Predicting tendon size for ACL surgery based on body measurements
Anthropometric Predictability of Full-Thickness Peroneus Longus and Semitendinosus Autograft Size: A Comparative Analysis
This study is trying to see if body measurements like height and weight can help predict the right size of tendon needed for ACL surgery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 180 (estimated) |
| Ages | 18 Years to 45 Years |
| Sex | All |
| Sponsor | Karadeniz Technical University Academic / other |
| Locations | 1 site (Trabzon) |
| Trial ID | NCT06769724 on ClinicalTrials.gov |
What this trial studies
This observational study aims to explore the relationship between anthropometric variables, such as height, weight, and BMI, and the size of autografts used in anterior cruciate ligament (ACL) reconstruction. It will collect data on various preoperative parameters, including cruris length and circumference, as well as intraoperative details like tendon type and graft dimensions. By analyzing this data, the study seeks to establish a correlation that can help predict the appropriate tendon size needed for successful ACL surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 18-45 who have been diagnosed with an ACL rupture and are eligible for harvesting the semitendinosus or peroneus longus tendon.
Not a fit: Patients with a history of previous surgery on the donor side knee or ankle, congenital defects, or multiple ligament injuries may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to more personalized and effective ACL reconstruction surgeries by ensuring the right graft size is used.
How similar studies have performed: While this approach is based on established principles of graft selection, the specific correlation analysis of anthropometric variables with tendon size in ACL reconstruction is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Trabzon
- Karadeniz Technical University, Orthopedic and Traumatology Department — Trabzon, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Fevzi Gurkan Aslan, Medical Doctor
- Email: fevzigurkanaslan@yahoo.com
- Phone: +905377085171
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.