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Anterior Cruciate Ligament Tear clinical trials

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NCT ID: NCT03776162 Recruiting - Clinical trials for Anterior Cruciate Ligament Tear

A Comparison of ACL Repair With BEAR Device vs. Autograft Patellar Tendon ACL Reconstruction

BEAR-MOON
Start date: August 30, 2021
Phase: N/A
Study type: Interventional

This study is designed to evaluate bridge-enhanced ACL restoration (BEAR), a new surgical technique for repairing knees injured by a tear of the anterior cruciate ligament (ACL) that promotes reattachment and healing of the ACL using a blood-enriched implant. BEAR will be compared to bone to patellar tendon to bone autograft (BPTB) reconstruction, a standard ACL surgical reconstruction technique that replaces a torn portion of the ACL with transplanted patellar tendon tissue, and thus requires additional invasive patellar tendon removal and reuse as a portion of the ACL surgery, in a two group randomized clinical trial (RCT) in which participants will have equal chance of receiving BEAR or BPTB reconstruction. The BEAR technique is FDA approved and involves surgically placing a sponge (the BEAR implant) between the torn ends of the ACL, providing an absorbable implant for the ligament ends to grow into. The investigators hypothesize that the ACL repair with BEAR technology will achieve results not appreciably worse than BPTB reconstruction, with a reduced burden of invasive surgery, when assessed over the first two post-operative years. Animal studies suggest BEAR may also ameliorate longer-term premature osteoarthritis of the knee, a common consequence of ACL reconstruction surgery. However, no human data yet support that, and this trial will conclude before such a benefit can be observed. All patients 18-55 years of age who are candidates for ACL surgery within 50 days of the ACL injury and who present to surgeons participating in the study will be offered participation in the trial. Patients will be randomized and will undergo specified rehabilitation protocols post-operatively with primary assessments of knee laxity and patient reported measures at 6 months, 1 year, and 2 years.

NCT ID: NCT02930122 Terminated - Clinical trials for Anterior Cruciate Ligament Tear

IL-1RA Treatment in Patients With Acute ACL Tear and Painful Effusions

EASI ACL
Start date: June 20, 2019
Phase: Phase 2
Study type: Interventional

Injury to the knee during sports participation often involves partial or full detachment of the anterior cruciate ligament (abbreviated as ACL). ACL tears cause pain, swelling and inflammation. While the swelling and inflammation usually goes away in time, individuals with ACL injuries may experience pain and notice knee instability (knee slipping, etc.). Often surgery can repair or replace the ACL within the joint, allowing individuals the ability to walk or run again pain free or participate in sports. Unfortunately, osteoarthritis of the knee, which also causes pain and swelling, can occur in that same knee 10-20 years later for reasons which are not well understood. In this research study, the investigator hopes to reduce the initial pre-operative pain. The reduction of pain will allow for earlier movement of the knee joint and preparation for surgery. The investigator is interested to see if the use of Kineret does decrease the risk of developing arthritis in individuals with ACL injuries by treating them within 28 days after their injury.

NCT ID: NCT02911909 Terminated - Clinical trials for Anterior Cruciate Ligament Tear

Moderated Blood Flow Restriction After Anterior Cruciate Ligament Reconstruction

Delfi
Start date: October 1, 2017
Phase: N/A
Study type: Interventional

The aim of this study is to determine if there is a difference in post operative rehabilitation after anterior cruciate ligament (ACL) reconstruction surgery while using moderated blood flow therapy vs. standard physical therapy. All patients undergoing ACL reconstruction, between the ages of 18-30, that consent to taking part in the study, and meet eligibility criteria, will be included in the study. Patients will be followed for two years to determine any differences in muscle strength, thigh circumference, knee range of motion, pain, functional and activity levels, patient satisfaction, levels of Human growth hormone HGH), Insulin-like Growth Factor (IGF), and Creatine Kinase (CK), KT2000, and Lachman physical examination.

NCT ID: NCT02787096 Completed - Clinical trials for Anterior Cruciate Ligament Tear

Dynamic Knee Laxity Measurement Coupled to MRI in Cases of Suspected Partial Anterior Cruciate Ligament Tear

LaxIRM
Start date: May 9, 2012
Phase: N/A
Study type: Interventional

Anterior cruciate ligament (ACL) tear is frequent, but the diagnosis of partial tears is difficult. Standard MRI may be used but is of limited diagnostic value. The present study aimed to evaluate the diagnostic interest of dynamic knee laxity measurement coupled to MRI for the diagnosis of ACL tear.

NCT ID: NCT02760589 Completed - Clinical trials for Anterior Cruciate Ligament Tear

Magnetic Resonance Imaging and Functional Performance Outcome After ACL Repair With Internal Brace Technique

Start date: November 2015
Phase:
Study type: Observational

The purpose of the study is a clinical evaluation with special regard to magnetic resonance imaging and functional performance at least one year after injury / surgery in all three groups (subjects who underwent InternalBrace surgery, subjects who underwent surgery with a semitendinosus graft and subjects who were treated conservatively).

NCT ID: NCT02664545 Active, not recruiting - Clinical trials for Anterior Cruciate Ligament Tear

Bridge-Enhanced ACL Repair vs ACL Reconstruction

Start date: April 2016
Phase: N/A
Study type: Interventional

The goal of this trial is to compare the efficacy of the Bridge-Enhanced Anterior Cruciate Ligament Repair (BEAR™) technique with the current method of treatment for anterior cruciate ligament (ACL) injuries, ACL reconstruction.

NCT ID: NCT02292004 Active, not recruiting - Clinical trials for Anterior Cruciate Ligament Injury

Bridge-Enhanced ACL Repair-Safety Study (BEAR Trial)

BEAR
Start date: January 2015
Phase: N/A
Study type: Interventional

This study will assess the safety and early efficacy of a newly developed device, bridge-enhanced scaffold (MIACH™,) used to repair a torn anterior cruciate ligament (ACL.) Ten participants will undergo surgery with the new device (Experimental Group) and 10 will undergo a standard ACL reconstruction surgery (Control Group.)

NCT ID: NCT01850758 Completed - Clinical trials for Anterior Cruciate Ligament Tear

Regenexx™ SD Versus Exercise Therapy for ACL Tears

Start date: May 2013
Phase: N/A
Study type: Interventional

The primary objective of this study is to compare the improvement in subject-reported clinical outcomes for Regenexx SD vs. Exercise Therapy treatment of partial and complete, non-retracted knee ACL ligament tears, from baseline to 3 months, with continued evaluation of efficacy and durability up to 24 months. Secondary objectives include evaluation of MRI evidence of tendon repair; incidence of post-operative complications, adverse events, re-injections, and surgical intervention; change in pain score and use of pain medications.

NCT ID: NCT01580722 Completed - Clinical trials for Anterior Cruciate Ligament Tear

Comparison of Early Versus Delay Reconstruction in Anterior Cruciate Ligament Tearing

Start date: March 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine which surgical method is better for anterior cruciate ligament teas in outcomes.

NCT ID: NCT01447277 Completed - Clinical trials for Anterior Cruciate Ligament Tear

Prospective Femoral Versus Femoral and Sciatic Nerve Block for Anterior Cruciate Ligament (ACL) Reconstruction

Start date: October 2011
Phase: N/A
Study type: Interventional

The investigators propose that a preoperative femoral and sciatic blocks vs a femoral block only, prior to ambulatory anterior cruciate ligament (ACL) reconstruction will lead to a decrease in opiate consumption, pain scores, and post-anesthesia care unit (PACU) length of stay. The investigators are prospectively randomizing patients to either a femoral or a fem/sciatic block and monitor outcomes.