Ignite Creation Date:
2024-05-06 @ 8:13 PM
Last Modification Date:
2024-10-26 @ 3:22 PM
Study NCT ID:
NCT06290908
Status:
COMPLETED
Last Update Posted:
2024-03-04
First Post:
2024-02-20
Brief Title:
RPE-PTLIF for Lumbar Spinal Stenosis With Instability
Sponsor:
Wen-xi Sun
Organization:
Guangzhou University of Chinese Medicine
Study Overview
Official Title:
Robot-assisted Percutaneous Endoscopic PosteriorTransforaminal Lumbar Interbody Fusion for Lumbar Spinal Stenosis With Instability
Status:
COMPLETED
Status Verified Date:
2024-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Objective To analyze the effectiveness and safety of robot-assisted percutaneous endoscopic posteriortransforaminal lumbar interbody fusion RPE-PTLIF in the treatment of lumbar spinal stenosis with instability Methods A single-center prospective study from September 2018 to April 2022 patients with lumbar spinal stenosis and instability who met the inclusion and exclusion criteria were treated with RPE-PTLIF Pain visual analog scale VAS was used to evaluate the degree of low back pain and lower limb pain before operation 1 month 6 months 1 year after operation and at the final follow-up and the Oswestry disability index ODI was used to evaluate the degree of lumbar spinal function At the last follow-up MacNab criteria were used to evaluate the clinical efficacy Imaging evaluation included the measurement of intervertebral space height lumbar physiological curvature fusion rate and pedicle screw accuracy by preoperative and lateral X-ray films
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None