A Study on the Accuracy Evaluation of Vertebral Screw Insertion in Spinal Surgery Using Robot Assistance Guide

A comparative clinical study between prospective intervention group and retrospective cohort control group to evaluate the accuracy of pedicle screw insertion using robot-assisted guidance (CUVIS-spine) in spine surgery. (Investigator initiated trial, Multicenter study)

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0010607

Enrollment

206

Registered

2025-06-09

Start date

2025-06-16

Completion date

Unknown

Last updated

2025-06-24

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

Conditions

None listed

Interventions

Medical Device, Procedure/Surgery : This clinical study is a comparative clinical study between researchers-led multicenter, prospective intervention group, and retrospective cohort control group to c

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) men and women over the age of 19 2) A person who voluntarily agrees to participate in this study and is willing to comply with the research plan. 3) Diagnostic examination diagnosed with spinal (cervical, thoracic, or lumbar) degenerative spinal stenosis, degenerative and cavitary spinal anterior dislocation, vertebral deformation (spinal lumbar, scoliosis), degenerative and cavitary spinal anxiety, vertebral traumatic fractures, primary (or metastatic) spinal/spinal tumors, spinal/spinal infections, etc 4) Among the patients diagnosed in (3) above, those who need incision or percutaneous spinal cord screw insertion surgery.

Exclusion criteria

Exclusion criteria: 1) A person who has not agreed to maintain contraception during the clinical period if he/she is pregnant or lactating, or is a woman of childbearing age 2) If the researcher determines that participation in the clinical study is inappropriate because it may affect the results of other studies ethically or clinically

Design outcomes

Secondary

Measure	Time frame
Operative time;Intra operative blood loss;Hospital day	—

Primary

Measure	Time frame
GRS grade	—

Countries

Korea, Republic of

Contacts

Public ContactAra Ko

Yonsei University Health System, Severance Hospital

kosev@yuhs.ac+82-2-2228-0581

Outcome results