Anterior Cruciate Ligament (ACL) Reconstruction

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Review clinical trials related to Anterior Cruciate Ligament (ACL) Reconstruction. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Comparison of Bone-patellar Tendon-bone and Patellar Tendon-bone Grafts in ACL Reconstruction

The purpose of this randomized study is to compare donor site morbidity and clinical and functional outcomes of both surgery techniques (bone-patellar tendon-bone (BPTB) graft versus bone-patellar tendon without patellar bone plug (PT) graft) for anterior cruciate ligament reconstruction (ACLR) in athletes. The main questions it aims to answer are: * Does PT graft reduce donor site morbidity compared to the standard BPTB graft? * Does PT technique provide clinical and functional results comparable to the BPTB technique? Researchers will compare the incidence of complications and clinical and functional outcomes between the BPTB and PT grafts groups. Patients will: * Undergo ACLR surgical intervention using one of the two assigned techniques (BPTB or PT) * Follow a two-year assessment program, including visits at three, eight, 12 and 24 months after surgery.

Participants needed: 110
Trial details
Age: 12-40Biological sex: AllType: InterventionalSponsor: Universidad de GranadaUpdated: Mar 23, 2026Locations: 1
Eligibility criteria

Time for injury to surgery of less than six months. [+4]

Previous surgery or history of ligamentous knee injuries. [+3]

Status: Recruiting

Subdermal Implant-bioabsorbable Oxandrolone Pellet For Rehabilitation Following Anterior Cruciate Ligament (ACL) Surgical Reconstruction

Rehabilitation of knee stability and function after anterior cruciate ligament (ACL) reconstruction is slow and costly. The use of anabolic steroids, such as oxandrolone, may aid in the recovery of muscle mass and strength, as well as functional capacity. Oxandrolone, derived from dihydrotestosterone, has high anabolic activity and low androgenic activity (a 13:1 ratio), making it more effective in promoting weight gain with fewer side effects compared to other steroids. Registered by the FDA and previously by ANVISA (National Health Surveillance Agency (Brazil), it is indicated for cases of post-trauma or post-surgery weight loss. The subdermal use of oxandrolone implants is proposed to release the drug directly into the bloodstream, improving efficacy and reducing issues related to oral administration. This study evaluates the safety and tolerability of the absorbable subdermal oxandrolone implant for 24 weeks versus placebo implant in both men and women as an adjuvant treatment during rehabilitation following anterior cruciate ligament (ACL) surgical reconstruction. The serum and pharmacokinetic profile of the oxandrolone implant will be monitored.

Participants needed: 96
Trial details
Phase: Phase 2Age: 18-60Biological sex: AllType: InterventionalSponsor: Science Valley Research InstituteUpdated: Feb 24, 2026Locations: 6
Eligibility criteria

Ability to confirm voluntary participation and approve the Informed Consent Form... [+15]

Confirmed or suspected pregnancy; [+37]

Status: Not yet recruiting

Comparison of Video Based Phone App vs. Supervised Preoperative Exercise for ACL Reconstruction

The goal of this clinical trial is to learn if using a phone app for exercises is as effective as working with a physical therapist before anterior cruciate ligament knee surgery. It will also check if exercising before surgery helps patients recover better compared to those who do not follow a specific exercise plan. The main questions it aims to answer are: * Does the phone app help patients improve their knee strength and movement as well as seeing a physical therapist? * Do patients who exercise before surgery have a better recovery after surgery than those who do not? Researchers will compare the phone app group to a physical therapist group and a group with no specific exercise plan to see which method works best. Participants will: * Follow an exercise plan for 4 weeks before their surgery (either using the app, with a therapist, or no specific plan). * Visit the clinic for check-ups before starting the exercises, right before the surgery, and 6 months after the surgery. * Complete simple tests and surveys to measure their knee health.

Participants needed: 66
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Dr. Lutfi Kirdar Kartal Training and Research HospitalUpdated: Jan 7, 2026Locations: 1
Eligibility criteria

Patients with a diagnosed unilateral Anterior Cruciate Ligament (ACL) rupture [+3]

Patients with multiple ligament injuries (e.g., combined ACL and PCL/MCL injury)... [+4]

Status: Recruiting

M-ARS ACL Post-marketing Surveillance Study

The goal of this study is to evaluate the performance of Medacta Anatomic Ribbon Surgery (M-ARS) in patients requiring anterior cruciate ligament (ACL) reconstruction. The main goal is to evaluate the survival rate of M-ARS ACL at 6 months post-operatively. The secondary goals are to assess the survival rate, clinical and functional outcomes, the quality of life, and the rate of complications at 1 month, 1 year and 2 years post-operatively.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Medacta International SAUpdated: Mar 13, 2023Locations: 3
Eligibility criteria

Patients older than 18 years [+1]

Patients with malignant diseases (at the time of surgery) [+3]