Viewing Study NCT05115461


Ignite Creation Date: 2025-12-24 @ 12:49 PM
Ignite Modification Date: 2025-12-28 @ 6:02 PM
Study NCT ID: NCT05115461
Status: ENROLLING_BY_INVITATION
Last Update Posted: 2024-11-04
First Post: 2021-11-01
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Neuropathic Pain and Postural Stability in Patients With Lumbar Radiculopathy
Sponsor: Bozyaka Training and Research Hospital
Organization:

Study Overview

Official Title: Postural Stability in Patients With Lumbar Radiculopathy and it's Relation to Neuropathic Pain: a Cross Sectional Case-control Study
Status: ENROLLING_BY_INVITATION
Status Verified Date: 2024-10
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: The aim of this study is to answer the questions below;

1. Is there a difference between patients with lumbar radiculopathy suffering from radicular pain and healthy subjects in terms of static and dynamic postural stability?
2. Is there a relationship between postural stability and the neuropathic characteristics of radicular pain?
Detailed Description: Patients presenting to our outpatient clinic with radicular pain and MRI findings associated with radiculopathy will be tested for static and dynamic postural stability. Patient demographics, pain intensity, neuropathic pain scores, and level of disability will also be recorded. The demographic data and postural stability scores will also be collected for the control subjects. Differences between the patient and control groups in terms of postural stability parameters will be sought. In addition, the relationship between the variables representing balance in the patient group and the neuropathic pain score and disability will be investigated.

Study Oversight

Has Oversight DMC: False
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?: