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NCT Number: NCT07753707

Influence of the Different Types of Tibial Fixation in the Reconstruction of the Anterior Cruciate Ligament of the Knee: Osseous Integration, Ligament Maturation and Clinical Results.

Influence of different tibial fixation methods in anterior cruciate ligament (ACL) reconstruction: bone integration, graft maturation, and clinical outcomes.

Primary Objective

To assess whether any of the four tibial fixation techniques is superior in terms of:

Graft-bone integration (CT/MRI),

Graft maturation (MRI),

Clinical outcomes (IKDC, Lysholm, Tegner scores; manual and instrumented knee stability with KT-1000 arthrometer).

Secondary Objectives

Compare clinical outcomes among groups (IKDC, Lysholm, Tegner).

Compare re-rupture rates and patient satisfaction.

Study Design

Prospective randomized trial.

The study will be registered in the international Clinical Trials registry.

Inclusion Criteria

Age ≥18 years.

Complete ACL rupture treated with arthroscopic ACL reconstruction using autologous hamstring tendons.

Exclusion Criteria

Age ≥55 years.

Patients treated with allografts, bone-patellar tendon-bone grafts, or quadriceps tendon grafts.

Malpositioned tunnels (evaluated by MRI at 6 months postop).

Previous knee surgery.

Femoral or tibial deformities.

Multiligament injuries.

Note: Soft tissue procedures (e.g., meniscal repair) are not exclusion criteria.

Randomization

Patients meeting inclusion/exclusion criteria will be randomized (via Research Randomizer: https://www.randomizer.org/

) into 3 groups:

Group A (TORN): bioabsorbable interference screw, same diameter as the tunnel.

Group B (TORN+1): bioabsorbable interference screw, one mm larger than the tunnel diameter.

Group C (TORN-BT): interference screw (same size as tunnel) + second fixation with cortical button/plate.

Sample size: 37 patients per group, 111 total.

Follow-up

Radiographic, CT, and MRI evaluation pre-op, at 15 days, and at 1 year post-op.

Clinical and radiological follow-up for 1 year.

Statistical Analysis

In the prospective phase, Student's t-test will be performed for comparison of pre- and postoperative variables. All variables will also be compared between groups and within groups (baseline vs. end of follow-up) using analysis of variance (ANOVA).

Linear regression models will be applied to test for potential significance that could be masked by confounding factors.

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This study is active but is not currently recruiting participants.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hospital Universitario Dexeus

Barcelona, BARCELONA, 08028, Spain

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Age ≥18 years.

Complete ACL rupture treated with arthroscopic ACL reconstruction using autologous hamstring tendons.

Exclusion criteria

Age ≥55 years.

Patients treated with allografts, bone-patellar tendon-bone grafts, or quadriceps tendon grafts.

Malpositioned tunnels (evaluated by MRI at 6 months postop).

Previous knee surgery.

Femoral or tibial deformities.

Multiligament injuries.

Note: Soft tissue procedures (e.g., meniscal repair) are not exclusion criteria.

Treatment and study plan

Anterior cruciate ligament (ACL) reconstruction

Procedure

The three different types of tibial fixation in ACL reconstruction with Hamstring autograft:

Group A (TORN): bioabsorbable interference screw, same diameter as the tunnel.

Group B (TORN+1): bioabsorbable interference screw, one mm larger than the tunnel diameter.

Group C (TORN-BT): interference screw (same size as tunnel) + second fixation with cortical button/plate.

Primary outcomes

  1. ACL Graft-bone integration (CT/MRI)

    Time frame: 12 months

    Graft-bone integration assessed by CT or MRI according to tunnel healing and bone incorporation.

  2. Graft maturation (MRI)

    Time frame: 6-12 months

    Graft maturation assessed on MRI using the Signal-to-Noise Quotient (SNQ).

Secondary outcomes

  1. International Knee Documentation Committee (IKDC) Subjective Knee Evaluation Score

    Time frame: 12 months

    Patient-reported knee function. Scores range from 0 to 100, with higher scores indicating better knee function.

  2. Tegner Activity Scale

    Time frame: 12 months

    Activity level assessed using the Tegner Activity Scale. Scores range from 0 to 10, with higher scores indicating higher activity levels.

  3. Side-to-side anterior knee laxity measured with KT-1000 arthrometer

    Time frame: 12 months

    Anterior tibial translation measured using a KT-1000 arthrometer. Lower side-to-side differences indicate better knee stability.

Sponsors and collaborators

Lead sponsor

Institut Català de Traumatologia i Medicina de l'Esport

Other

Registry information

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Aug 7, 2026
Registry last updated
Aug 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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