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Clinical Trial Comparing Three Anterior Cruciate Ligament Reconstructive Procedures

Primary Purpose

Knee Injuries

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Single bundle hamstring
Double bundle hamstring
Bone patellar tendon bone
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Injuries focused on measuring Anterior cruciate ligament rupture, Anterior cruciate ligament(A02.513.514.100)

Eligibility Criteria

18 Years - 40 Years (Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Men above age 18-40 years old
  • First ACL reconstruction surgery
  • Single leg involvement

Exclusion Criteria:

  • ACL injury less than 6 weeks as deleterious effect of the injury may affect the extension range
  • Injury on Duty (IOD) cases
  • Other associated injuries (Fractures, other ligaments involvement, neurovascular bundles injury),Chondral lesion with co-commitment intervention
  • Concomitant meniscus repair in same operation, or within 3 months before the operation
  • Significant OA changes
  • Known chronic disease or receiving long term medications affecting bone metabolism, including anabolic steroids, medication for thyroid hormone therapy or osteoporosis
  • Neurological deficit

Sites / Locations

  • Prince of Wales Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Single bundle hamstring

Double bundle hamstring

Bone patellar tendon bone

Arm Description

Outcomes

Primary Outcome Measures

International Knee Documentation Committee (IKDC)Knee Form 2000 Score
It is a score on a scale from 0 to 100. It is a knee-specific measure of symptoms, function and sports activity of subjects based on self-report. 0 represents the worst while 100 represents the best score. The higher the score, the better the knee function.

Secondary Outcome Measures

Percentage Distal Femoral Bone Mineral Density (BMD)Decrease
% BMD decrease of distal femur of injured side with reference to the BMD at day 1 after surgery

Full Information

First Posted
January 4, 2007
Last Updated
March 22, 2012
Sponsor
Chinese University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT00418964
Brief Title
Clinical Trial Comparing Three Anterior Cruciate Ligament Reconstructive Procedures
Official Title
Functional, Clinical & Radiological Outcome of Anterior Cruciate Ligament Reconstruction: A Prospective Randomized Control Clinical Trial Studies Comparing Bone Patella Bone, Single Bundle and Double Bundle Method.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2012
Overall Recruitment Status
Completed
Study Start Date
December 2006 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
June 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of this prospective study is to assess the clinical, functional and radiological outcomes of three different ACL reconstruction procedures: Bone Patella Bone graft, Single bundle hamstring graft and anatomical Double bundle graft in terms of pain, swelling, mobility, quadriceps girth size, stability, proprioception, bone mineral density and functional status.
Detailed Description
Anterior cruciate ligament (ACL) reconstruction surgery is one of the common procedures performed by orthopedic surgeons with approximately 100,000 cases performed per year in the United States. A large amount of sports injuries were related to ACL problem. As such, ACL injuries and treatment is still widely under intensive study. Traditionally, ACL surgery has been focused on using bone patella bone graft and single bundle hamstring graft. Problems of knee pain, unstable fixation, rotational instability and degenerative changes were reported. Recently, the use of double bundle hamstring graft to reconstruct the ACL according its anatomy aiming to improve the rotational stability was proposed. However, results about the clinical, functional and radiological outcomes are limited. The objective of this prospective pilot study is to assess the clinical, functional and radiological outcomes of three different ACL reconstruction procedures: Bone Patella Bone graft, Single bundle hamstring graft and anatomical Double bundle graft in terms of pain, swelling, mobility, quadriceps girth size, stability, proprioception, skin sensation, bone mineral density and functional status. Subjects to be operated for ACL reconstruction and meeting the inclusion and exclusion criteria will be recruited. Subjects will be randomly assigned to the three surgical groups by block randomization. Demographic information, parameters in recovery domain, functional domain and stability domain, isokinetic test, motion analysis domain, proprioception and radiographical measurements will be made at baseline and at day 1, week 2, week 4, week 8, month 3, month 5, 1 year and 2 years post-surgery. The effect of different surgical techniques and time on the different outcomes will be analysed by 2-way ANOVA.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Injuries
Keywords
Anterior cruciate ligament rupture, Anterior cruciate ligament(A02.513.514.100)

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
62 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Single bundle hamstring
Arm Type
Experimental
Arm Title
Double bundle hamstring
Arm Type
Experimental
Arm Title
Bone patellar tendon bone
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Single bundle hamstring
Intervention Description
Single bundle hamstring
Intervention Type
Procedure
Intervention Name(s)
Double bundle hamstring
Intervention Description
Double bundle hamstring
Intervention Type
Procedure
Intervention Name(s)
Bone patellar tendon bone
Intervention Description
Bone patellar tendon bone
Primary Outcome Measure Information:
Title
International Knee Documentation Committee (IKDC)Knee Form 2000 Score
Description
It is a score on a scale from 0 to 100. It is a knee-specific measure of symptoms, function and sports activity of subjects based on self-report. 0 represents the worst while 100 represents the best score. The higher the score, the better the knee function.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Percentage Distal Femoral Bone Mineral Density (BMD)Decrease
Description
% BMD decrease of distal femur of injured side with reference to the BMD at day 1 after surgery
Time Frame
1 year

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men above age 18-40 years old First ACL reconstruction surgery Single leg involvement Exclusion Criteria: ACL injury less than 6 weeks as deleterious effect of the injury may affect the extension range Injury on Duty (IOD) cases Other associated injuries (Fractures, other ligaments involvement, neurovascular bundles injury),Chondral lesion with co-commitment intervention Concomitant meniscus repair in same operation, or within 3 months before the operation Significant OA changes Known chronic disease or receiving long term medications affecting bone metabolism, including anabolic steroids, medication for thyroid hormone therapy or osteoporosis Neurological deficit
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kai Ming Chan
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prince of Wales Hospital
City
Hong Kong SAR
Country
China

12. IPD Sharing Statement

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Clinical Trial Comparing Three Anterior Cruciate Ligament Reconstructive Procedures

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