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Meniscus Tear clinical trials

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NCT ID: NCT06162117 Not yet recruiting - Meniscus Tear Clinical Trials

Validity and Reliability of the Two-Minute Step Test in Traumatic Meniscal Tear

Start date: February 21, 2024
Phase: N/A
Study type: Interventional

This study is designed to explore the validity and reliability of the two-minute walk test as an assessment method for functional capacity in patients diagnosed with traumatic meniscal tear. The objective is to determine the effectiveness of this test in accurately measuring the functional abilities of individuals with traumatic meniscus tears. By focusing on patients who have been diagnosed with such injuries and employing the two-minute walk test, the study aims to provide valuable insights into the suitability of this evaluation tool for assessing functional capacity in this specific patient population. The findings of this research have the potential to contribute significantly to the clinical understanding and management of traumatic meniscal tears, offering clinicians a reliable and valid method for evaluating the functional capabilities of affected individuals.

NCT ID: NCT06048341 Not yet recruiting - Meniscus Tear Clinical Trials

FNB in Meniscal Tear Under SA

Start date: September 18, 2023
Phase: N/A
Study type: Interventional

The investigators will compare the results of sono-guided femoral nerve block in arthroscopic surgery for meniscal tear under spinal anesthesia

NCT ID: NCT06045884 Not yet recruiting - Meniscus Tear Clinical Trials

FNB in Meniscal Tear Under GA

Start date: September 18, 2023
Phase: N/A
Study type: Interventional

The investigators will compare the results of sono-guided femoral nerve block in arthroscopic surgery for meniscal tear under general anesthesia

NCT ID: NCT06041763 Not yet recruiting - Meniscus Tear Clinical Trials

Bridge-Enhanced ACL Repair (BEAR) in Meniscus Repair

Start date: April 1, 2024
Phase: N/A
Study type: Interventional

The bridge-enhanced ACL repair (BEAR) implant is a collagen-based scaffold loaded with whole blood. It is designed to promote healing in the setting of intraarticular knee pathology. This study would compare clinical outcomes and synovial fluid cytokine profiles in patients who undergo isolated meniscal repair with or without the BEAR implant.

NCT ID: NCT05909865 Not yet recruiting - Meniscus Tear Clinical Trials

PRedIcting MEniscal Tears Outcomes After Physical Therapy Treatment

PRIME
Start date: May 1, 2024
Phase: N/A
Study type: Interventional

The aim of this multicenter non-controlled study is to develop a multivariable prediction model of pain/disability improvements in patients with meniscal tears, after a physical therapy treatment based on therapeutic exercise and education.

NCT ID: NCT05505747 Not yet recruiting - Meniscus Tear Clinical Trials

Enhancing Recovery Through a Combined Mechanobiologic Intervention Following Meniscus Repair

Start date: July 2025
Phase: Phase 2/Phase 3
Study type: Interventional

Arthroscopic meniscal procedures are the most commonly performed orthopaedic procedure in the U.S. affecting 15% of Americans ages 10-65 years. Meniscus injury is also known to increase the risk of posttraumatic osteoarthritis (PTOA). The current randomized clinical trial will test a novel intervention after meniscal repair that combines an oral senolytic fisetin and real-time biofeedback program to restore joint loading and subsequent return to activity.

NCT ID: NCT05491564 Not yet recruiting - Meniscus Tear Clinical Trials

SoftStitchâ„¢ for All-Inside Meniscal Repair: Comparative Analysis of Patient Reported Outcome Measures

Start date: July 1, 2023
Phase:
Study type: Observational

Acute and traumatic knee meniscus tears are a frequent occurrence. Evidence shows meniscal repair results in more favorable patient reported outcomes and articular cartilage preservation.1 This prospective, multicenter, single cohort, longitudinal study is intended to evaluate the effectiveness and safety profile of SoftStitchâ„¢ when used as standard of care for All-Inside Meniscal Repair. Electronic Patient Reported Outcome Measures (ePROM), functional assessments of the knee, Adverse Events of interest and Adverse Device Effects will be assessed.