ACL Surgery

6

Review clinical trials related to ACL Surgery. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

The Effect of Isokinetic Vs Plyometric Training in Post-ACLR Surgery

The primary goal of this RCT is to evaluate the effects of isokinetic training compared to plyometric training after 4weeks of intervention in patients aged 18-40 years who have undergone ACLR surgery. The primary question to answer is which of the two interventions (isokinetic or plyometrics) has superior effect in the improvement of muscular strength, functional performance and patient-reported outcomes in ACLR patients. Participants will be divided into two groups. both groups received standard rehabilitation for 4 weeks, followed by adding: Group 1: receives isokinetic training, Group 2: receives plyometric training.

Participants needed: 40
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Oct 7, 2026Locations: 1
Eligibility criteria

Age 18-40 years [+4]

Revision ACL reconstruction [+5]

Status: Recruiting

The Effect of Plyometric Training in Post-ACLR Surgery

The primary goal of this RCT is to evaluate the effect of adding plyometric training after 12 weeks of standard intervention in patients aged 18-40 years who have undergone ACLR surgery. The primary question to answer is does adding plyometrics training to the standard rehabilitation program has superior effect in the improvement of muscular strength, dynamic balance and functional performance in ACLR patients. Participants will be divided into two groups. Group 1 receives standard program for 18 weeks, and Group 2 receives the same standard program for 18 months, but adding the plyometrics training at week 12.

Participants needed: 40
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Oct 7, 2026Locations: 1
Eligibility criteria

Age 18-40 years [+4]

Revision ACL reconstruction [+5]

Status: Not yet recruiting

Human Tendon Tissue Collection

The goal of this study is to improve understanding of tendon health and disease by using surplus tendon tissue that is routinely removed during planned orthopaedic surgeries in adults. The main questions it aims to answer are: \- What can tendon tissue and tendon cells tell us about how healthy and diseased tendons function? Participants will not undergo any extra procedures. Instead, researchers will use only tissue that is already being removed as part of normal surgical care and would otherwise be discarded. Participants will: * Be asked for permission (consent) before their surgery to donate any surplus tendon tissue. * Have a small piece of tendon tissue (normally waste material) collected during their planned operation. * Allow the research team to access some non-identifiable medical information (such as age, reason for surgery, and relevant medical history) to help interpret research findings. What the researchers will do with the donated tissue: * Isolate different types of human tendon cells. * Build advanced laboratory cellular models to study how tendon diseases develop. * Analyse whole tendon tissue sections to understand cell types, tissue organisation, and disease-related changes. This study does not involve testing treatments, and it does not change any aspect of a participant's clinical care. Although there is no direct benefit to participants, the donated tissue may help researchers develop better ways to study tendon injuries and improve future treatment options for tendon disease.

Participants needed: 400
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Queen Mary University of LondonUpdated: Oct 7, 2026Locations: 2
Eligibility criteria

18 years or older [+2]

Under the age of 18 [+2]

Status: Recruiting

Muscle Function Following Anterior Cruciate Ligament Reconstruction: Impaired Power Output in Physically Active Individuals

The goal of this clinical trial is to to determine the extent of the association between objective changes in the muscle function of the knee extensors (strength and power) and the function reported by the patient following ACL reconstruction surgery. The main questions it aims to answer is: \- Pre- and post-operative (6 months) changes in maximum knee extensor strength following ACL reconstruction, correlated with the IKDC-SKF score.

Participants needed: 110
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Metropole SavoieUpdated: Aug 14, 2026Locations: 1
Eligibility criteria

Patients requiring isolated or complex ACL reconstruction (combined with a menis... [+5]

Patient with comprehension difficulties [+2]

Status: Recruiting

Efficacy of Methylprednisolone for Pain Control After ACL Repair

Opioids are commonly used after orthopedic surgery for pain control but have been shown to increase complications, surgeries, readmissions, and risk for opioid use disorder. The purpose of this study is to investigate the impact of adding a methylprednisolone taper to the pain regimen after ACL repair surgery to determine if this results in decreased postoperative pain and opioid use without increasing complications.

Participants needed: 90
Trial details
Phase: Phase 4Age: 13-50Biological sex: AllType: InterventionalSponsor: St. Louis UniversityUpdated: Oct 24, 2025Locations: 1
Eligibility criteria

Patient undergoing ACL repair or ACL reconstruction with tendon autograft [+2]

Concurrent and significant injury to other bones or organs (Injury Severity Scor... [+8]

Status: Not yet recruiting

KEA vs Towel for Early Quad Activation Post Anterior Cruciate Ligament Reconstruction

The goal of this clinical trial is to learn if a novel Knee Extensors Activation (KEA) device can improve quadriceps muscle activation in adults after anterior cruciate ligament (ACL) reconstruction surgery. The study focuses on adults aged 18-45 years undergoing primary unilateral ACL reconstruction, a population commonly affected by this injury. The main questions it aims to answer are: Does using the KEA device lead to greater quadriceps muscle activation (measured via EMG) by postoperative Day 5 compared to standard care using a rolled towel? Does the KEA device improve early knee function, reduce pain, and decrease fear of movement compared to the towel method? Researchers will compare participants using the KEA device versus a control group using the conventional rolled towel during early postoperative rehabilitation to see if the KEA device provides better outcomes. Participants will: Begin quadriceps strengthening exercises on the first day after ACL surgery. Be randomly assigned to use either the KEA device or a rolled towel for isometric quadriceps exercises. Perform 3 sets of 10 repetitions of knee extension exercises, twice daily for 5 consecutive days. Undergo assessment of quadriceps EMG activation and complete questionnaires (KOOS, IKDC, TSK, and VAS) on Day 5.

Participants needed: 40
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Jouf UniversityUpdated: Jun 27, 2025
Eligibility criteria

Adults aged 18 to 45 years [+4]

Bilateral knee surgeries (e.g., simultaneous ACL reconstruction on both knees) [+5]