconstruction surgery.
Study Type
Observational
Enrollment (Actual)
180
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Trabzon, Turkey (Türkiye)
- Karadeniz Technical University, Orthopedic and Traumatology Department
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients who will apply to our center due to ACL ligament injury and will be decided to undergo surgical treatment will be included in the study if they volunteer to participate.
Description
Inclusion Criteria:
- Ages between 18-45 years
- Diagnosed Acl rupture preoperavitely with mri imaging
- Diagnosed Acl rupture and having symptoms related to acl rupture
- Eligible for harvesting same side semitendinosus or peroneous longus tendon
Exclusion Criteria:
- Previous surgery history on donor side knee or ankle
- Congenital defect on donor extremity
- Multiple Ligament Injury History
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Semitendinosus Tendon
The participiants underwent acl reconstruction with semitendinosus tendon autograft
|
Anterior cruciate ligament reconstruction surgery with semitendinosus tendon autograft
Anterior cruciate ligament reconstruction surgery with peroneus longus autograft
|
|
Peroneus Longus Tendon
The participiants underwent acl reconstruction with peroneus longus tendon autograft
|
Anterior cruciate ligament reconstruction surgery with semitendinosus tendon autograft
Anterior cruciate ligament reconstruction surgery with peroneus longus autograft
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation Between Preoperative Anthropometric Variables and Autograft Dimensions
Time Frame: Intraoperatively
|
To assess the correlation between preoperative anthropometric measurements and intraoperative autograft dimensions
|
Intraoperatively
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparison of Predictability Between Peroneus Longus and Semitendinosus Tendons
Time Frame: Preoperatively at surgery day
|
To determine whether the predictability of tendon dimensions based on anthropometric variables,height(cm), weight(kg), BMI(kg/m^2), cruris length(cm), and circumference(cm) for estimating tendon and graft size before surgery, differs between peroneus longus and semitendinosus autografts.
|
Preoperatively at surgery day
|
|
Predictability of Autograft Dimensions Based on Preoperative Anthropometric Data
Time Frame: Intraoperatively
|
To evaluate the predictive power of anthropometric variables (height(cm), weight(kg), BMI(kg/m^2), cruris length(cm), and circumference(cm)) for estimating tendon and graft size(cm) before surgery.
|
Intraoperatively
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 6, 2025
Primary Completion (Actual)
July 27, 2026
Study Completion (Actual)
July 27, 2026
Study Registration Dates
First Submitted
January 1, 2025
First Submitted That Met QC Criteria
January 7, 2025
First Posted (Actual)
January 10, 2025
Study Record Updates
Last Update Posted (Actual)
July 28, 2026
Last Update Submitted That Met QC Criteria
July 27, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 24237859611
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.