Application of 3D Printing Guide Plate in Endoscopic Spinal Surgery
1 other identifier
interventional
28
1 country
1
Brief Summary
Application of 3D printing guide plate in endoscopic spinal surgery
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Nov 2022
1 active site
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
First Submitted
Initial submission to the registry
October 29, 2022
CompletedStudy Start
First participant enrolled
November 25, 2022
CompletedFirst Posted
Study publicly available on registry
December 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2023
CompletedDecember 1, 2022
September 1, 2022
9 months
October 29, 2022
November 20, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
C-arm fluoroscopy times
Numbers of using C-arm fluoroscopy
Intraoperative
Secondary Outcomes (4)
Puncture time
Intraoperative
Numerical rating scale
Postoperative 1 day, 2 weeks, 1 month
Patient satisfaction
Postoperative 1 months
Rate of Complications
Intraoperative
Study Arms (2)
3D printing guide plate group
EXPERIMENTAL3D-printed customized guide plate will be used to guide the puncture in endoscopic spinal surgeries.
Conventional guidance group
ACTIVE COMPARATORThe surgeons would place the needle according to his/her previous experience under the guidance of C-arm fluoroscopy or CT.
Interventions
3D-printed customized guide plate will be used to guide the puncture in endoscopic spinal surgeries to help to reduce intra-operative radiation, puncture time, etc..
The surgeons would place the needle according to his/her previous experience under the guidance of C-arm fluoroscopy or CT.
Eligibility Criteria
You may qualify if:
- Age ≥18 years old;
- Pain lasting ≥12 weeks;
- The previous failure of conservative management such as physiotherapy, exercise therapy, or analgesic medications;
- Pain intensity≥4 out of 10 on the numerical rating scale (NRS);
- Availability of computed tomography/magnetic resonance imaging findings of pathology concordant with the side and level of their clinical features;
- Agree with endoscopic spinal surgeries.
You may not qualify if:
- Patient refusal to participate in the study;
- Pregnant or nursing;
- Allergies to local anesthetics, contrast dyes or steroids;
- Significant anatomic deformity (either congenital or acquired) making it difficult to access the target as evidenced by computed tomography/magnetic resonance imaging;
- Patients with platelet dysfunction, bleeding disorder or continuing anticoagulant treatment;
- Systemic infection;
- Injection site infection;
- Unstable medical or psychiatric condition;
- Unable to tolerate the surgeries.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Pain medicine center of Peking University Third Hospital
Beijing, Beijing Municipality, 100191, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 29, 2022
First Posted
December 1, 2022
Study Start
November 25, 2022
Primary Completion
August 31, 2023
Study Completion
December 31, 2023
Last Updated
December 1, 2022
Record last verified: 2022-09
Data Sharing
- IPD Sharing
- Will not share