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Clinical Trials/NCT05145530
NCT05145530
Completed
Phase 2

Selective Nerve Root Block With Ultrasound Guidance Improves Surgical Outcome of Selective Discectomy in Patients With Multilevel Cervical Disc Disease: a Randomized Controlled Trial

Assiut University1 site in 1 country60 target enrollmentAugust 10, 2017

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Selective Nerve Root Block
Sponsor
Assiut University
Enrollment
60
Locations
1
Primary Endpoint
pain intensity
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Disc degeneration is a natural part of growing older. Up to 60% of asymptomatic people have MRI findings that are positive. As a result, MRI only provides morphological information and may not be able to determine the clinical significance of the findings.

Detailed Description

Many authors believe that patients who suffer from cervical radiculopathy as a result of degenerative disease and have multilevel pathology on imaging studies still have moderate surgical outcomes. This occurs due to a misdiagnosis or the need to perform surgery on multiple levels despite a single painful lesion. Although the complication rate for 1- and 2-level ACDF is so low that it is considered one of the safest procedures in spine surgery. There is concern that increasing levels of fusion will lead to more complications, such as a higher incidence of persistent axial neck pain, dysphagia, and vertebral artery injury, as well as more postoperative pain and higher narcotic dosages.

Registry
clinicaltrials.gov
Start Date
August 10, 2017
End Date
April 30, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ghada Mohammed AboelFadl

Principal investigator

Assiut University

Eligibility Criteria

Inclusion Criteria

  • all patients presented with unilateral brachialgia due to multilevel cervical disc disease

Exclusion Criteria

  • multilevel cervical disc disease who had bilateral brachialgia,
  • myelopathy, double crush syndrome,
  • ossified posterior longitudinal ligament (OPLL),
  • combined anterior and posterior pathology requiring posterior decompression

Outcomes

Primary Outcomes

pain intensity

Time Frame: 24 hours postoperative

Visual analogue score (VAS): 0= no pain, 10= worst pain

Study Sites (1)

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