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Bone Tunnel Widening Following ACL Reconstruction

Primary Purpose

Anterior Cruciate Ligament Injury, Knee Injuries

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Surgical reconstruction of the ACL
Sponsored by
Hospital for Special Surgery, New York
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anterior Cruciate Ligament Injury focused on measuring ACL, Tunnel, Widening

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Individuals within the age range of 18 to 55 years who are diagnosed with anterior cruciate insufficiency and have decided to undergo ACL reconstruction using autogenous graft will be included in the study. Exclusion Criteria: Individuals that have previous knee surgeries, multi-ligament injuries, systemic ligament disorders such as Ehlers Danlos syndrome or connective tissue disorders will be excluded from the study. Individuals who are pregnant or expect to be pregnant during the course of the study or who are especially concerned with X-ray exposure should also be excluded.

Sites / Locations

  • Hospital for Special Surgery

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Surgical Reconstruction of the ACL

Arm Description

Outcomes

Primary Outcome Measures

Bone Tunnel Diameter
Bone tunnel diameter measured on MRI

Secondary Outcome Measures

Full Information

First Posted
September 13, 2005
Last Updated
May 16, 2017
Sponsor
Hospital for Special Surgery, New York
Collaborators
Inion Oy
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1. Study Identification

Unique Protocol Identification Number
NCT00198042
Brief Title
Bone Tunnel Widening Following ACL Reconstruction
Official Title
Bone Tunnel Widening Following ACL Reconstruction
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
June 2004 (undefined)
Primary Completion Date
December 31, 2015 (Actual)
Study Completion Date
December 31, 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital for Special Surgery, New York
Collaborators
Inion Oy

4. Oversight

5. Study Description

Brief Summary
Hypothesis 1: There is less tunnel-widening with bone-patella tendon-bone graft compared with the hamstring graft when the same fixation method is used. Tunnel widening is greater with achilles tendon allografts versus autograft bone-patella tendon-bone and hamstring autografts. Hypothesis 2: Tunnel widening occurs in the early post-operative period (< 8 weeks) when the tendon remodels within the bone tunnels. Hypothesis 3: Low pre-operative bone mineral density is associated with tunnel widening.
Detailed Description
This will be a prospective study for patients undergoing ACL reconstruction using bone-patella tendon-bone graft, hamstring graft or achilles allograft. Each group will have ACL reconstruction with fixation using bioabsorbable interference screws on the femoral and tibial side. Patients will be evaluated on the day of surgery, 6, 12, 24, 52 and 104 weeks post-operatively. Evaluations will include pre-operative regional and standard bone mineral density measurements, post-operative MRI evaluation of tunnel dimensions and bone-tendon interface, radiographic evaluation of tunnel dimensions and routine clinical follow-up. Interventions or Observations - outline specific procedures, treatments and/or interventions, as well as sources of research material to be utilized, which will involve human subjects or human materials that will be part of this research project. This study will require a pre-operative bone mineral density measurement in the Nuclear Medicine Division of the Department of Radiology at HSS. Standard measurements of the femoral neck, spine as well as regional studies of the distal femur and proximal tibia of the injured knee will be performed. On the day of surgery, the patient will undergo ACL reconstruction using bioabsorbable interference screw fixation of the hamstring, bone-patella tendon-bone graft, or achilles allograft. This is a standard procedure. The choice of graft type (hamstring, bone-patella tendon-bone graft, or achilles allograft) will be discussed with the patients and the patient will decide graft type pre-operatively. In this study, we will standardize the fixation method by using bioabsorbable interference screws. Post-operatively, the patient will undergo a limited MRI scan to evaluate the tunnel dimensions as well as graft placement prior to discharge from the hospital. During the patients' 6 weeks, 12 weeks and 24 weeks clinical follow-up, they will be evaluated by their orthopaedic surgeon for clinical progress. Standard radiographs will be obtained of the patient's knee at the 6 weeks and 24 weeks follow-up visit. These are standard radiographic evaluations and are of no additional charge to the patients. We will utilize these images for radiographic measurements of tunnel expansion. During these visits, the patients will also undergo limited MRI scan of the femoral tunnel and tibia tunnel. With the serial MRI images, we will be able to make accurate measurements of the femoral and tibial tunnels. In addition, we will be able to evaluate the bone-tendon interface as well as the maturation of the intra-articular portion of the ACL graft. At 24, 52 and 104 weeks the patients will also be given standard IKDC and Lysholm clinical knee outcome questionnaires and will have objective stability measurements of both the operative and non-operative knees using a KT-1000 instrument. Overall Study Protocol: Pre-operative work-up 1. Bone mineral density measurement by D.E.X.A. Day of Surgery: ACL reconstruction using bioabsorbable interference screws Limited CT scans to quantitate tunnel dimensions 6 weeks post-operatively Regular clinical follow-up Regular plain radiographs to quantitate tunnel dimensions Limited MRI scans to quantitate tunnel dimensions 12 weeks post-operatively Regular clinical follow-up Limited MRI scans to quantitate tunnel dimensions 24 weeks post-operatively Regular clinical follow-up and KT-1000 measurements Regular plain radiographs to quantitate tunnel dimensions MRI study to evaluate tendon-bone interface, graft maturation, tunnel dimensions and trabecular remodeling Patients will answer IKDC and Lysholm knee questionnaires 52 weeks post-operatively Regular clinical follow-up and KT-1000 measurements Patients will answer IKDC and Lysholm knee questionnaires Limited MRI 104 weeks post-operatively Regular clinical follow-up and KT-1000 measurements Patients will answer IKDC and Lysholm knee questionnaires Limited MRI Number of Subjects (power justification for numbers) A power analysis was performed to determine the number of subjects needed to determine significance between the hamstring and bone-patella tendon-bone group. Data from previous studies demonstrate tunnel widening up to 77 ± 28% following ACL reconstruction using hamstring tendons. We estimate that a 30% decrease in this amount of tunnel widening would be clinically significant. This extrapolates to a 54% increase in tunnel dimensions. Using these estimations, a power of 0.80 with α = 0.5 is achieved using 20 subjects per group (BPTB versus hamstring).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anterior Cruciate Ligament Injury, Knee Injuries
Keywords
ACL, Tunnel, Widening

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
18 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Surgical Reconstruction of the ACL
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Surgical reconstruction of the ACL
Intervention Description
Surgical reconstruction of the ACL
Primary Outcome Measure Information:
Title
Bone Tunnel Diameter
Description
Bone tunnel diameter measured on MRI
Time Frame
2 years
Other Pre-specified Outcome Measures:
Title
Bone Tunnel Cross Sectional Area
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Individuals within the age range of 18 to 55 years who are diagnosed with anterior cruciate insufficiency and have decided to undergo ACL reconstruction using autogenous graft will be included in the study. Exclusion Criteria: Individuals that have previous knee surgeries, multi-ligament injuries, systemic ligament disorders such as Ehlers Danlos syndrome or connective tissue disorders will be excluded from the study. Individuals who are pregnant or expect to be pregnant during the course of the study or who are especially concerned with X-ray exposure should also be excluded.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Scott Rodeo, MD
Organizational Affiliation
Hospital for Special Surgery, New York
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital for Special Surgery
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States

12. IPD Sharing Statement

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Bone Tunnel Widening Following ACL Reconstruction

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