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Meniscus Tear clinical trials

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NCT ID: NCT06391047 Completed - Clinical trials for Osteoarthritis, Knee

Impact of Mulligan Squeeze Technique on Meniscal Derangement in Knee Osteoarthritis Patients

Start date: February 2, 2024
Phase: N/A
Study type: Interventional

The objective of this study is to find out the effects of Mulligan's Squeeze technique added as a complementary treatment to the conventional physiotherapy for the management of meniscal derangement in knee osteoarthritis patients.

NCT ID: NCT06227078 Completed - Knee Osteoarthritis Clinical Trials

Effects of Kinesiotaping and Physiotherapy in Grade 2 Osteoarthritis Following Degenerative Meniscal Tears

Start date: September 1, 2021
Phase: N/A
Study type: Interventional

Degenerative meniscal tears are a common cause of osteoarthritis commonly diagnosed in football players and are considered a major risk factor for the development of knee osteoarthritis. This study aimed to investigate the Clinical and functional effects of kinesiotaping and physiotherapy in grade 2 osteoarthritis following degenerative meniscal tears in football players.

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: NCT06041321 Recruiting - Meniscus Tear Clinical Trials

Novel Bioactive Sleeve on Pain and PROMs

Start date: December 6, 2023
Phase: N/A
Study type: Interventional

A novel bioactive sleeve will be compared to a placebo sleeve with a similar look and feel to assess pain outcomes, patient reported outcome measures, and effectiveness of healing based on range of motion.

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: NCT05882591 Recruiting - Meniscus Tear Clinical Trials

Posteromedial Tibiofemoral Incongruence (PMTFI) Treatment

Start date: October 9, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to assess outcomes of Posteromedial Tibiofemoral Incongruence (PMTFI) Treatment

NCT ID: NCT05875480 Completed - Rehabilitation Clinical Trials

The Effectiveness of Telerehabilitation After Arthroscopic Meniscus Repair

Start date: September 23, 2021
Phase: N/A
Study type: Interventional

This study was performed on 42 patients, who underwent arthroscopic meniscus repair surgery in the Orthopedics and Traumatology Department of Acıbadem Maslak Hospital. 42 patients randomly assigned to 14 synchronized telerehabilitation, 14 asynchronous telerehabilitation, 14 conventional physiotherapy groups and included in the study. The evaluation form created for the provision of demographic information are used. Primary outcome measures are muscle strength, range of motion (ROM) and pain intensity. Secondary outcome measures are general health profile and functional status assessment of the knee joint . Evaluation methods: All evaluations were performed in the preoperative period, 10. day, 6. week and 6. month postoperatively. ROM and pain measurements repeated every week during the 6-week rehabilitation process. Pain, general health profile and functional status assessment of the knee joint were assessed via a telerehabilitation application, Albert Health Assistant. Postoperative first day, the 14-day exercise program was taught to all patients practically and was given as a brochure. Patients in the synchronized telerehabilitation group started physiotherapy postoperative 14. day, met with the physiotherapist in real time via the Albert Health Assistant application and they were treated 2 days a week until 6. week. In the remaining days, they asked to follow the exercise videos uploaded to the Albert system, it was checked whether they are doing daily exercises, and a daily reminder message was sent via the system. The exercise program for the asynchronous telerehabilitation group was uploaded to the Albert Health Assistant as a video from the 14th day in the form of 2-week programs. It was checked over the system whether the patients apply these videos on a daily basis, and a message reminding the daily routine exercise program was sent through the system. Patients in the supervised physiotherapy group started to take supervized rehabilitation after 10-14 days postoperatively, 2 times a week until 6th week postoperatively in Maslak Acıbadem Hospital Orthopedics and Traumatology Department. ROM, Pain, functional and general health evaluations of the patients in this group were performed on the online platform. In addition, daily routine exercises will be followed over the Albert system on the days they do not come for treatment.