Correlation between where the knee tunnels are placed during ACL reconstruction and how well the knee heals
Official title: EVALUATION OF THE CORRELATION BETWEEN BONE TUNNEL PROJECTION PLACEMENT AND CLINICAL OUTCOMES IN ANTERIOR CRUCIATE LIGAMENT RECONSTRUCTION SURGERY
Run by Sakarya University · NCT07876635 · Data updated 2026-11-12
This study tests whether the position of the femoral and tibial tunnels during ACL reconstruction relates to how well patients recover.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 50 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Sakarya University Academic / other |
| Locations | 2 sites (Sakarya and 1 other locations) |
| Status | Recruiting |
| Started | June 1, 2026 |
| Main results expected | January 2, 2027 |
| Study ends | January 2, 2028 |
| Registry record updated | October 15, 2026 |
| Trial ID | NCT07876635 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–50 undergoing primary ACL reconstruction with available pre- and postoperative imaging and follow-up.
✕Probably not a fit
Patients without complete follow-up data or those with additional ligament injuries may not benefit from this study’s conclusions.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study will record surgical details from ACL reconstructions, including tunnel placement and graft characteristics, and relate them to postoperative outcomes. Preoperative knee instability and side-to-side laxity will be measured with objective tools, while postoperative recovery will be tracked using Lysholm and IKDC scores, plus timelines for returning to daily activities and sports. Imaging data (CT/MRI/radiographs) and intraoperative variables will be analyzed to explore associations with clinical and functional results over at least 6 months of follow-up.
Why it matters
Potential benefit: If successful, the findings could help surgeons optimize tunnel placement to improve recovery and function after ACL reconstruction.
How similar studies have gone: Previous research has explored tunnel placement with mixed results, making this observational evaluation a meaningful contribution to the field.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: Patients aged 18-50 years. Patients diagnosed with unilateral anterior cruciate ligament (ACL) injury. Patients scheduled to undergo primary ACL reconstruction. Patients who are willing and able to complete a postoperative follow-up period of at least 6 months. Patients with available postoperative radiological assessments, including computed tomography (CT), magnetic resonance imaging (MRI), and/or standard radiographs, as required by the study protocol. Patients with clinical outcome assessments, including the Lysholm Knee Score and International Knee Documentation Committee (IKDC) score, recorded during the planned follow-up period. Exclusion Criteria: Patients with multiligament knee injuries, including clinically significant concomitant posterior cruciate ligament (PCL), medial collateral ligament (MCL), or lateral collateral ligament (LCL) injuries. Patients with a history of previous non-ACL surgery on the affected knee. Patients with advanced knee osteoarthritis. Patients who develop a postoperative infection. Patients with insufficient or inadequate radiological imaging data for the planned assessments. Patients who do not complete at least 6 months of postoperative follow-up. Patients with neuromuscular disorders or systemic connective tissue diseases. Patients with incomplete or inadequately recorded clinical outcome scores.
Where it's running
-
Sakarya Üniversitesi Eğitim Ve Araştirma Hastanesi
Sakarya, Turkey (Türkiye) Recruiting -
Sakarya Üniversitesi Eğitim Ve Araştirma Hastanesi
Sakarya, Turkey (Türkiye) Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.