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Clinical Trial NCT07501013 (SK-COHORT) for Athletic Injuries (C26.857.500.124), Anterior Cruciate Ligament Injuries Posterior Cruciate Ligament Tear, Rotator Cuff Injuries, Tibial Meniscus Injuries, Shoulder Dislocation or Subluxation is not yet recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here. | ||
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Clinical Outcomes of Arthroscopic Surgeries for Shoulder and Knee Sports Injuries (SK-COHORT) 500 Observational
Clinical Trial NCT07501013 (SK-COHORT) is an observational study for Athletic Injuries (C26.857.500.124), Anterior Cruciate Ligament Injuries Posterior Cruciate Ligament Tear, Rotator Cuff Injuries, Tibial Meniscus Injuries, Shoulder Dislocation or Subluxation and is currently not yet recruiting. Enrollment is planned to begin on April 1, 2026 and continue until the study accrues 500 participants. Led by Second Affiliated Hospital, School of Medicine, Zhejiang University, this study is expected to complete by April 1, 2046. The latest data from ClinicalTrials.gov was last updated on March 30, 2026.
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, ...
Show MoreDetailed Description
Despite significant advancements in arthroscopic techniques for shoulder and knee sports injuries (e.g., anterior cruciate ligament reconstruction, meniscus repair, and rotator cuff repair), postoperative clinical outcomes and return-to-sport rates remain highly variable among individuals. This variability is likely influenced by a complex interplay of patient baseline characteristics, specific tear morphologies, ind...Show More
Official Title
Clinical Outcomes and Associated Factors Following Arthroscopic Surgeries for Shoulder and Knee Sports Injuries: A Prospective Cohort Study
Conditions
Athletic Injuries (C26.857.500.124)Anterior Cruciate Ligament Injuries Posterior Cruciate Ligament TearRotator Cuff InjuriesTibial Meniscus InjuriesShoulder Dislocation or SubluxationOther Study IDs
- SK-COHORT
- 2025-1394
NCT ID Number
Start Date (Actual)
2026-04-01
Last Update Posted
2026-03-30
Completion Date (Estimated)
2046-04-01
Enrollment (Estimated)
500
Study Type
Observational
Status
Not yet recruiting
Keywords
Arthroscopy
Sports Medicine
Patient Reported Outcome Measures
Prospective Cohort
Clinical Outcomes
Sports Medicine
Patient Reported Outcome Measures
Prospective Cohort
Clinical Outcomes
Arms / Interventions
| Participant Group/Arm | Intervention/Treatment |
|---|---|
Shoulder Cohort Patients diagnosed with sports-related shoulder injuries (e.g., rotator cuff tear, shoulder instability) who are scheduled to undergo elective, standard-of-care shoulder arthroscopic surgery. | Standard of Care Shoulder Arthroscopy Routine, minimally invasive arthroscopic surgical procedures tailored to the patient's specific shoulder pathology, followed by standard postoperative rehabilitation. This is strictly observational; no experimental procedures are introduced. |
Knee Cohort Patients diagnosed with sports-related knee injuries (e.g., ACL rupture, meniscus tear) who are scheduled to undergo elective, standard-of-care knee arthroscopic surgery. | Standard of Care Knee Arthroscopy Routine, minimally invasive arthroscopic surgical procedures tailored to the patient's specific knee pathology, followed by standard postoperative rehabilitation. This is strictly observational; no experimental procedures are introduced. |
Primary Outcome Measures
Secondary Outcome Measures
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Patient-Reported Outcome Measures (PROMs) for Joint Function | Evaluation of joint function and symptoms using validated, standardized questionnaires. For the Knee Cohort, the International Knee Documentation Committee (IKDC) Subjective Knee Form will be used. For the Shoulder Cohort, the American Shoulder and Elbow Surgeons (ASES) score will be used. Higher scores indicate better joint function and less severe symptoms. | Preoperative baseline, 2 weeks, 1 month, 6 months, 1 year, and 2 years postoperatively. |
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Incidence of Postoperative Complications | Tracking the occurrence rate of any adverse events related to the surgery, including but not limited to surgical site infection, deep vein thrombosis (DVT), severe joint stiffness requiring manipulation, and graft failure or re-rupture requiring revision surgery. | From the date of surgery up to 2 years postoperatively. |
Pain Intensity Assessed by Visual Analog Scale (VAS) | Assessment of joint pain at rest and during activity using a 10-point Visual Analog Scale, where 0 represents "no pain" and 10 represents "worst imaginable pain." | Preoperative baseline, 2 weeks, 1 month, 6 months, 1 year, and 2 years postoperatively. |
Participation Assistant
Eligibility Criteria
Eligible Ages
Child, Adult, Older Adult
Minimum Age
8 Years
Eligible Sexes
All
- 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.
- 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 cooperation with follow-up.
- Patients in an involuntary state (e.g., under coercion).
- Refusal to sign the informed consent form or refusal to participate in the study.
- Currently participating in other interventional clinical trials that may confound or affect the clinical outcomes of this study.
Second Affiliated Hospital, School of Medicine, Zhejiang UniversityStudy Central Contact
Contact: Yan Xiong, Doctor, 0571-663553, [email protected]
No location data.