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Digital technology-assisted arthroscopy for precise and personalized treatment of anterior cruciate ligament injury: a randomized controlled trial.

Digital technology-assisted arthroscopy for precise and personalized treatment of anterior cruciate ligament injury

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000037284
Enrollment
Unknown
Registered
2020-08-27
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-10-13

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

Conditions

ACL injury

Interventions

Digital assistant group:Digital technology was used to assist in the formulation of preoperative plan and the operation was simulated before operation
Traditional solutions group:Preoperative preparation was carried out according to the traditional plan, and the operation plan was made after reading MRI

Sponsors

East Hospital of Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1) The above diagnostic criteria were met; 2) The age ranged from 18 to 40 years old; 4) Preoperative MRI showed that ACL injury was simple; 5) Patients who can tolerate surgical treatment; 6) The consciousness is clear, can complete to own pain judgment, appraisal pain cooperator; 7) They signed informed consent and volunteered to participate in the 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 joint operation history and obvious knee joint degeneration; 2) Patients with a history of major immunodeficiency or allergy to narcotic drugs; 3) For patients who were obviously rejected by surgery; 4) Cancer patients; 5) Patients with hemorrhagic diseases; 6) Patients with tuberculosis, hepatitis and other infectious diseases and patients with liver and kidney dysfunction; 7) Mental patients; All patients who met any of the above criteria were considered not suitable for inclusion in this study.

Design outcomes

Primary

MeasureTime frame
Knee range of motion;VAS degree;KSS degree;Bone tunnel changes;Operator satisfaction;

Countries

China

Contacts

Public ContactYuan Feng

East Hospital of Shanghai Sixth People's Hospital

yuanfeng@188.com+86 13917819693

Outcome results

None listed

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