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Development and Clinical Translation of an AI-Intelligent Planning and Dynamic Registration System for Spinal Surgery Robots

Development and Clinical Translation of an AI-Intelligent Planning and Dynamic Registration System for Spinal Surgery Robots

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117725
Enrollment
Unknown
Registered
2026-01-28
Start date
2026-01-31
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Lumbar Disc Herniation

Interventions

Experimental group:AI algorithm-assisted spinal robotic pedicle screw placement surgery
Control group:Traditional free-hand pedicle screw placement

Sponsors

Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18–75 years (inclusive of the boundary values); 2.Seeking medical care at multi-center medical institutions including Sir Run Run Shaw Hospital, Affiliated to Zhejiang University School of Medicine (the leading unit of this study); 3.Diagnosed with lumbar disc herniation or lumbar spinal stenosis via MRI/CT, and meeting the indications for interbody fusion surgery; 4.No surgical contraindications such as severe hepatic or renal insufficiency, or coagulation dysfunction; 5.Able to cooperate with postoperative follow-up and relevant evaluations; 6.Voluntarily participate in this study and sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Having spinal deformity, osteoporosis, or a history of previous spinal surgery; 2.Complicated with severe systemic diseases (e.g., malignant tumors, severe cardiovascular diseases, immune system diseases, etc.); 3.Allergic to the instruments or materials used in the surgery; 4.Belonging to vulnerable groups, including patients with mental illness, cognitive impairment, critically ill patients, pregnant women, illiterates, etc. 5.Other circumstances deemed unsuitable for participation in this study by the researchers;

Design outcomes

Primary

MeasureTime frame
Screw Placement Accuracy;

Secondary

MeasureTime frame
Surgery-related indicators;Patient Satisfaction;Postoperative Recovery-related Indicators;Incidence of Adverse Events and Complications;

Countries

China

Contacts

Public ContactMa Jianjun

Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University

178746654@qq.com+86 571 86006687

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026