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Cervical Spondylosis clinical trials

View clinical trials related to Cervical Spondylosis.

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NCT ID: NCT04544683 Completed - Clinical trials for Cervical Radiculopathy

Effectiveness of Cervical Transforaminal Epidural Steroid Injection

Start date: October 23, 2018
Phase: Phase 4
Study type: Interventional

Study Purpose: This study is intended to monitor outcomes for 1 year following cervical TFESI. Based on current clinic volume and enrollment rates into a current study of cervical epidural injections that is nearing completion, we conservatively estimate a study enrollment period of 18 months and a total period of 2.5 years from enrollment to final follow-up data collection. If the study were to theoretically start enrolling in July 2019, we would anticipate completion by February 2022. Objectives: 1. Determine the proportion of patients with an 80% or greater improvement in arm and neck numerical rating scale pain (NRS) score following an initial cervical transforaminal steroid injection (TFESI) at 4 weeks post-injection and the duration of response up to 12 months. 2. Determine the proportion of patients with a 50%-79% improvement in arm and neck NRS score following an initial cervical TFESI at 4 weeks post-injection and the duration of response up to 12 months. 3. Determine the proportion of patients with less than 50% improvement in arm and neck NRS score following an initial cervical TFESI at 4 weeks post-injection and the duration of response up to 12 months. 4. Determine the proportion of patients with an initial injection plus up to 3 additional injections that maintain 80% or greater, as well as 50-79%, improvement in arm and neck NRS score for up to 12 months. 5. Determine the proportion of patients with a clinically significant change in function defined by a minimally clinically significant change (MCIC) (≥10 point improvement ) or 30% improvement in Neck Disability Index (NDI) score following an initial cervical TFESI at 4 weeks post-injection and the duration of response up to 12 months. 6. Determine the proportion of patients with clinically significant improvement in the Medication Quantification Scale (MQS III) score (≥6.8 point change , equivalent to 10 oral morphine equivalents ) following an initial cervical TFESI at 4 weeks post-injection and the duration of response up to 12 months. 6. Determine the proportion of patients with clinically significant improvement in the categorical EuroQol 5 Dimensions tool (EQ-5D) defined by ≥0.03 following an initial cervical TFESI at 4 weeks post-injection and the duration of response up to 12 months. 7. Compare patient demographic, clinical, and imaging characteristics between response groups and perform predictive modeling to better understand variables that increase the likelihood of a successful clinical outcome. 8. Report adverse effects.

NCT ID: NCT04525651 Recruiting - Clinical trials for Cervical Spondylosis

Clinical Evaluation for Digital Acupuncture Manipulation Therapeutic Instrument

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

The investigators design a randomized, control study to evaluate the therapeutic effect of digital acupuncture instrument in cervical spondylotic radiculopathy patients using the following outcomes: the Visual analogue scale(VAS), neck disability index scale (NDI) and short form 36-item questionnaire (SF-36).

NCT ID: NCT04489394 Completed - Trauma Clinical Trials

Quintex® Follow-up After One Year Minimum

Quintex
Start date: November 11, 2019
Phase:
Study type: Observational

Prospective study, not randomised, non-interventional, monocentric, investigating an intended patient cohort of 60 patients already operated on the cervical spine due to degenerative disc disease of the cervical spine down to the first thoracolumbar VBR (C2-T1), who received a Quintex plate for stabilisation

NCT ID: NCT04287634 Completed - Clinical trials for Cervical Spondylosis

Comparison Between the Segmental Mobilization and Entire Segmental Spine Mobilization in Cervical Spondylosis

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

All the patients of cervical spondylosis which were enrolled in this study were assessed in Rehabilitation centre of Yusra General Hospital. Patients who compete the inclusion criteria are randomly assigned by the seal envelop method in to two groups interventional and control group. There is nine sessions of three weeks rehabilitation program and Pain is assessed on Numeric pain rating scale, Disability on Neck Disability index and ROM is assessed by Goniometer in 1ST, 4TH and last visit. Three sessions of intervention is given to patient per week.

NCT ID: NCT04113473 Completed - Neck Pain Clinical Trials

An Evaluation of Yoga Therapy for Cervical Spondylosis

Start date: December 11, 2018
Phase: N/A
Study type: Interventional

Cervical spondylosis is a chronic degenerative condition, commonly affecting >40-year-old adults worldwide. Cervical spondylosis is an important cause of neck pain and low back pain, and seriously affects the physical health, mental health, patients quality of life. Yoga has been most commonly used intervention for pain conditions. But its efficacy in cervical spondylosis has not yet been studied in clinical trials. The primary aim of the present study was to assess the efficacy of yoga chikitsa (therapy) compared with control intervention for neck pain caused by cervical spondylosis.

NCT ID: NCT04039581 Completed - Pain Clinical Trials

KT® in Patients With Cervical Spine Surgery

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

Aim of the study was to investigate the effect of Kinesio taping application on upper trapezius muscle after cervical spine surgery.

NCT ID: NCT03526965 Completed - Clinical trials for Cervical Spondylosis

Yoga Chikitsa for Neck Pain Caused by Cervical Spondylosis

Start date: April 15, 2017
Phase: N/A
Study type: Interventional

Neck Pain caused by Cervical spondylosis (CS) is one of the most common health complaints. Despite its frequency as clinical problem worldwide, there are few evidence-based studies that document efficacy of therapies for neck pain. The aim of this study was to evaluate the effects of Yoga chikitsa (Yoga therapy) on pain and quality of life (QOL) in CS patients compared to usual care.

NCT ID: NCT03425682 Completed - Clinical trials for Degenerative Disc Disease

ViBone in Cervical and Lumbar Spine Fusion

Start date: May 14, 2018
Phase:
Study type: Observational

Assess clinical and radiographic outcomes in patients who undergo 1-3 level anterior cervical discectomy fusion (ACDF) or lumbar interbody fusion (TLIF, PLIF, ALIF, or LLIF) using ViBone.

NCT ID: NCT03364816 Not yet recruiting - Clinical trials for Cervical Spondylosis

Evaluation on Efficacy of Total Artificial Disc Replacement (TDR) of Cervical Spondylosis

Start date: February 1, 2018
Phase: N/A
Study type: Observational

To evaluate the efficacy of 3 different types of cervical disc prosthesis (Prodisc-C, Mobi-C and Prestige-LP) in the treatment of cervical spondylosis.

NCT ID: NCT03358225 Not yet recruiting - Clinical trials for Cervical Spondylosis

A Muti-Center Study Comparing 3 Procedures for Bi-level Cervical Spondylosis

Start date: January 1, 2018
Phase: N/A
Study type: Observational

A muti-center study to compare the safety and efficacy of anterior cervical discectomy and fusion, cervical artificial disc replacement and hybrid surgery for bi-level cervical spondylosis.