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Radicular Pain clinical trials

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NCT ID: NCT05747807 Recruiting - Clinical trials for Disk Herniated Lumbar

Percutaneous Intradiscal Radiofrequency as A Treatment for Radicular Pain From Lumbar Disc Herniation

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to demonstrate the efficacy of percutaneous intradiscal radiofrequency as a treatment for radicular pain from lumbar disc herniation. The main question it aims to answer is: • Can percutaneous intradiscal radiofrequency lower the severity of radicular pain from lumbar disc herniation Participants will be treated with percutaneous intradiscal radiofrequency and evaluated for radicular pain severity before and 3 months after the procedure. There is no comparison group.

NCT ID: NCT05632835 Not yet recruiting - Low Back Pain Clinical Trials

Application of 3D Printing Guide Plate in Endoscopic Spinal Surgery

Start date: November 25, 2022
Phase: N/A
Study type: Interventional

Application of 3D printing guide plate in endoscopic spinal surgery

NCT ID: NCT05610553 Not yet recruiting - Low Back Pain Clinical Trials

Application of 3D Printing Guide Plate in Percutaneous Disc Decompression

Start date: December 10, 2022
Phase: N/A
Study type: Interventional

Application of 3D printing guide plate in percutaneous disc decompression

NCT ID: NCT05487690 Not yet recruiting - Low Back Pain Clinical Trials

Application of 3D Printing Guide Plate in Spinal Minimally Invasive and Interventional Surgeries

Start date: October 20, 2022
Phase: N/A
Study type: Interventional

Application of 3D printing guide plate in spinal minimally invasive and interventional surgeries

NCT ID: NCT01205464 Completed - Fatigue Clinical Trials

Effects of Doxycycline on Persistent Symptoms Post-neuroborreliosis

Start date: February 2005
Phase: N/A
Study type: Interventional

The aim of this randomised, double-blind crossover study was to determine whether Doxycycline has an impact on the persistent symptoms post-neuroborreliosis, through alterations in the immune response and whether such an effect could influence the clinical outcome.

NCT ID: NCT00880828 Active, not recruiting - Clinical trials for Cervical Radiculopathy

Comparing Two Different Cervical Collars for the Treatment in Patient With Cervical Radiculopathy and Radicular Pain

Start date: August 2010
Phase: N/A
Study type: Interventional

The primary objective of the study is to investigate the efficacy of device with far-infrared (FIR) irradiation in these patients with acute cervical radiculopathy.

NCT ID: NCT00516009 Recruiting - RADICULAR PAIN Clinical Trials

Efficacy of Intravenous Dexamethasone for Acute Disc Herniation-Induced Sciatica

Start date: August 2007
Phase: N/A
Study type: Interventional

Acute low back pain is one of the most common reasons for all physician visits(1). Phospholipase A2 (PLA2), a potent inflammatory mediator, has demonstrated to be released by discs following injury(4). Clinical practice and animal research suggest that lumbar radicular pain is the result of inflammation of the nerve root in the epidural space(5). The study will evaluate the efficacy of intravenous Dexamethasone for acute disc herniation-induced sciatica. 40 patients aged 18 years or older, who will be transferred to the emergency room due to sciatic pain will be blindly randomized to receive Dexamethasone 30 mg IV for 3 days an tapering off, 10 mg daily, or normal saline. 20 patients will be in each group. The patients will continue their standard care during the study period. Follow up will last for 3 months. Mann-Whitney test will be used for parametric correlation, Wilcoxon for numeral and x² for categorial variables. Dexamethasone IV can help physicians in treating patients with acute sciatic pain.

NCT ID: NCT00189605 Completed - Radicular Pain Clinical Trials

Prospective, Randomized, Multi-center Clinical Study of Plasma Disc Decompression

SPINE
Start date: September 2004
Phase: Phase 4
Study type: Interventional

The goal of this post-marketing surveillance study is to compare two procedures which are used to treat patients who require a disc decompression procedure. These procedures are: 1) plasma disc decompression procedure using Coblation technology and 2) fluoroscopy guided transforaminal epidural steroid injection (TFESI). The study will evaluate treatment efficacy and rate of improvement in symptoms through the first six months following the procedure. The principal objectives of this study are to determine whether subjects receiving the plasma disc decompression procedure demonstrate: 1. Improved clinical outcomes over subjects receiving TFESI 2. More rapid reversal of symptoms than subjects receiving TFESI