An observational study in Meniscus Regeneration and Partial Meniscectomy, sponsored by Beijing Tsinghua Chang Gung Hospital. Recruiting at 1 site in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-10-21.
Sponsored by Beijing Tsinghua Chang Gung Hospital · Observational
This study aims to employ 3.0T thin-slice high-resolution magnetic resonance imaging (MRI) and MIMICS image three-dimensionalreconstruction.Additionally, we examined the regeneration of the menisci in patients who had undergone partial meniscectomy of the knee joint at our hospital through retrospective follow-up and meniscus segmentation techniques.
Proactive quantitative analysis of the meniscus in patients following partial meniscectomy of the knee joint 6 months and 12 months post-surgery.
The relationship between the percentage of regenerated tissue and the location and extent of the surgical excision.
1 Research Objectives
Primary objectives: Quantitatively determine the percentage of meniscal regeneration in patients 6 months and 12 months post-surgery; evaluation.
Identify the primary factors that influence or determine the regeneration of tissues, and explore clinical factors that may impact regeneration outcomes, such as age.The extent of the excision, the location of the excision, the inner or outer meniscus, and the degree of osteoarthritis, among other factors.
Provides references for the selection of surgical methods.
The ratios reveal the relationship between structural repair and functional improvement.
2. Content of the Study The content of this study was based on a follow-up observation of patients who underwent partial meniscectomy at our hospital over a period of six months and one year after surgery.Thin-layer magnetic resonance imaging data acquisition, MIMICS image three-dimensional reconstruction and segmentation, precise quantification, and statistical analysis verification.Explore the decisive factors influencing meniscus regeneration.
3.Research design. This study is a bi-directional cohort study; it is a single-center study conducted in a single-blind format.
4. Research Subjects For patients who have undergone partial meniscectomy using arthroscopy at our hospital, as well as those planning to undergo a similar procedure at our facility.Patients who have undergone a surgical procedure.
5. Eligibility Criteria Patients who underwent partial resection of the meniscus using arthroscopy at our hospital and had follow-up thin-slice MRI scans within one week after surgery.Absence of joint infections, joint tumors, and other diseases that require joint fusion.
6. Exclusion Criteria Patients who did not undergo an MRI scan within one week after surgery for the removal of the inferior meniscus using arthroscopy, who had MRI scan contraindications or refused the procedure.
Patients who underwent nuclear magnetic resonance (NMR) re-evaluation and had undergone surgery at least half a year prior to the commencement of this experiment.
7. Intervention Methods This study is an observational study, and no additional therapeutic interventions were applied.
8. Observation indicators and follow-up plan Observation indicator: The volume of meniscus regeneration measured through MRI 3D reconstruction at 6 months and 12 months post-surgery.
The results were compared to the volume of the meniscus at 1 week post-surgery. Additionally, a functional assessment of the knee joint (WOMET) was performed at corresponding time points.
Scoring tools, Lysholm scoring scale). Follow-up plan: Patients will be notified by phone to return to the hospital for a follow-up MRI examination 6 months and 12 months after surgery, during which their knee function will be evaluated.
The nuclear magnetic resonance (NMR) results were imported into MIMICS for image segmentation and reconstruction.
9. Statistical analysis methodology
. Data description and collation
. Analysis of key outcome indicators
Assess its long-term stability. If the overall difference is significant, a second-to-second comparison will be made.
. Analysis of secondary outcome indicators
. Explore Analysis
. Statistical software and significance level
Beijing Tsinghua Chang Gung Hospital is the lead sponsor of 102 studies on the registry; 52 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Research Subjects For patients who have undergone partial meniscectomy using arthroscopy at our hospital, as well as those planning to undergo a similar procedure at our facility.
Patients who have undergone a surgical procedure.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Patients who underwent nuclear magnetic resonance (NMR) re-evaluation and had undergone surgery at least half a year prior to the commencement of this experiment.
Patients who underwent partial meniscectomy at our hospital.
Other: No intervention measures.
Patients who have undergone a complete resection of the meniscus due to a discoid meniscus or meniscal tear at our hospital.
Other: No intervention measures.
Complete meniscectomy + anterior cruciate ligament reconstruction with drilling of an osteotomy channel.
Other: No intervention measures.
Performed a partial meniscectomy + anterior cruciate ligament reconstruction with drilling of an osteotomy channel.
Other: No intervention measures.
No intervention measures.
Percentage of regenerated volume of the partially resected meniscus after 6 months and 1 year post-surgery.
Time frame: Six months and one year post-surgery.
Knee joint function assessment score.
Time frame: Six months and one year post-surgery.
Started Jan 2024 (actual). Primary completion is estimated for Jan 2028, 48 months after the start.
How these figures are worked out, and which studies are left out of them.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.
Contact study teamGet an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Beijing Tsinghua Chang Gung Hospital →