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Meniscus TearNCT01931735

Prospective Trial of Arthroscopic Meniscectomy for Degenerative Meniscus Tears

A study testing Randomized Meniscectomy and Randomized Lavage in people with Meniscus Tear, run by VA Office of Research and Development at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Arthroscopic meniscectomy is among the most commonly performed orthopedic surgical procedures in the VA system. There remains substantial uncertainty, however, regarding the short term benefits and the long term consequences of arthroscopic meniscectomy in patients with degenerative meniscus tears. Read more about this study

Who is it for?
Ages 45 to 70 years
Conditions the study is for
Meniscus Tear
What is being tested?
Randomized Meniscectomy and Randomized Lavage
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
27 participants
Where
1 siteUnited States
Study dates
1 Oct 2013to 31 Jan 2018
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 45 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Veteran
  • Age between 45 and 70 years
  • Degenerative meniscus tear as seen on standard clinical MRI scan
  • Complaint of "mechanical symptoms" which would include popping, catching, or locking of the knee
  • Persistent symptoms for a minimum of three months despite conservative management
  • Patient is enrolled for arthroscopic meniscectomy
  • Subject agrees to the study follow-up schedule and signs informed consent.

Who cannot join

  • Radiographic osteoarthritis of the knee in any compartment greater than KL grade 2
  • Prior knee arthroscopy within two years of study enrollment
  • Unable to have an MRI scan
  • Does not agree to participate

Trial locations and contacts

1 site in 1 country.

United States1 site
  • VA Palo Alto Health Care System, Palo Alto, CA

    Palo Alto, California, 94304-1290

Other trials in United States

About this study

Arthroscopic meniscectomy is among the most commonly performed orthopedic surgical procedures in the VA system. There remains substantial uncertainty, however, regarding the short term benefits and the long term consequences of arthroscopic meniscectomy in patients with degenerative meniscus tears. Of major concern is the fact that degenerative meniscus tears are associated with osteoarthritis, and it is known that within two years of surgery, arthroscopic debridement for osteoarthritis is no better than placebo in relieving pain and restoring function. Longer term, meniscectomy has been shown to be associated with elevated risk of osteoarthritis development, raising the concern that meniscectomy can actually be harmful. The purpose of this study is to determine whether meniscectomy in the setting of a degenerative meniscus tear is of any clinical value. Determining this would either justify the expenses associated with arthroscopic meniscectomy on a large number of patients, or would identify an area of significant potential cost savings.

Read the detailed description

The overall goal of this project is to determine whether arthroscopic meniscectomy in degenerative meniscal tears is beneficial from a clinical and scientific viewpoint relative to a non-meniscectomy arthroscopy control. Arthroscopic meniscectomy is among the most commonly performed orthopedic surgical procedures in the VA system and nationally. In the investigators' practice at the VA Palo Alto Healthcare System over the last year, 80% of patients having knee arthroscopy for meniscus tears have been in the 45-70 years age group and 53% of these patients had degenerative meniscal tears without a large unstable flap. these data are comparable to arthroscopic meniscectomy data drawn in other settings. While meniscectomy is a common procedure there remains substantial uncertainty regarding the short term benefits and the long term consequences of arthroscopic meniscectomy in patients with degenerative meniscus tears. Of major concern is the fact that degenerative meniscus tears are associated with osteoarthritis, and it is known that within two years of surgery, arthroscopic debridement for osteoarthritis is no better than placebo in relieving pain and restoring function. Longer term, meniscectomy has been shown to be associated with elevated risk of osteoarthritis development, raising the concern that meniscectomy can actually be harmful. It has also been shown by the group that patients with clinically successful arthroscopic posterior medial meniscectomy have significant change in the rotational motion of the knee during walking. Rotational changes at the knee follow soft tissue damage and have been implicated in the causes for cartilage degeneration.

Thus, there are critical unanswered questions regarding the clinical benefit as well as the scientific basis for arthroscopic meniscectomy for degenerative meniscal tear. To address these questions, this project will conduct a prospective, randomized, blinded, and controlled study of arthroscopic meniscectomy in patients between the ages of 45 and 70 with stable degenerative meniscus tears. In this study, the control group will be a group of patients having arthroscopic lavage of the joint, but no debridement of the stable degenerative meniscus tear. The aims will address clinical (self-reported) and scientific (functional) outcomes of arthroscopic meniscectomy in the time frame lasting up to two years after surgery.

Aim 1: Test the clinical benefit of arthroscopic meniscectomy in the setting of a stable degenerative meniscus tear.

Hypothesis 1a: There will be a significant differences in WOMAC scores between the meniscectomy and the non-meniscectomy/lavage groups at 12 months following surgery.

Hypothesis 1b: The WOMAC scores of the non-meniscectomy/lavage group will not be inferior to the WOMAC scores of the meniscectomy group at 12 months after surgery.

Aim 2: To test the functional effect of arthroscopic meniscectomy in the setting of a degenerative meniscus tear.

Hypothesis 2: Subjects randomized to arthroscopy and meniscectomy will have greater changes in tibio-femoral rotation, knee adduction moment, and knee flexion moment at 12 months following surgery when compared to subjects randomized to arthroscopy and lavage.

In addition to the above principal aims of the study, the investigators will also pursue other exploratory aims:

  1. Understand whether arthroscopic meniscectomy for degenerative tear results in accelerated radiographic progression of osteoarthritis (KL score) and regional cartilage thinning (3D MRI thickness maps) relative to a control group.
  2. Understand whether tibio-femoral position changes measured in the investigators' gait analysis relate to radiographic progression of osteoarthritis and regional cartilage thinning relative to the control group.
  3. Understand whether meniscal tears are associated with activation of the complement system and alteration of gene expression in the synovial lining of the knee, and whether elevated complement activity relates to radiographic OA progression following surgery.
  4. Understand whether serum biomarkers are affected in degenerative meniscus tears and whether they will relate to radiographic OA progression or MRI changes following surgery.
  5. Investigate whether articular cartilage matrix changes that are measured by advanced MR techniques such as T1rho, sodium, or diffusion MRI can be identified and related to radiographic OA progression or MRI changes following surgery.

This prospective clinical trial with coordinated, multi-disciplinary approach will provide an important clinical and scientific assessment of arthroscopic meniscectomy. It will identify whether surgical treatment is efficacious, an important issue given the costs and risks of surgery. It will also provide new insight into incipient arthritis, yielding information that will impact future patient care.

Update 12/2/2015:

Since the grant was awarded, there has been a growing body of literature published that is directly applicable to the subject of the grant. Specifically, a prospective, randomized study was published in the New England Journal of Medicine in Dec 2013. In that study, the authors did what was proposed in the present study. They found that there was no benefit to meniscectomy in the setting of a degenerative meniscus tear in patients with minimal arthritis of the knee. A very similar study was published a few months before in one of the most important orthopedic journals that focuses on arthroscopy, the American Journal of Sports Medicine. That study was also a prospective randomized study and compared arthroscopic meniscectomy to non-operative treatment for degenerative meniscus tears. The authors of that study also found that arthroscopic meniscectomy for degenerative meniscus tears was of no benefit, this time over non-operative treatment.

When the study was conceived and when the study was funded, there was a genuine uncertainty regarding the appropriate treatment for patients with minimal to no arthritis and a degenerative meniscus tear. With this growing body of literature, however, there is more clarity on this question, and from an ethical standpoint, without genuine equipoise, discussing treatment options and recruiting patients into the study become problematic. The study design was then changed to a prospective observational study of patients with meniscus tears undergoing arthroscopic meniscectomy. The investigators will still be collecting the same data as in the prior randomized trial. The data are patient reported outcome questionnaires, MRI's, and gait analyses at time points from preoperative to two years postoperative. The investigators will also be collecting tissue samples at the time of surgery for the evaluation of inflammatory markers.

Since that time the investigators have reformulated hypotheses. Current aims and hypotheses are:

Aim 1: Determine whether TEAR PATTERN affects PATIENT REPORTED OUTCOMES of arthroscopic meniscectomy Hypothesis 1: There will be greater improvement in patient reported outcomes (WOMET) in patients with displacable meniscus tears than non-displacable meniscus tears.

Aim 2: Determine if STANDARD PREOPERATIVE MR IMAGING can predict PATIENT REPORTED OUTCOME following arthroscopic meniscectomy Hypothesis 2: Patients with MRI evident vertical tears involving 50% of the meniscus or patients with displaced meniscal flaps will have greater improvement in WOMET scores after debridement than those without these MRI findings.

Aim 3: Determine if TEAR PATTERN (and resulting debridement) affects GAIT CHARACTERISTICS at the knee at 12 months post debridement Hypothesis 3: Subjects having debridement of a medial meniscus root tear or a tear that extends through the entire medial meniscus to the periphery will have greater adduction moment and tibial external rotation, and lower flexion angle range of motion than patients who have retention of circumferential fiber continuity or a lateral tear.

Aim 4a: Determine if INFLAMMATORY MARKERS in the synovium at the time of surgery relate to PREOPERATIVE PAIN and PREOPERATIVE MENISCAL TEAR PATTERN.

Hypothesis 4a: Greater inflammation in the synovium will be correlated with greater preoperative pain and with more severe preoperative meniscal damage.

Aim 4b: Determine if INFLAMMATORY MARKERS in the synovium at the time of surgery relate to PATIENT REPORTED OUTCOME following arthroscopic meniscectomy.

Hypothesis 4b: Greater inflammation in the synovium at the time of surgery will be related to greater improvement in pain at three months following surgery.

Aim 5:Determine if PREOPERATIVE GAIT CHARACTERISTICS (knee flexion moment, knee adduction moment, and knee flexion angle) are related to preoperative WOMET scores Hypothesis 5: There will be a negative relationship between WOMET score and knee flexion moment preoperatively.

In addition to the above aims, the investigators will continue to pursue the exploratory aims that were described in the grant application. These are exploratory because they relate to osteoarthritis progression, an outcome that may not be measurable at the one year time frame. The exploratory aims and hypotheses are:

Exploratory Aim 1: Determine if TEAR PATTERN (and subsequent debridement) influences rate of osteoarthritis progression as measured by articular cartilage thinning at 2 years.

Exploratory Hypothesis 1: Tear patterns that involve the meniscal root or complete disruption of the circumferential fibers of the meniscus will exhibit more rapid progression of osteoarthritis than other tear patterns.

Exploratory Aim 2: Determine if GAIT DIFFERENCES (kinematic and kinetics) influence the rate of osteoarthritis progression as measured by articular cartilage thinning at 2 years.

Exploratory Hypothesis 2: Greater adduction moment and external rotation will be related to greater cartilage thinning (2 years - pre operative).

Exploratory Aim 3: Determine if INTRAOPERATIVE SYNOVIAL BIOPSY markers of inflammation are correlated with osteoarthritis progression.

Exploratory Aim 4: Determine if FINDINGS FROM ADVANCED MR IMAGING (T1Rho, Sodium, Diffusion) are correlated with osteoarthritis progression.

Conditions
Meniscus Tear
Being tested
Randomized Meniscectomy, Randomized Lavage, Standard of Care Meniscectomy Pre-Amend, Standard of Care Meniscectomy Post-Amend
Keywords
menisci, tibial

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Randomized MeniscectomyProcedure or surgery

    Arthroscopic meniscectomy

  • Randomized LavageProcedure or surgery

    Arthroscopic Lavage

  • Standard of Care Meniscectomy Pre-AmendProcedure or surgery

    Arthroscopic meniscectomy

  • Standard of Care Meniscectomy Post-AmendProcedure or surgery

    Arthroscopic meniscectomy

Study groups in NCT01931735
Study groupRoleWhat they receive
Randomized MeniscectomyExperimentalThis group will have a partial meniscectomy
Receives: Procedure: Randomized Meniscectomy
Randomized LavageActive comparatorThis group will have arthroscopy and lavage
Receives: Procedure: Randomized Lavage
Standard of Care Meniscectomy Pre-AmendOtherPre-Amendment: surgeons determined standard of care option, meniscectomy, best benefited the patient. Therefore, the patient was not randomized.
Receives: Procedure: Standard of Care Meniscectomy Pre-Amend
Standard of Care Meniscectomy Post-AmendOtherPost Amendment: patients received a meniscectomy as a standard of care and were observed for 24-months post-operative.
Receives: Procedure: Standard of Care Meniscectomy Post-Amend

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. WOMET Score

    Western Ontario Meniscal Evaluation Tool (WOMET) is a standardized and validated survey used to evaluate the pain and function of patients with a degenerative meniscal tear. The survey consists of 16 questions regarding physical symptoms, sports/recreation/work/lifestyle, and emotions. Each question is answered via a visual analog scale (VAS) of 0-100mm for a total score of 1600, where higher numbers are worse. The score is then transformed into a percentage, where 0 is the worst pain and functioning and 100% is no pain and fully functioning.

    Measured: one year post baseline

  2. WOMET Score

    Western Ontario Meniscal Evaluation Tool (WOMET) is a standardized and validated survey used to evaluate the pain and function of patients with a degenerative meniscal tear. The survey consists of 16 questions regarding physical symptoms, sports/recreation/work/lifestyle, and emotions. Each question is answered via a visual analog scale (VAS) of 0-100mm for a total score of 1600, where higher numbers are worse. The score is then transformed into a percentage, where 0 is the worst pain and functioning and 100% is no pain and fully functioning.

    Measured: two years post baseline

  3. Gait Knee Adduction Moment

    Knee adduction moment describes the medial/lateral load distribution of the knee measured while walking in a gait laboratory. Before normalization to account for size, the knee adduction moment is expressed in Nm. However, to account for different sized people, the knee adduction moment is transformed and expressed in percentage of body weight times height (%BW*ht). Higher knee adduction moments have been linked to more severe osteoarthritis (OA).

    Measured: Two year post baseline

  4. Average Rotation During Stance

    Degree of external tibial rotation averaged over the stance phase of gait.

    Measured: Two years post baseline

Secondary outcomes (3)
  1. KOOS Pain Score

    Knee injury and Osteoarthritis Outcome Score (KOOS) is a standardized and validated survey used to evaluate the condition of osteoarthritis of the knee. The KOOS Pain scale consists of 9 questions, with each response valued on an ordinal scale of 0-4, and with at total score of 36. Higher numbers indicate more symptoms and physical disabilities. The score is then transformed into a percentage, where 0% is the worst pain and 100% is no pain.

    Measured: two years post baseline

  2. KOOS Pain Score

    Knee injury and Osteoarthritis Outcome Score (KOOS) is a standardized and validated survey used to evaluate the condition of osteoarthritis of the knee. The KOOS Pain scale consists of 9 questions, with each response valued on an ordinal scale of 0-4, and with at total score of 36. Higher numbers indicate more symptoms and physical disabilities. The score is then transformed into a percentage, where 0% is the worst pain and 100% is no pain.

    Measured: one year post baseline

  3. TNFa

    Tumor necrosis factor-alpha (TNFa) is a pro-inflammatory cytokine that has been linked to the presence of radiographic signs of osteoarthritis (OA), cartilage volume loss over time, increased disease severity, and risk of OA progression. Elevated presence of TNFa can indicate more risk for OA. The unit of measure is pg/mL.

    Measured: Baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Aug 2013 (estimated)
  2. Study start1 Oct 2013
  3. Primary completion31 Jan 2018
  4. Study completion31 Jan 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Single group
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
27 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01931735
Sponsor's protocol ID
E0924-R
Other IDs
1I01RX000924-01A2
Status last verified
Oct 2018
First submitted
23 Aug 2013
Last updated
21 Nov 2018
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Edd SN, Giori NJ, Andriacchi TP. The role of inflammation in the initiation of osteoarthritis after meniscal damage. J Biomech. 2015 Jun 1;48(8):1420-6. doi: 10.1016/j.jbiomech.2015.02.035. Epub 2015 Feb 26.

    PubMed 25798759
  • Edd SN, Netravali NA, Favre J, Giori NJ, Andriacchi TP. Alterations in knee kinematics after partial medial meniscectomy are activity dependent. Am J Sports Med. 2015 Jun;43(6):1399-407. doi: 10.1177/0363546515577360. Epub 2015 Mar 31.

    PubMed 25828080

Questions about this trial

What is this clinical trial studying?

A study testing Randomized Meniscectomy and Randomized Lavage in people with Meniscus Tear, run by VA Office of Research and Development at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 21 Nov 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 26 Oct 2018). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

WOMET Score (time frame: one year post baseline). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01931735, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Nov 2018; AzTrials last refreshed its copy on 8 Nov 2026.

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