NCT07885943

Brief Summary

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for all trials

Timeline
15mo left

Started Jan 2024

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress70%
Jan 2024Jan 2028

Study Start

First participant enrolled

January 1, 2024

Completed
2.8 years until next milestone

First Submitted

Initial submission to the registry

October 14, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

October 21, 2026

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2028

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2028

Last Updated

October 21, 2026

Status Verified

October 1, 2026

Enrollment Period

4 years

First QC Date

October 14, 2026

Last Update Submit

October 14, 2026

Conditions

Keywords

Meniscus regeneration; Magnetic Resonance Imaging (MRI); Three-dimensional reconstruction; Volume quantification; Cohort study.

Outcome Measures

Primary Outcomes (1)

  • Percentage of regenerated volume of the partially resected meniscus after 6 months and 1 year post-surgery.

    Six months and one year post-surgery.

Secondary Outcomes (1)

  • Knee joint function assessment score.

    Six months and one year post-surgery.

Study Arms (4)

Partial meniscectomy.

Patients who underwent partial meniscectomy at our hospital.

Other: No intervention measures.

Complete resection of the meniscus.

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 resection of the meniscus + drilling of a bone channel.

Complete meniscectomy + anterior cruciate ligament reconstruction with drilling of an osteotomy channel.

Other: No intervention measures.

Partial meniscectomy + drilling of a bone channel.

Performed a partial meniscectomy + anterior cruciate ligament reconstruction with drilling of an osteotomy channel.

Other: No intervention measures.

Interventions

No intervention measures.

Complete resection of the meniscus + drilling of a bone channel.Complete resection of the meniscus.Partial meniscectomy + drilling of a bone channel.Partial meniscectomy.

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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.

You may qualify if:

  • Patients who underwent partial resection of the meniscus using arthroscopy in our hospital and had follow-up thin-slice MRI scans within one week after surgery; no cases of joint infection, joint tumors, or other diseases were present.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tsinghua Changgung Hospital, Beijing

Beijing, Beijing Municipality, 410006, China

RECRUITING

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Target Duration
1 Year
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 14, 2026

First Posted

October 21, 2026

Study Start

January 1, 2024

Primary Completion (Estimated)

January 1, 2028

Study Completion (Estimated)

January 1, 2028

Last Updated

October 21, 2026

Record last verified: 2026-10

Locations