Meniscal Tear

5

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

Condition / disease
Location
Status: Not yet recruiting

Effect of Preoperative Kinesiophobia on Clinical Outcomes Following Arthroscopic Meniscus Surgery

Meniscal tears are among the most common knee injuries and frequently require arthroscopic surgical treatment when conservative management fails or mechanical symptoms persist. Although surgical techniques have improved clinical outcomes, postoperative recovery is influenced not only by structural pathology but also by psychological factors. Kinesiophobia, defined as an excessive and debilitating fear of movement due to pain or the expectation of reinjury, may negatively affect rehabilitation adherence, functional recovery, and pain perception. This prospective observational study aims to investigate the effect of preoperative kinesiophobia on postoperative clinical outcomes in patients undergoing arthroscopic surgery for meniscal tears. Adult patients diagnosed with a meniscal tear by clinical examination and magnetic resonance imaging and scheduled for arthroscopic surgery will be enrolled. Preoperative demographic and clinical characteristics, pain intensity, functional status, and kinesiophobia levels will be assessed using validated outcome measures. Postoperative evaluations will be performed three months after surgery to determine changes in pain and functional outcomes. The relationship between preoperative kinesiophobia and postoperative clinical success will be analyzed. The findings of this study may help identify patients at risk for suboptimal recovery and support the development of individualized rehabilitation strategies.

Participants needed: 50
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Medipol UniversityUpdated: Jun 17, 2026
Eligibility criteria

Not listed

Status: Not yet recruiting

Semitendinosus Autograft vs Meniscal Allograft in Post-Meniscectomy Syndrome

This multicenter, stratified, partially randomized clinical trial aims to compare autologous semitendinosus tendon graft and meniscal allograft transplantation (MAT) in young adults with post-meniscectomy syndrome. The meniscus plays a critical role in load distribution, shock absorption, and joint stability. After meniscectomy, insufficient meniscal tissue often leads to persistent pain, swelling, and functional decline, increasing the risk of early osteoarthritis. Two reconstructive strategies are clinically available: MAT provides immediate biomechanical function but requires donor matching and carries higher costs, while autologous tendon graft offers stable supply and no immunologic risk but lacks long-term clinical validation. In this study, 40 patients aged 18-45 years will be enrolled. Participants will be allocated into four groups (randomized MAT, randomized autograft, patient-preference MAT, patient-preference autograft). All procedures will use a two-tunnel fixation technique with additional internal brace support. The primary endpoint is the improvement in KOOS (Knee Injury and Osteoarthritis Outcome Score) at 24 months postoperatively. Secondary endpoints include MRI-based assessment of graft morphology and extrusion, reoperation rate, complications, patient satisfaction, and return-to-sport time. This trial will provide critical evidence regarding the comparative effectiveness and feasibility of tendon autograft versus meniscal allograft in real-world clinical settings, potentially informing surgical decision-making and future treatment guidelines for post-meniscectomy syndrome.

Participants needed: 40
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Chang Gung Memorial HospitalUpdated: Oct 2, 2025Locations: 1
Eligibility criteria

Adults aged 18 to 45 years

Status: Recruiting

This is a Study to Verify if Marrow Venting Procedure Can Improve Meniscal Suture Healing

Meniscal suture represents the current surgical practice, and marrow venting is a low risk procedure. Bone venting may be able to improve the outcome of meniscal repair, allowing the patient a better recovery.

Participants needed: 80
Trial details
Age: 16-50Biological sex: AllType: InterventionalSponsor: Christian CandrianUpdated: Aug 6, 2025Locations: 2
Eligibility criteria

Arthroscopic confirmed suturable meniscal tears, [+4]

Bilateral meniscal tears requiring treatment, [+9]

Status: Recruiting

Partial Meniscal Replacement with Spongioflex®

The purpose of this investigator-initiated trial is to evaluate whether the novel graft can prevent/reduce the disadvantages of the previously used replacement materials and shows better results than the group of patients, which were not operated. Since there is currently no alternative made of biological material to this product, this investigator-initiated trial is of great medical and economic importance. The otherwise following arthrosis or knee prosthesis implantation (TKA ) could be prevented or at least postponed. Initial clinical results are promising. An important and sensitive parameter for assessing the postoperative function of the meniscus is the MRI image. Genovese et al. 2007 were able to show in a categorization/classification which magnetic resonance image can be expected in the case of successful incorporation. Several studies have shown that the known clinical knee scores (Lysholm, IKDC, KOOS, VAS pain) improve significantly after successful ingrowth of the meniscus implant.

Participants needed: 40
Trial details
Phase: Phase 4Age: 18-60Biological sex: AllType: InterventionalSponsor: Maria-Josef-Hospital GrevenUpdated: Jan 15, 2025Locations: 1
Eligibility criteria

Partial loss of portions of the [+5]

The presence of anterior cruciate ligament insufficiency which is not resolved b... [+15]

Status: Not yet recruiting

Nanoscope Cost Analysis Study

The study is a pilot study designed to generate preliminary data regarding the cost of partial meniscectomy using NanoScope versus conventional arthroscopy in a traditional operating room (OR) setting

Participants needed: 10
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Arthrex, Inc.Updated: Sep 19, 2024Locations: 1
Eligibility criteria

Subject requires simple partial posterior or mid-body meniscectomy. [+5]

Subject requires complex repair or anterior meniscectomy. [+15]