Viewing Study NCT06407167



Ignite Creation Date: 2024-05-11 @ 8:30 AM
Last Modification Date: 2024-10-26 @ 3:29 PM
Study NCT ID: NCT06407167
Status: RECRUITING
Last Update Posted: 2024-05-31
First Post: 2024-04-24

Brief Title: Neuropathic Pain in Patients With Degenerative Lumbar Stenosis
Sponsor: NN Priorov National Medical Research Center of Traumatology and Orthopedics
Organization: NN Priorov National Medical Research Center of Traumatology and Orthopedics

Study Overview

Official Title: Observational Cohort Study of the Neuropathic Pain in Surgical Treatment of Patients With Degenerative Lumbar Stenosis
Status: RECRUITING
Status Verified Date: 2024-05
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: Pre- and postoperative pain in patients with degenerative stenosis requires great attention as it can mislead the doctor about treatment tactics Neuropathic pain in the legs before and after the surgical procedure as well as the residual or recurrent pain syndrome existing against this background overshadow the patients recovery and cast doubt on the fullness of the performed decompression Neural compression in the spinal canal and back pain may be the cause of the patients antalgic posture and sagittal imbalance as seen on X-Ray to need for corrective interventions surgical procedure

Thus it is necessary to clarify the role and the influence of the pain and its type on the perioperative period in patients with degenerative lumbar spinal stenosis
Detailed Description: The current study is prospective observational study to evaluate the role of pain syndrome including neuropathic pain in surgical outcomes in patients with degenerative lumbar spinal stenosis

This study will be conducted at Priorov Central Institute for Trauma and Orthopedics Moscow Russia

The study is expected to enroll at least 120 adult patients with degenerative lumbar stenosis The neuropathy will be assessed preoperatively and then the patient will undergo decompressive lumbar surgery without fusion

The neuropathic pain will be evaluated according to DN4 preoperatively each patient will be assigned to one of two groups depending on the total value of DN4 - with the presence of neuropathy DN4 4 and without neuropathy DN4 4

Postoperative evaluation will include 2 visits during one year to evaluate clinical and radiological outcomes

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