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A Clinical Trial of the Round-tunnel and Flat-tunnel Technique of ACL Reconstruction

Primary Purpose

Anterior Cruciate Ligament Rupture

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
round tunnel technique
flat tunnel technique
Sponsored by
Peking University Third Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anterior Cruciate Ligament Rupture

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • For the first time, the knee joint simply ruptures the anterior cruciate ligament (ACL) and requires surgical reconstruction; it can be combined with meniscus injury, and the Outerbridge injury score is ≤ Grade II; There is no history of trauma or fracture of the ipsilateral knee joint; Posterior Cruciate Ligament (PCL) has no damage; Medial Collateral Ligament (MCL) or Lateral collateral ligaments (LCL) has no damage or only slight damage (no more than I degree).

Exclusion Criteria:

  • BMI is less than 18.5 or greater than 35 kg/m2; Patients with moderate or severe knee degeneration; Those with limited flexion angle (<120 degrees); The cartilage defect area is greater than 2 cm2 or the Outerbridge damage score is> Grade II.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Other

    Experimental

    Arm Label

    Control Group

    Experimental group

    Arm Description

    round tunnel

    flat tunnel

    Outcomes

    Primary Outcome Measures

    KT-2000
    side-to-side difference

    Secondary Outcome Measures

    Tegner Score
    functional scores
    Lysholm Score
    functional scores
    IKDC Score
    functional scores
    Lachman test
    physical examination
    Pivot-shift test
    physical examination

    Full Information

    First Posted
    June 27, 2021
    Last Updated
    June 27, 2021
    Sponsor
    Peking University Third Hospital
    Collaborators
    The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School, Zhengzhou Orthopaedic Hospital, Shenzhen Second People's Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04953676
    Brief Title
    A Clinical Trial of the Round-tunnel and Flat-tunnel Technique of ACL Reconstruction
    Official Title
    A Randomized, Controlled, Multi-center Clinical Trial of the Round-tunnel and Flat-tunnel Technique of Anterior Cruciate Ligament (ACL) Reconstruction
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2021
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 1, 2021 (Anticipated)
    Primary Completion Date
    September 1, 2022 (Anticipated)
    Study Completion Date
    September 1, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Peking University Third Hospital
    Collaborators
    The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School, Zhengzhou Orthopaedic Hospital, Shenzhen Second People's Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    This study intends to perform round-tunnel and flat-tunnel ACL reconstruction technique in 144 patients, and compare the clinical outcomes of the two surgical procedures through follow-up.
    Detailed Description
    This is a prospective randomized, controlled, multi-center clinical trial study on ACL reconstruction surgery technique. It is jointly undertaken by the Peking University Third Hospital, Nanjing Drum Tower Hospital, Zhengzhou Orthopaedic Hospital, and Shenzhen Second People's Hospital. Peking University Third Hospital is the team leader unit. In this study, 144 patients with ACL rupture were recruited according to the enrollment criteria. Among them, 54 patients with ACL rupture were recruited and carried out by the Peking University Third Hospital. The recruited patients were randomly divided into groups. The ratio of the control group is 1:1. Each of the other three hospitals recruited 30 patients and randomly grouped them according to the same enrollment criteria. The ratio of the experimental group to the control group was also 1:1. In this study, 72 patients with ACL rupture in the experimental group will be treated with flat-tunnel reconstruction technique, and 72 patients with ACL rupture in the control group will be treated with round-tunnel technique. All operations will be performed with autologous hamstring tendons. After reconstruction, all subjects will participate in the collection of clinical function scores including Tegner score, Lysholm score, IKDC score, and clinical evaluation including physical examination, joint laxity, CT and MRI imaging analysis to verify ACL Advantages of flat-tunnel technique.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Anterior Cruciate Ligament Rupture

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    144 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Control Group
    Arm Type
    Other
    Arm Description
    round tunnel
    Arm Title
    Experimental group
    Arm Type
    Experimental
    Arm Description
    flat tunnel
    Intervention Type
    Procedure
    Intervention Name(s)
    round tunnel technique
    Intervention Description
    Both the femoral tunnel and tibial tunnel were drilled by 8-mm cannulated drill
    Intervention Type
    Procedure
    Intervention Name(s)
    flat tunnel technique
    Intervention Description
    Both the femoral tunnel and tibial tunnel were dimension of 5×11-mm rounded-rectangular, which was created by initially drilling a round tunnel with a 5-mm cannulated drill and reshaped by use of a bone rasp and custom-made dilator.
    Primary Outcome Measure Information:
    Title
    KT-2000
    Description
    side-to-side difference
    Time Frame
    6 months, 12 months, 24 months
    Secondary Outcome Measure Information:
    Title
    Tegner Score
    Description
    functional scores
    Time Frame
    6 months, 12 months, 24 months
    Title
    Lysholm Score
    Description
    functional scores
    Time Frame
    6 months, 12 months, 24 months
    Title
    IKDC Score
    Description
    functional scores
    Time Frame
    6 months, 12 months, 24 months
    Title
    Lachman test
    Description
    physical examination
    Time Frame
    6 months, 12 months, 24 months
    Title
    Pivot-shift test
    Description
    physical examination
    Time Frame
    6 months, 12 months, 24 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    45 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: For the first time, the knee joint simply ruptures the anterior cruciate ligament (ACL) and requires surgical reconstruction; it can be combined with meniscus injury, and the Outerbridge injury score is ≤ Grade II; There is no history of trauma or fracture of the ipsilateral knee joint; Posterior Cruciate Ligament (PCL) has no damage; Medial Collateral Ligament (MCL) or Lateral collateral ligaments (LCL) has no damage or only slight damage (no more than I degree). Exclusion Criteria: BMI is less than 18.5 or greater than 35 kg/m2; Patients with moderate or severe knee degeneration; Those with limited flexion angle (<120 degrees); The cartilage defect area is greater than 2 cm2 or the Outerbridge damage score is> Grade II.

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    A Clinical Trial of the Round-tunnel and Flat-tunnel Technique of ACL Reconstruction

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