← Back to Clinical Trials
Recruiting NCT07501013

NCT07501013 Clinical Outcomes of Arthroscopic Surgeries for Shoulder and Knee Sports Injuries

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07501013
Status Recruiting
Phase
Sponsor Second Affiliated Hospital, School of Medicine, Zhejiang University
Condition Athletic Injuries (C26.857.500.124)
Study Type OBSERVATIONAL
Enrollment 500 participants
Start Date 2026-04-07
Primary Completion 2046-04-07

Trial Parameters

Condition Athletic Injuries (C26.857.500.124)
Sponsor Second Affiliated Hospital, School of Medicine, Zhejiang University
Study Type OBSERVATIONAL
Phase N/A
Enrollment 500
Sex ALL
Min Age 8 Years
Max Age 80 Years
Start Date 2026-04-07
Completion 2046-04-07
Interventions
Standard of Care Shoulder ArthroscopyStandard of Care Knee Arthroscopy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

Brief Summary

This observational study aims to evaluate the long-term recovery and clinical outcomes of patients undergoing minimally invasive (arthroscopic) surgeries for sports-related shoulder and knee injuries. Sports injuries, such as ligament tears, meniscus damage, and rotator cuff tears, are common and can significantly impact a person's daily life and ability to return to sports. While surgery is an effective treatment, the recovery process and final outcomes can vary greatly from person to person. Researchers will follow patients who are already scheduled for routine shoulder or knee surgery at the study center. By collecting detailed information about the patient's initial injury, the specific surgical techniques used by the doctor, and the patient's recovery progress over two years, the study hopes to identify which factors lead to the best healing and functional outcomes. Participants will be asked to complete standard questionnaires about their joint function and pain levels before their surgery, and again at 6 months, 1 year, and 2 years after surgery. The study is strictly observational; it will not change the standard medical care, surgical plan, or rehabilitation routine the patients receive.

Eligibility Criteria

Inclusion Criteria: * Age \>= 8 years. * No gender restrictions. * Definitive diagnosis of shoulder or knee sports injuries or related joint conditions. * Scheduled to undergo elective, standard-of-care surgery at the study center (procedures include but are not limited to: arthroscopic meniscus repair/meniscectomy, cartilage repair, cruciate ligament reconstruction, high tibial osteotomy \[HTO\], unicompartmental knee arthroplasty \[UKA\], arthroscopic rotator cuff repair, shoulder stabilization, and shoulder arthroplasty). * Clear consciousness, with the ability to read, understand, and communicate. * Willing and able to comply with postoperative follow-up requirements. * Voluntarily signed the written informed consent form. Exclusion Criteria: * Patients requiring emergency surgery due to acute, severe trauma (e.g., open fractures, polytrauma). * Coexisting severe neurological or psychiatric diseases, or cognitive impairment that prevents understanding of the informed consent or coo

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology