Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06233305
Other study ID # 202414
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 3, 2024
Est. completion date March 27, 2025

Study information

Verified date March 2024
Source Taipei Hospital, Ministry of Health and Welfare
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Background: The anterior cruciate ligament(ACL) , one of the major ligaments in the knee joint which connects the posterior aspect of the lateral femoral condyle to the anterior intercondylar area of the tibia. It plays a crucial role in maintaining knee joint stability, preventing excessive rotation of the tibia, and controlling the angles of knee valgus and varus. Additionally, the ACL contains mechanoreceptors that contribute to proprioception input. Acute ACL injuries are characterized by joint effusion, instability, and reduced range of motion. In the chronic phase, instability and pain may occur during rotational and cutting movements. Currently, regenerative injection therapies such as high-concentration platelet-rich plasma (PRP)and bone marrow concentrate (BMC) are being explored for ACL repair. Studies have found that postoperative administration of high-concentration PRP significantly reduces pain and improves knee joint function for a duration of 3 to 6 months, but these effects are not sustained beyond 12 months. In addition, some research indicates that high-concentration PRP does not enhance graft healing or improve knee joint stability. Method: This is a single-institution, single-blind, observational study conducted by the rehabilitation department of a public hospital. The study aims to recruit 40 participants with anterior cruciate ligament (ACL) or posterior cruciate ligament (PCL) injuries. The treatment intervention is collaboratively determined by the physician and the participant during the clinic visit. Subsequently, a therapist, unaware of the treatment details, conducts baseline assessments, including basic information collection, balance testing, gait analysis, timed up and go test, muscle strength evaluation, and subjective knee assessment questionnaire. Additionally, a physician, blinded to the treatment content, employs ultrasound to assess ligament elasticity. Follow-up assessments are conducted for the same parameters two months later.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date March 27, 2025
Est. primary completion date December 27, 2024
Accepts healthy volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: 1. Age between 18 to 80 years old. 2. Magnetic Resonance Imaging (MRI) shows partial tearing of the anterior cruciate ligament (ACL) or posterior cruciate ligament (PCL), possibly combined with injuries to the medial collateral ligament (MCL) or meniscus. 3. No surgical treatment has been undergone. Exclusion Criteria: 1. Had knee joint diseases or undergone knee joint surgery before the injury. 2. Surgical intervention is required for severe damage to knee joint ligaments, meniscus, or articular tissues, such as complete rupture of lateral ligaments or full-thickness cartilage injuries. 3. Suffers from diseases affecting physical activity function, such as stroke or nerve damage.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Taipei Hospital, Ministry of Health and Welfare New Taipei City

Sponsors (1)

Lead Sponsor Collaborator
Taipei Hospital, Ministry of Health and Welfare

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Balance Sensing Test Subjects were instructed to wear knee protectors(KNEESUP Care ) equipped with 3D gyroscopes which made from Conzion and subjects were asked to perform three trials of open-eye single-leg standing and three trials of closed-eye single-leg standing. The dynamic sensing system software recorded the time spent in single-leg standing and analyzed parameters such as balance area, anterior-posterior and medial-lateral displacement of the knee joint, and differences between the two feet. Pre-treatment assessment, approximately one month later perform a mid-term assessment, and two months later, conduct a post-treatment assessment.
Primary Gait Analysis Subjects were instructed to wear knee protectors(KNEESUP Care ) equipped with 3D gyroscopes which made from Conzion. Gait analysis involves having the subjects walk back and forth for six meters while wearing the device, with the software analyzing differences in the gait of both feet. Pre-treatment assessment, approximately one month later perform a mid-term assessment, and two months later, conduct a post-treatment assessment.
Primary Time up and go test Subjects were instructed to wear knee protectors(KNEESUP Care ) equipped with 3D gyroscopes which made from Conzion. The patient stand up from the chair, walking three meters forward, turn around, and return to the chair to sit down.The KNEESUP will calculate the total time needed Pre-treatment assessment, approximately one month later perform a mid-term assessment, and two months later, conduct a post-treatment assessment.
Primary Muscle Strength Test Quantify muscle strength of knee extensors and knee flexors using a hand-held dynamometer(ISOFROCE GT-300) which made from OG WELLNESS Pre-treatment assessment, approximately one month later perform a mid-term assessment, and two months later, conduct a post-treatment assessment.
Primary International Knee Documentation Committee A total of 18 items were assessed, covering aspects such as symptoms, physical activity, and functionality. Each item was scored on a sequential scale, with higher scores indicating lower symptoms and higher functionality. The sum of all scores was calculated and then converted into a scale ranging from 0 to 100. Pre-treatment assessment, approximately one month later perform a mid-term assessment, and two months later, conduct a post-treatment assessment.
Primary Ligament elasticity Utilizing shear wave elastography, elastic images are generated by inducing shear waves within the tissue using acoustic pressure waves. The propagation speed of these waves is directly proportional to the square root of the tissue's elastic modulus. The elasticity coefficient of the anterior cruciate ligament is measured in patients at various degrees of knee flexion. Pre-treatment assessment, approximately one month later perform a mid-term assessment, and two months later, conduct a post-treatment assessment.
See also
  Status Clinical Trial Phase
Completed NCT05109871 - Reliability and Validity of Inline Dynamometry Study for Measuring Knee Extensor Torque N/A
Recruiting NCT04088227 - Effects of Platelet Rich Plasma Injections on Biomarkers After Anterior Cruciate Ligament Tears Phase 2
Completed NCT04956393 - The SOAR (Stop OsteoARthritis) Program Proof-of-Concept Study N/A
Recruiting NCT05574946 - Comparison of Two ACL Reconstruction Techniques: All-inside Versus Complete Tibial Tunnel Technique N/A
Completed NCT01447277 - Prospective Femoral Versus Femoral and Sciatic Nerve Block for Anterior Cruciate Ligament (ACL) Reconstruction N/A
Terminated NCT02911909 - Moderated Blood Flow Restriction After Anterior Cruciate Ligament Reconstruction N/A
Completed NCT02760589 - Magnetic Resonance Imaging and Functional Performance Outcome After ACL Repair With Internal Brace Technique
Completed NCT02787096 - Dynamic Knee Laxity Measurement Coupled to MRI in Cases of Suspected Partial Anterior Cruciate Ligament Tear N/A
Completed NCT04635579 - Personalized Blood Flow Restriction for Anterior Cruciate Ligament Rehabilitation N/A
Completed NCT01850758 - Regenexx™ SD Versus Exercise Therapy for ACL Tears N/A
Recruiting NCT05204836 - Altering Bone Microarchitecture and Mechanics by Off-label Pharmaceutical Intervention Following an Acute Knee Injury Phase 1
Recruiting NCT04592471 - Assessment of the Safety and Performance of Knee Ligament Supports in the Context of a Return to Sport After Sprain
Completed NCT01580722 - Comparison of Early Versus Delay Reconstruction in Anterior Cruciate Ligament Tearing Phase 2
Recruiting NCT05174611 - Vitamin D to Improve Quadricep Muscle Strength Phase 2
Recruiting NCT05501210 - Vibration on Patellofemoral Joint Pain After ACLR N/A
Recruiting NCT05682820 - Analysis of Radiological Features of Lateral Femoral Impaction Fracture / Lateral Femoral Notch Sign
Terminated NCT02930122 - IL-1RA Treatment in Patients With Acute ACL Tear and Painful Effusions Phase 2
Recruiting NCT05306054 - Physical Activity, Knee Joint Loading and Joint Health
Completed NCT04374968 - Use of Blood Flow Restriction Therapy Following ACL Tear N/A
Recruiting NCT04998656 - Werewolf Flow 50 During ACL Reconstruction N/A