Clinical Trials Logo

Radiculopathy clinical trials

View clinical trials related to Radiculopathy.

Filter by:

NCT ID: NCT05258214 Completed - Clinical trials for Lumbar Radiculopathy

Mulligan BLR Versus Mulligan TSLR Versus Neural Mobilization n Patient With Lumber Radiculopathy

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

The goal of this study is to compare the effectiveness of mulligan traction Straight Leg Raise and mulligan's bent leg rise and neural mobilization to conventional therapies in order to assess which treatment is more successful in treating lumbar radiculopathy-related dysfunction.

NCT ID: NCT05234268 Completed - Clinical trials for Cervical Radiculopathy

Cervical Traction, Passive Accessory Intervertebral Movements and Active Strength Training in Cervical Radiculopathy

Start date: June 30, 2021
Phase: N/A
Study type: Interventional

To determine the effectiveness of Manual Cervical Traction, Passive Accessory Intervertebral Movements (PAIVMs) and Active strength training in the management of cervical radiculopathy. To compare the effectiveness of Manual Cervical Traction, Passive Accessory Intervertebral Movements (PAIVMs) and Active strength training in the management of cervical radiculopathy.

NCT ID: NCT05191537 Completed - Clinical trials for Radiculopathy, Cervical

Spinal Mobilization With Arm Movement and Positional SNAGS in Cervical Radiculopathy Patients

Start date: December 1, 2021
Phase: N/A
Study type: Interventional

Data will be collected in Hussain Memorial Hospital by taking informed consent. Randomised clinical trial is conducted taking thirty patients of both genders with confirmed diagnoses of cervical radiculopathy, their ages ranged from 25 to 60. A cluster of winner to rule out patient with cervical radiculopathy. They will be randomly assigned into two groups by the lottery method. Group A will receive conventional treatment and of spinal mobilization with arm movement (intervention 1) Group B will receive conventional treatment and positional SNAGs (intervention 2). The treatment will be conducted at a frequency of three sessions per week for four weeks. Two values will be taken, one as baseline and the other at end of the session. Then follow up the patient to rule out which intervention is more effective than the other. Neck Disability Index, Numeric Pain Rating Scale and ROM will be used to measure outcomes.

NCT ID: NCT05145842 Recruiting - Spinal Stenosis Clinical Trials

The Effect of Combination of Ultrasound and Flouroscopy Guidance in Caudal Epidural Injections

Start date: May 26, 2021
Phase: N/A
Study type: Interventional

The primary purpose of this study is to asses the effect of caudal epidural injection guided by a combination of ultrasound and fluoroscopy on the duration of the procedure and the amount of radiation exposed during the procedure, compared to the application of only fluoroscopy-guided. Secondary aims are to reveal the presence of structural variations that prevent injection by examining the morphology of the sacral hiatus by ultrasonography.

NCT ID: NCT05115461 Enrolling by invitation - Neuropathic Pain Clinical Trials

Neuropathic Pain and Postural Stability in Patients With Lumbar Radiculopathy

Start date: November 10, 2021
Phase:
Study type: Observational [Patient Registry]

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?

NCT ID: NCT05099796 Completed - Low Back Pain Clinical Trials

Epidural Steroid Injections in Post-lumbar Surgery Syndrome After Single-level Discectomy

Start date: January 5, 2016
Phase: N/A
Study type: Interventional

62 patients with postlumbar surgery syndrome were randomized and divided into two groups. Transforaminal epidural steroid injection (TFESI) was applied to the TFESI group (n=31), and caudal epidural steroid injection (CESI) was applied to the CESI group (n=31). The age of the patients involved in this study ranged from 18 years old to 65 years old

NCT ID: NCT05088954 Recruiting - Metabolic Syndrome Clinical Trials

Effect of Metabolic Syndrome on Outcomes of Transforaminal Epidural Steroid Injection Treatment in Chronic Lumbar Radiculopathy

Start date: September 1, 2021
Phase: N/A
Study type: Interventional

Transforaminal epidural steroid injection (TFESI) has been increasingly preferred in patients who can not benefit from conservative approach in the treatment of lumbosacral radiculopathic pain due to lumbar disc herniation. The aim of our study is to evaluate the effect of metabolic syndrome on the treatment results of transforaminal epidural steroid injection in patients with chronic radicular low back pain due to lumbar disc herniation.

NCT ID: NCT05082220 Completed - Pain Clinical Trials

Analysis of Spread Level During Thoracic Erector Spinae Block

Start date: February 21, 2022
Phase: N/A
Study type: Interventional

The primary purpose of this study was to identify the ESPB spread level in the craniocaudal direction when performed at the T2 level. The secondary purpose was to determine the incidence of spread into epidural, paravertebral, intercostal, and intravascular injections with ESPB

NCT ID: NCT05066711 Enrolling by invitation - Clinical trials for Cervical Radiculopathy

NuVasive® ACP System Study

Start date: May 22, 2022
Phase:
Study type: Observational

The primary objective of this study is to evaluate the safety and performance of anterior cervical spine surgery using the NuVasive anterior cervical plate (ACP) System as measured by reported complications, radiographic outcomes, and patient-reported outcomes (PROs).

NCT ID: NCT05059249 Completed - Low Back Pain Clinical Trials

Effects of Mechanical Versus Manual Traction in the Management of Low Back Pain.

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

This study compared the effects of mechanical and manual traction on pain, disability and lumbar spinal curvature in patients with discogenic low back pain