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Lumbar Radiculopathy clinical trials

View clinical trials related to Lumbar Radiculopathy.

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NCT ID: NCT04547075 Completed - Clinical trials for Patient Satisfaction

In Turkish Version Lumbar Spine Surgery Expectation Survey

Start date: February 15, 2021
Phase:
Study type: Observational

The aim of this study was to determine the Turkish validity and reliability of Lumbar Spine Surgery Expectations Survey developed by Mancuso.

NCT ID: NCT04540068 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Prediction of TEI Success in Sciatica

POTEISS
Start date: November 15, 2020
Phase:
Study type: Observational

Rationale: Treatment with transforaminal epidural injections is part of usual care in patients suffering from lumbar radiculopathy. However, not all patients experience a satisfactory result from this treatment and it is unclear what percentage of patients responds well and if any clinical or radiological factors exist that predict a positive response. Objectives: Primary: to develop a model based on demographic, clinical and radiological parameters for prediction of treatment success after TEI Secondary: to estimate the short-term efficacy of TEI in patients with LDH and spinal stenosis based on pain, functionality and perceived recovery scores, to determine the correlation between clinical and radiological baseline parameters and physical and psychological patient outcome measures, to determine the rate of additional injections and rate of surgery after treatment with TEI, to determine the short-term (cost)effectiveness of TEI on physical and psychological patient outcome measures, and to determine the rate of complications associated with TEI Study design: Prospective cohort study Study population: Patients that are scheduled for TEI as part of usual care suffering from a new episode of lumbar radiculopathy Main study parameters/endpoints: leg and back pain scores at baseline, 30 minutes, 2 and 6 weeks after treatment. ODI, HADS, Quality of Life and PCI at baseline, 2 and 6 weeks after treatment. Perceived recovery at 2 and 6 weeks after treatment. Usage of healthcare at baseline, 2 and 6 weeks after treatment.

NCT ID: NCT04507113 Recruiting - Clinical trials for Magnetic Resonance Imaging

Diffusion Tensor (DTI) for the Assessement of Therapeutic Evolution of Patients With Acute Lumbar Radiculalgia

DiTi-Aïe
Start date: April 6, 2022
Phase: N/A
Study type: Interventional

Diffusion tensor imaging (DTI) is a non-invasive MRI technique offering a functional approach that provides morphological information about the microstructures of the nerve roots. DTI is a widely used neuroimaging technique and is a current topic of research in the field of peripheral nerve imaging.The aim of the study is to determine the prognostic quality of the DTI parameters to predict the therapeutic evolution of patients with lumbar radiculalgia at 6 months.

NCT ID: NCT04427423 Completed - Clinical trials for Lumbar Radiculopathy

Positional Distraction and Stabilization Exercises in Adults With Lumbar Radiculopathy.

Start date: April 10, 2020
Phase: N/A
Study type: Interventional

This study evaluate the addition of positional distraction to stabilization exercises in the treatment of lumbar radiculopathy in adults. Half of the patients will recieve positional distraction and stabilization exercises in combination, while the other half will recieve stabilization exercises only.

NCT ID: NCT04212949 Recruiting - Clinical trials for Lumbar Radiculopathy

The Effect of Transcranial Magnetic Stimulation Therapy in Patients With Lumbar Radiculopathy

Start date: November 8, 2019
Phase: N/A
Study type: Interventional

The present study aims to investigate the efficacy of repetitive transcranial magnetic stimulation of the motor cortex combined with transforaminal epidural steroid injection in patients with chronic lumbar radiculopathy.

NCT ID: NCT04042948 Completed - Clinical trials for Lumbar Spinal Stenosis

Clinical Effect of Preventive Use of Tylenol on Fever After Removal of Drainage Tube in Lumbar Fusion Surgery

Start date: June 24, 2019
Phase: N/A
Study type: Interventional

This study evaluates the influence of Non-steroidal Anti-inflammatory Drugs on preventing fever after the removal of drainage tube in the patients who suffered lumbar fusion surgery, if the outcome turn out positive, the preventive use of non-steroidal anti-inflammatory drugs could decrease the possibility of fever happening when we remove the tube.

NCT ID: NCT03952377 Terminated - Clinical trials for Lumbar Radiculopathy

Safety and Efficacy of SX600 Administered by Lumbosacral Transforaminal Epidural Injection for Radicular Pain

SALIENT
Start date: November 4, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

This is a Phase I/II, double-blind, parallel-group, randomized, placebo-controlled multi-centre trial in 180 patients randomized 1:1:1 to receive the IMP (Dexamethasone acetate microspheres for extended-release injectable micro-suspension, SX600 at 12.5 mg or 25.0 mg) or Placebo (0.9% Sodium Chloride for Injection, BP) via transforaminal epidural injection to the lumbosacral epidural space.

NCT ID: NCT03733626 Active, not recruiting - Clinical trials for Degenerative Disc Disease

Clinical Outcomes Associated With the Use of ViviGen® for the Treatment of Lumbar Degenerative Disc Disease

ViviGen
Start date: March 19, 2019
Phase: N/A
Study type: Interventional

The objective of this study is to perform a prospective, randomized, controlled clinical trial to compare radiographic fusion rates and patient reported outcomes, including pain and function preoperatively and postoperatively, using Depuy ViviGen® Cellular Bone Matrix mixed with cortical/cancellous allograft in conjunction with an approved Depuy Synthes pedicle screw system compared to autograft mixed with cortical/cancellous allograft in conjunction with the same DePuy Synthes pedicle screw system used for a one or two - level posterolateral lumbar fusion.

NCT ID: NCT03620864 Completed - Clinical trials for Lumbar Radiculopathy

Neurodynamic Intervention for Lumbar Radiculopathy

Start date: August 10, 2018
Phase: N/A
Study type: Interventional

Low back pain (LBP) is a common condition and has a significant impact on the individual in terms of pain and disability. Lumbar radiculopathy occurs often with LBP and may be the result of a lumbar herniated disc which will irritate a lumbar nerve trunk resulting in intraneural inflammation. There is evidence supporting the use of manual therapies of lumbar radiculopathy. One potential manual therapy is neurodynamic mobilization technique. No scientific evidence, based on a RCT, exists that this particular approach is beneficial for individuals with LBP and lumbar radiculopathy

NCT ID: NCT03543033 Withdrawn - Clinical trials for Lumbar Radiculopathy

Preoperative Corticosteroid Epidural Injection and Lumbar Decompression Surgery Outcomes

Start date: September 10, 2018
Phase: N/A
Study type: Interventional

This randomized control trial will compare opioid use, pain, and functional outcomes following decompression surgery for single-level lumbar radiculopathy in patients who undergo placement of corticosteroid epidural injection within 2 weeks prior to surgery compared to those who do not. The hypothesis of this study is that patients who receive the preoperative corticosteroid injection will have less reduced postoperative opioid use, as well as earlier mobilization, reduced length of stay, and faster return to work compared to control patients who do not receive the injection.