- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04983992
Prospective Clinical Study of Excessive Lateral Pressure Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Excessive Lateral Pressure Syndrome (ELPS) is a series of clinical symptoms caused by various factors, such as patella tilt, adaptive contraction of the Lateral retinaculum and unbalanced Pressure on the medial and Lateral joint surfaces of the patellofemoral. The concept was first proposed by Ficat in 1977. Patellofemoral pain syndrome has long been lumped together as widespread pregenitual pain and Patella malalignment syndrome as Patellofemoral pain due to poor Patella alignment.Kramer et al. found that the main cause of patellofemoral pain and increased pressure on the lateral patellofemoral surface was excessive pressure on the lateral retinol. Later, this view was accepted by more scholars, and lateral patellofemoral compression syndrome was gradually regarded as an independent syndrome and more studies were conducted.
In patients with lateral patella compression syndrome, early manifestations are usually pain in the soft tissues around the patella. Fulkerson et al. in 1985 found pathological changes in the nerve fibers in the lateral retinaculum through a pathological study, which is the basis for early lesions showing only pain in the soft tissues around the patella.As the disease progresses, uneven pressure on the medial and lateral facets of the patellofemoral joint will gradually lead to damage of the medial and lateral facets of the articular cartilage, eventually leading to irreversible damage of the articular cartilage and osteoarthritis.
The surgical treatment of lateral compression syndrome is varied, and in recent years, the most commonly used surgical methods include: incision lysis, percutaneous lysis, arthroscope-assisted percutaneous lysis, arthroscopic release, etc.These traditional surgical methods all have obvious complications, such as intraarticular dislocation of patella, recurrence of lateral compression due to postoperative adhesion of the support band, patellofemoral joint instability, intraarticular hematoma, etc.Although there are many surgical treatment methods for lateral compression syndrome, there is still no recognized standard treatment. Due to the fact that its effect and evaluation criteria cannot be unified, accurate horizontal comparison cannot be made among different regions and different populations.
Made by the researchers of the lateral retinaculum extracapsular release, at the same time in the release of the lateral retinaculum complete retaining articular capsule and lateral patellofemoral ligament, this procedure can obviously improve patellofemoral joint trajectory anomalies and significantly reduce joint surface pressure, at the same time reduce the surgical trauma, try to keep the original structure, can greatly reduce the postoperative complications of patellofemoral joint.
Studied in this paper in March 2021 to March 2022 to undergraduate course to see a doctor and accept the lateral retinaculum capsule of external release the prospective study of 100 patients with follow-up, compared with preoperative and postoperative imaging data, clinical manifestations, signs, etc., to evaluate the surgical effect, at the same time of resection specimens for pathology and genetics research,To investigate the pathogenesis of lateral patella compression syndrome.
Through this study, to explore the etiology, development and outcome of the disease, is helpful for the early diagnosis and treatment of the disease, avoid the irreversible injury of the patient's knee joint, greatly improve the quality of life of patients, reduce the incidence of knee replacement, and save medical resources.At the same time, the external capsule release of the lateral retinacular joint created by the present study will have a profound impact on the surgical treatment of the lateral retinacular joint.
Study Type
Enrollment (Anticipated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Inclusion criteria:
- Age <40.
- Normal strength line of lower limbs: no valgus or varus feet (HKA <±5°)
Exclusion Criteria:
- Combined patella dislocation and medial retinacular injury.
- Have a history of knee surgery, knee injury and fracture.
- Complicated cruciate ligament injury and medial and lateral collateral ligament injury.
- Combined knee osteoarthritis.
- Complicated with rheumatism, rheumatoid arthritis and other types of arthritis
- Patellar bisection, trochlear dysplasia
- Gouty arthritis and hyperuricemia of the knee
- Complicated meniscus injury of degree III or above
- Incorporating lateral discoid meniscus
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
observation group
People suffered from excessive lateral pressure syndrome with extracapsular release of lateral retinaculum.
|
A new kind of surgery releases the lateral retinaculum from outside the knee capsular, maintaining the structure of the knee capsular.
|
control group
People suffered from excessive lateral pressure syndrome with conservative treatment
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change of lesions
Time Frame: 2years
|
The improvement of cartilage injury of patellofemoral joint and tibiofemoral joint.
Two senior surgeons read the MRI separately, recording the status of lesion area.
The lesion area was compared before and after surgery.
Using Outerbridge Classification to evaluate the severity of cartilage injury.
|
2years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain severity change
Time Frame: 2years
|
Using Visual Analog Pain Scale for pain evaluating pain severity.The score ranks from 0 to 10. 0 means "no pain", 10 means "the pain is intolerable".
The higher the score, the more pain the patient suffers.
|
2years
|
Clinical symptom change
Time Frame: 2years
|
Using Kujala score for symptom change.
|
2years
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- M2020527
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Excessive Lateral Pressure Syndrome
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Peking University Third HospitalTerminatedExcessive Lateral Pressure Syndrome
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Bai Wen-PeiUnknownMenopausal Syndrome | Lipid Depletion | Excessive Physical Exercise, Unspecified
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Peking University Third HospitalCompletedLateral Patellar Compression SyndromeChina
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Peking University Third HospitalCompletedLateral Patellar Compression SyndromeChina
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Istituto Auxologico ItalianoRecruiting
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CephalonCompletedNarcolepsy | Excessive Daytime Sleepiness | Obstructive Sleep Apnea/Hypopnea Syndrome (OSAHS)United States
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Merck Sharp & Dohme LLCTerminatedSleep Apnea, Obstructive | Hypopnea Syndrome | Excessive Daytime Sleepiness
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Tan Tock Seng HospitalCompletedPressure Ulcer | Pressure Injury | Immobility SyndromeSingapore
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Karolinska InstitutetCompleted
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Assistance Publique - Hôpitaux de ParisCompletedHealthy Subjects | Kleine-Levin SyndromeFrance
Clinical Trials on extracapsular release of lateral retinaculum
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Peking University Third HospitalTerminatedExcessive Lateral Pressure Syndrome
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Hospices Civils de LyonActive, not recruitingEpisodic Patellar DislocationFrance
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Hospital del MarCompletedAnterior Knee Pain SyndromeSpain
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Hawler Medical UniversityCompleted
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Chinese University of Hong KongCompletedHallux Valgus | Hallux Valgus and BunionHong Kong
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Jakub AntczakCentrum Neurologii Klinicznej Krakowska Akademia NeurologiiCompletedCarpal Tunnel SyndromePoland
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Peking University Third HospitalCompletedRecurrent Peroneal Tendon Dislocation
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Southern Medical University, ChinaRecruitingChiari Malformation | Basilar Invagination | Atlantoaxial DislocationChina
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Fondation Ophtalmologique Adolphe de RothschildCompletedProximal Femoral Fracture
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St Joseph University, Beirut, LebanonUnknown