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Radiculopathy clinical trials

View clinical trials related to Radiculopathy.

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NCT ID: NCT06359470 Completed - Clinical trials for Disc Prolapse With Radiculopathy

the Modified Reversed Contralateral Axial Rotation Position

Start date: November 5, 2022
Phase: N/A
Study type: Interventional

This study aimed to investigate the effect of specific three-dimensional (3D) positions of the trunk on patients with lumbar discogenic pain with radiculopathy aiming to find a position that directly decompresses the impinged root as well as the effect of this position on the CSA of the L3-L4, L4-L5 and L5-S1 intervertebral foramen (IVF) using 3D-CT scan imaging of the real spine

NCT ID: NCT06335732 Completed - Clinical trials for Prevalence, Lumbosacral Radiculopathy

Prevalenc Of Lumbosacral Radiculopathy Among Physiotherapists Of Pediatric Rehabilitation OF PEDIATRIC REHABILITATION

Start date: December 5, 2022
Phase:
Study type: Observational

Determine the prevalence of lumbosacral radiculopathy among pediatric physiotherapists in the ministry of health in Cairo, Egypt.

NCT ID: NCT06240845 Completed - Clinical trials for Lumbar Radiculopathy

Effect of High Versus Low-level Laser Therapy in Patients of Lumber Radiculopathy

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

To Compare the effects of high-level laser therapy (HLLT) and low-level laser therapy (LLLT) on pain in patients with lumbar radiculopathy.

NCT ID: NCT06196385 Completed - Clinical trials for Cervical Radiculopathy

Efficacy Of Intensive Cervical Traction On Depression, Insomnia, Quality of Life In Patients With Cervical Radiculopathy

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

Cervical radiculopathy is a common and disabling condition involving local pain in the neck region and pain that radiates into the upper limb. Recent data suggest that cervical traction may effectively reduce disability and pain, with a dose-response relationship. The main aim of this study was therefore to evaluate the effect of an intensive cervical traction protocol for patients with cervical radiculopathy on depression, insomnia, and quality of life (1).

NCT ID: NCT06113263 Completed - Clinical trials for Cervical Radiculopathy

Anterior and Posterior Decompression Surgery in Individuals With Cervical Radiculopathy and Headache

Start date: January 1, 2014
Phase:
Study type: Observational [Patient Registry]

This is a prospective observational register-based cohort study with 2 years follow-up with data from the national Swedish Spine Register (Swespine). The aim is to study the differences between anterior and posterior decompression surgery on neck-related disability, headache, and neck- and arm pain in individuals with cervical radiculopathy and headache. Secondary, to study predictive factors for an improvement in neck-related disability, headache and neck- and arm pain after decompression srurgery. All individuals underwent either anterior or posterior decompression surgery and were operated between 2014-2021. Patient-reported data was collected preoperatively (baseline), and at 1- and 2-year follow-ups and surgeon-reported data regarding the operation were collected directly after the operation. Primary outcome is self-reported neck-related disability measured with Neck Disability Index and secondary outcomes are headache, measured with an item about headache of Neck Disability Index, and neck- and arm pain, measured with a 0 to 10-point numeric rating scale.

NCT ID: NCT06087107 Completed - Clinical trials for Lumbar Radiculopathy

Comparative Effects Of High Intensity Spinal Decompression Exercises And Eldoa In Patients Of Lumbar Radiculopathy

Start date: October 20, 2023
Phase: N/A
Study type: Interventional

To compare the effects of high intensity spinal decompression exercises and Eldoa on pain, ROM and Disability in patients of lumbar radiculopathy.

NCT ID: NCT06078163 Completed - Clinical trials for Sciatic Radiculopathy

Combined Rehabilitation With ALA, ALC, Resveratrol and Vitamin D in Discogenic Sciatica in Young People

Start date: July 1, 2022
Phase: N/A
Study type: Interventional

The objective of this Interventional case-control clinical study is to evaluate the effectiveness of physiotherapy combined with the administration of Alpha Lipoic Acid, L-acetylcarnitine, Resvelatrol, Vit D3 in the treatment of sciatica due to herniated disc in young patients. The main questions we intend to answer are: - Is this combined treatment more effective in reducing pain? - Is the combined treatment useful for improving postural alterations, reducing the intake of painkillers and the number of days of absence from work and improving the quality of life?

NCT ID: NCT06058806 Completed - Clinical trials for Lumbosacral Radiculopathy

Effects of Multimodal Physical Therapy in Patients With Lumbosacral Radiculopathy

Start date: June 1, 2018
Phase: N/A
Study type: Interventional

Purposes of the study To investigate the effect of Multimodal Physical Therapy on pain, daiablility H-reflex, and Diffusion Tensor Imaging (DTI) Parameters in Patients With Lumbosacral Radiculopathy.

NCT ID: NCT05959330 Completed - Clinical trials for Cervical Radiculopathy

Effects of Neural Tension Versus Neural Sliding Technique on Cervical Radiculopathy.

Start date: March 5, 2023
Phase: N/A
Study type: Interventional

The aim of this research is to find the effects of neural tension versus neural sliding technique on pain, cervical muscle endurance and hand grip strength in unilateral cervical radiculopathy. It will be a randomized controlled trial in which participants selected through non probability convenience sampling with age from 18 to 65 years having unilateral cervical radicular pain in upper limb since 3 months and any two of the following positive test Spurling's test, Distraction test and Upper Limb Tension Test. Participants will be randomly allocated, into three groups (A, B, and C). On the contrary, patients with any orthopedic or neurological conditions of cervical spine and shoulder joint, malignancy, cervical surgeries and bilateral cervical radiculopathies will be excluded from the study. Baseline measurement of all groups will be taken by using Numerical Pain Rating Scale (NPRS) for pain, Cranio-cervical Flexion Test for endurance and Hand-Held Dynamometer for hand grip strength. Group A will receive 7 neural tension technique, Group B will receive neural sliding technique, while Group C will receive both neural tension technique and neural sliding technique for 4 weeks (6 successive sessions). Both techniques (slider and tensioner) will be provided three sets in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment. SPSS 21 software will be used for data entry and analysis.

NCT ID: NCT05950321 Completed - Neck Pain Clinical Trials

Paramedian CESI vs Selective Nerve Root PRF for Lower Cervical Radicular Pain

Start date: August 1, 2022
Phase: N/A
Study type: Interventional

This study aims to compare the efficacy of ultrasound-guided selective cervical nerve root pulsed radiofrequency (PRF) versus fluoroscopy-guided paramedian cervical epidural steroid administration (CESI) for the treatment of lower cervical radicular pain refractory to conservative treatments. For this evaluation, a numerical rating (NRS), neck disability index (NDI), and Leeds Assessment Of Neuropathic Symptoms And Signs (LANSS) scale will be used before and after both interventions.