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Precise, standardized and personalized application and promotion of digital technology assisted ACL double bundle eight strand anatomical reconstruction therapy

Precise, standardized and personalized application and promotion of digital technology assisted ACL double bundle eight strand anatomical reconstruction therapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047115
Enrollment
Unknown
Registered
2021-06-08
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

anterior cruciate ligament injure

Interventions

Control group:Preoperative preoperative evaluation method was used, and preoperative physical examination and MRI image reading were used to formulate the surgical plan
Experimental group:The femoral intercondyle, tibial plateau and patella were reconstructed on the 3D image of knee joint made by MIMICS software using digital technology

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18 to 40 years; 2.Preoperative MRI showed that ACL injury was simple; 3.Can tolerate surgical treatment; 4.Clear consciousness, able to complete their own pain judgment, evaluation of pain collaborators; 5.Signed informed consent and volunteered to participate in this study. All the above standards must be met before they can be included in this test.

Exclusion criteria

Exclusion criteria: 1.Patients with previous knee surgery history and obvious knee degeneration; 2.Patients with a history of major immunodeficiency or allergic to narcotic drugs; 3.Cancer patients; 4.Patients with hemorrhagic diseases; 5.Patients with tuberculosis, hepatitis and other infectious diseases and liver and kidney dysfunction; 6.Psychotic patients. All patients who met any of the above criteria were considered unsuitable for inclusion in this study.

Design outcomes

Primary

MeasureTime frame
Visual simulation of pain scale;Knee motion score;Computed tomography;Range of motion (flexion, extension) and Joint Stability (KT-2000);Muscle status measurement;

Countries

China

Contacts

Public ContactYuan Feng

Shanghai Sixth People's Hospital

zcy157@163.com+86 21 38297510

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026