Anthropometric Predictability of Full-Thickness Peroneus Longus and Semitendinosus Autograft Size

March 17, 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

Recruiting

Conditions

Intervention / Treatment

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 (Estimated)

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 Contact

Study Locations

  • Turkey (Türkiye)
      • Trabzon, Turkey (Türkiye)
        • Recruiting
        • Karadeniz Technical University, Orthopedic and Traumatology Department
        • Contact:

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
Procedure: Anterior cruciate ligament reconstruction surgery
Anterior cruciate ligament reconstruction surgery with semitendinosus tendon autograft
Procedure: Anterior cruciate ligament reconstruction surgery
Anterior cruciate ligament reconstruction surgery with peroneus longus autograft
Peroneus Longus Tendon
The participiants underwent acl reconstruction with peroneus longus tendon autograft
Procedure: Anterior cruciate ligament reconstruction surgery
Anterior cruciate ligament reconstruction surgery with semitendinosus tendon autograft
Procedure: Anterior cruciate ligament reconstruction surgery
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

Karadeniz Technical University

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.

General Publications

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 (Estimated)

September 6, 2026

Study Completion (Estimated)

September 6, 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)

March 19, 2026

Last Update Submitted That Met QC Criteria

March 17, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Keywords

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.

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