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
About this trial
This is an interventional treatment trial for Anterior Cruciate Ligament Rupture
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.
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
NCT ID
NCT04953676
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
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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