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Single and Double Bundle ACL Reconstructions, in Term of Cartilage Damage Due to Remaining Instability After Surgery. (ACL)

Primary Purpose

Anterior Cruciate Ligament Rupture, Knee Instability, Cartilage Damage

Status
Unknown status
Phase
Not Applicable
Locations
Indonesia
Study Type
Interventional
Intervention
Single Bundle ACL Reconstruction
Double Bundle ACL Reconstruction
Sponsored by
Indonesia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anterior Cruciate Ligament Rupture focused on measuring knee instability, anterior cruciate ligament rupture, cartilage damage, Single Bundle ACL Reconstruction, Double Bundle ACL Reconstruction, COMP (Cartilage Oligomeric Matrix Protein), MRI T2 Mapping

Eligibility Criteria

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

Inclusion Criteria:

  • Male
  • Age 18-40 years
  • Total primary ACL rupture
  • Injury time 1-12 months
  • Willingness to attend the study
  • Signed informed consent.

Exclusion Criteria:

  • Subjects having other ligament injuries in the knee
  • History of rheumatoid arthritis
  • Severe osteoarthritis Kellgren-Lawrence grading> 2
  • Body Mass Index (BMI) ≥ 25
  • Fracture around the knee joint or osteochondral avulsion
  • History of injury with either or both semitendinosus or gracilis muscle, patellofemoral instability, contraindication of anesthesia, and partial ACL rupture.

Sites / Locations

  • Fakultas Kedokteran Universitas IndonesiaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Synovial fluid COMP

MRI T2 Mapping

Instability Examination

Arm Description

Knee joint fluid is aspirated for ELISA COMP examination

Affected knee is subjected to an MRI T2 mapping examination to see the condition of cartilage

Lachmant Test, Pivot shift test and Rolimeter Measurement

Outcomes

Primary Outcome Measures

Changes of Synovial fluid Cartilage Oligomeric Matrix Protein (sfCOMP) Concentration from Baseline to 3 months and 6 months
Sample will be taken from Synovial fluid and and send to laboratory for checking the concentration (ng/mL) of COMP using ELISA (enzyme-linked immunosorbent assay) kits.
Changes of MRI T2 Mapping colour from Baseline to 3 months and 6 months
The cartilage of the affected knee will be checked using MRI T2 Mapping and the resulting color will be quantitatively assessed in seconds.
Changes of Lachman test score from baseline to 3 months and 6 months
Anterior instability on the affected knee will be checked using the Lachman test and the score is recorded in millimeter (mm).
Changes of Pivot shift test score from baseline to 3 months and 6 months
Rotatory instability on the affected knee will be checked using the Pivot shift test and the score is recorded in +1, +2, +3.
Changes of Rolimeter measurement score from baseline to 3 months and 6 months
Anterior instability on the affected knee will be checked using the Rolimeter tools and the measurement is recorded in millimeter (mm).

Secondary Outcome Measures

Full Information

First Posted
October 22, 2020
Last Updated
November 8, 2020
Sponsor
Indonesia University
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1. Study Identification

Unique Protocol Identification Number
NCT04626999
Brief Title
Single and Double Bundle ACL Reconstructions, in Term of Cartilage Damage Due to Remaining Instability After Surgery.
Acronym
ACL
Official Title
Effect of Knee Instability Due To Rupture Of Anterior Cruciate Ligament On Cartilage Damage Related To Types of Reconstruction Therapy: In Biomechanic, Biomolecular and Radiological Aspects
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 8, 2018 (Actual)
Primary Completion Date
June 2021 (Anticipated)
Study Completion Date
June 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indonesia University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The prevalence of ACL (Anterior Cruciate Ligament) ruptures is relatively high, primarily due to sports and military training injuries. With the advancements of ACL reconstruction therapies, there exist two ways to reconstruct ACL: single-bundle ACL reconstruction (SBACLR) and double-bundle ACL reconstruction (DBACLR). Previous research studies claimed that DBACLR techniques are superior to that of SBACLR, while others stated no notable differences between the two. The variables assessed in previous studies are findings related to the clinical instabilities of the knees (both subjective nor objectives views) and standard radiology examination, such as Xray or MRI. Knee instabilities are the primary goal of ACL reconstructions. Hence this study focuses on finding the dissimilarities between the two previously mentioned techniques by observing the early consequences (subclinically) of knee instabilities towards cartilage damage. The dissimilarities assessments utilize biomolecular tests (ELISA) of cartilage oligomeric matrix protein (COMP) on synovial joint fluid of the knee and knee joint cartilage examination using MRI T2 mapping. Furthermore, there will be a stability (biomechanical) check of the knee joint in the form of a Lachman test, a pivot shift test, and a Rolimeter. This study requires around 47-52 subjects divided into two operation techniques of SBACLR and DBACLR. To evaluate the results from COMP, MRI T2 mapping, Lachman test, pivot shift test, and Rolimeter, this study is divided into three timeframes: before an operation, three months after post-operation, and six months post-operations. The differences between the test variables are then used as an indicator to assess the cartilage conditions from two operation techniques: SBACLR and DBACLR. Subsequently, the study also examines the possible correlation of each of the resulting variables.
Detailed Description
This study utilizes a single-blind randomized clinical trial to evaluate whether the DBACL reconstruction surgery is more suitable than SBACL reconstruction in the subclinical aspect of cartilage damage through a biomolecular examination from the synovial joint fluid COMP and MRI T2 mapping. This study's estimated time is between two to three years ranging from January 2018 until the end of June 2021. The samples are randomly divided into two groups: the SBACLR group and the DBACLR group. The sample size for each group was 26 subjects. For the subjects, the accepted inclusion criteria were male, age 18-40 years, total primary AC rupture, injury time 1-12 months, willingness to attend the study, and signed informed consent. Exclusion criteria include subjects having other ligament injuries in the knee, history of rheumatoid arthritis, severe osteoarthritis Kellgren-Lawrence grading> 2, Body Mass Index (BMI) ≥ 25, fracture around the knee joint or osteochondral avulsion, history of injury with either or both semitendinosus or gracilis muscle, patellofemoral instability, contraindication of anesthesia, and partial ACL rupture. Drop Out criteria includes: subjects not returning to control, undergoing treatment outside the program, not complying with study protocols, re-injury to the studied knee causing ligament, meniscus or cartilage injury, and postoperative knee infection. Prospective subjects have been diagnosed with the total loss of ACL and meet the research criteria are explained about the aims and objectives of the study and sign a consent form to participate in the study. Each subject was assigned to one of the study groups through a simple randomization method: the SBACL reconstruction surgery action group or the DBACL reconstruction surgery action group. All subjects were examined the Lachman test, pivot test, Rolimeter measurement, MRI T2 mapping, and knee joint fluid for ELISA examination of sfCOMP (synovial fluid COMP) at the time before surgery, the third month, and the sixth month postoperatively.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anterior Cruciate Ligament Rupture, Knee Instability, Cartilage Damage
Keywords
knee instability, anterior cruciate ligament rupture, cartilage damage, Single Bundle ACL Reconstruction, Double Bundle ACL Reconstruction, COMP (Cartilage Oligomeric Matrix Protein), MRI T2 Mapping

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
52 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Synovial fluid COMP
Arm Type
Active Comparator
Arm Description
Knee joint fluid is aspirated for ELISA COMP examination
Arm Title
MRI T2 Mapping
Arm Type
Active Comparator
Arm Description
Affected knee is subjected to an MRI T2 mapping examination to see the condition of cartilage
Arm Title
Instability Examination
Arm Type
Active Comparator
Arm Description
Lachmant Test, Pivot shift test and Rolimeter Measurement
Intervention Type
Procedure
Intervention Name(s)
Single Bundle ACL Reconstruction
Intervention Description
Arthroscopy Single Bundle ACL Reconstruction is a procedure to reconstruct the ACL using one bundle. The procedure uses Hamstring (Gracillis muscle and Semitendinosus muscle) as a graft.
Intervention Type
Procedure
Intervention Name(s)
Double Bundle ACL Reconstruction
Intervention Description
Arthroscopy Double Bundle ACL Reconstruction is a procedure to reconstruct the ACL using Two bundles (Double bundle). The procedure uses Gracillis tendon as a Posterolateral bundle graft and Semitendinosus tendon as an Anteromedial bundle graft.
Primary Outcome Measure Information:
Title
Changes of Synovial fluid Cartilage Oligomeric Matrix Protein (sfCOMP) Concentration from Baseline to 3 months and 6 months
Description
Sample will be taken from Synovial fluid and and send to laboratory for checking the concentration (ng/mL) of COMP using ELISA (enzyme-linked immunosorbent assay) kits.
Time Frame
0,3,6 months
Title
Changes of MRI T2 Mapping colour from Baseline to 3 months and 6 months
Description
The cartilage of the affected knee will be checked using MRI T2 Mapping and the resulting color will be quantitatively assessed in seconds.
Time Frame
0,3,6 months
Title
Changes of Lachman test score from baseline to 3 months and 6 months
Description
Anterior instability on the affected knee will be checked using the Lachman test and the score is recorded in millimeter (mm).
Time Frame
0,3,6 months
Title
Changes of Pivot shift test score from baseline to 3 months and 6 months
Description
Rotatory instability on the affected knee will be checked using the Pivot shift test and the score is recorded in +1, +2, +3.
Time Frame
0,3,6 months
Title
Changes of Rolimeter measurement score from baseline to 3 months and 6 months
Description
Anterior instability on the affected knee will be checked using the Rolimeter tools and the measurement is recorded in millimeter (mm).
Time Frame
0,3,6 months

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: Male Age 18-40 years Total primary ACL rupture Injury time 1-12 months Willingness to attend the study Signed informed consent. Exclusion Criteria: Subjects having other ligament injuries in the knee History of rheumatoid arthritis Severe osteoarthritis Kellgren-Lawrence grading> 2 Body Mass Index (BMI) ≥ 25 Fracture around the knee joint or osteochondral avulsion History of injury with either or both semitendinosus or gracilis muscle, patellofemoral instability, contraindication of anesthesia, and partial ACL rupture.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bobby N Nelwan
Phone
+62811898464
Email
bobbynelwan@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ismail H Dilogo, MD, PhD
Email
ismailortho@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bobby N Nelwan, MD
Organizational Affiliation
Fakultas Kedokteran Universitas Indonesia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fakultas Kedokteran Universitas Indonesia
City
Jakarta Pusat
State/Province
DKI Jakarta
ZIP/Postal Code
10430
Country
Indonesia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bobby N Nelwan, MD
Phone
+62811898464
Email
bobbynelwan@gmail.com
First Name & Middle Initial & Last Name & Degree
Aryo N Triyudanto, MD
Phone
+628119629571
Email
nugroho.triyudanto@gmail.com

12. IPD Sharing Statement

Learn more about this trial

Single and Double Bundle ACL Reconstructions, in Term of Cartilage Damage Due to Remaining Instability After Surgery.

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