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Highlights a New Clinical Sign Which Point Out a Meniscus Posterior Luxation Because of a MCA-type DLMNCT04741269

Asymmetric Lack of Knee Flexion as a Symptom of DLM in Children

An observational study of Highlights a New Clinical Sign Which Point Out a Meniscus Posterior Luxation Because of a MCA-type DLM, run by Hospices Civils de Lyon at 1 site in France.

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

Highlighted during the clinical examination of a knee flexion asymmetry, and related to the intraoperative meniscal observations on DLM. Search for a link between asymmetric bending defect and posterior shift in MCA-type DLM. Analysis of all patients with symptomatic DLM. Read more about this study

Who is it for?
Ages 0 to 18 years
What is being tested?
Find a link between lack of knee flexion and meniscal posterior luxation fixed
How many people
98 participants
Where
1 siteFrance
Study dates
1 Sep 2020to 31 Dec 2020
Phase
Observational
Are there results?
None posted in the registry

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 0 to 18 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Study population: Children with a discoid lateral meniscus symptomatic and surgical care.

Who may be able to join

  • < 18 yo
  • Symptomatic discoid lateral meniscus

Who cannot join

  • Osteochondritis dissecans (OCD)
  • Asymptomatic and partial DLM observed during arthroscopic exploration for other reasons
  • Revision knee surgery

Trial locations and contacts

1 site in 1 country.

France1 site
  • Paediatric orthopaedic - Femme Mère Enfant Hospital (HFME)

    Lyon, 69005

Other trials in France

About this study

Highlighted during the clinical examination of a knee flexion asymmetry, and related to the intraoperative meniscal observations on DLM.

Search for a link between asymmetric bending defect and posterior shift in MCA-type DLM.

Analysis of all patients with symptomatic DLM.

Being tested
Find a link between lack of knee flexion and meniscal posterior luxation fixed
Keywords
discoid lateral meniscus, children, instability, arthroscopy, repair, lack of flexion, flexion block knee

What participants receive

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

  • Find a link between lack of knee flexion and meniscal posterior luxation fixedDiagnostic test

    Measure the full flexion angle of the knee using a goniometer. Measure the heel-buttom distance. All measurements are carried out in bilateral and comparative ways.

    Search for the meniscal position on MRI and intraoperatively: no shift, anterior, medial, posterior shift.

Study groups in NCT04741269
Study groupRoleWhat they receive
Lack of knee flexionDuring preoperative clinical exam, highlight of a lack of knee flexion. The lack of knee flexion consists in an asymmetric heel-bottom distance or an asymmetric goniometric measure of knee flexion. All others characteristics are also analyzed like in group 2, as : rest of knee motion, MRI meniscus shift, arthroscopic shift
Receives: Diagnostic Test: Find a link between lack of knee flexion and meniscal posterior luxation fixed
Full knee flexionDuring preoperative clinical exam, highlight of a lack of knee flexion. The lack of knee flexion consists in an asymmetric heel-bottom distance or an asymmetric goniometric measure of knee flexion. Patients in group 2 don't have any asymmetric full knee flexion. All others characteristics are also analyzed like in group 2, as : rest of knee motion, MRI meniscus shift, arthroscopic shift

What is being measured

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

  1. Meniscal posterior shift per-operative

    Visualization of a dislocated posterior meniscus during arthroscopy, before any reduction or meniscoplasty procedure

    Measured: During surgery for MCA-type DLM

Timeline

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

  1. First posted5 Feb 2021
  2. Study start1 Sep 2020
  3. Primary completion1 Nov 2020
  4. Study completion31 Dec 2020

Resources

More details

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

Study design
Study type
Observational
Observational model
Other
Time perspective
Retrospective
Enrolment
98 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04741269
Sponsor's protocol ID
69HCL20_1241
Status last verified
Dec 2025
First submitted
2 Feb 2021
Last updated
19 Dec 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Highlights a New Clinical Sign Which Point Out a Meniscus Posterior Luxation Because of a MCA-type DLM, run by Hospices Civils de Lyon at 1 site in France.

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 2 inclusion and 3 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 19 Dec 2025. 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 France. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Meniscal posterior shift per-operative (time frame: During surgery for MCA-type DLM). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 19 Dec 2025.

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