Actively Recruiting

Phase Not Applicable
Age: 20Years - 60Years
All Genders
NCT06653543

Effect of Mulligan on Cervical Radiculopathy

Led by Cairo University · Updated on 2025-04-27

40

Participants Needed

1

Research Sites

31 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to investigate the effect of Mulligan mobilization with arm movement on nerve conduction velocity in patients with unilateral cervical radiculopathy. The main questions it aims to answer are : 1. Is there a statistical significant effect of mobilization with arm movement on NCV velocity in treatment of cervical radiculopathy ? 2. Is there a statistical significant effect of mobilization with arm movement on pain level in treatment of cervical radiculopathy ? 3. Is there a statistical significant effect of mobilization with arm movement on cervical ROM in treatment of cervical radiculopathy ? 4. Is there a statistical significant effect of mobilization with arm movement on neck disability level in treatment of cervical radiculopathy ? The course of treatment involves 6 sessions over the course of 3 weeks participants will be divided into 2 groups : Control group : recieves only Conventional treatment Experimental group : recieves Conventional treatment and Mulligan mobilization with arm movement .

CONDITIONS

Official Title

Effect of Mulligan on Cervical Radiculopathy

Who Can Participate

Age: 20Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with cervical radiculopathy
  • Aged between 20 and 60 years
  • Unilateral radiating pain along the median nerve
  • Positive upper limb tension test (ULTT 1)
  • Male or female gender
  • Able to understand instructions and willing to participate
Not Eligible

You will not qualify if you...

  • History of trauma, dislocation, or subluxation of the upper extremity
  • Rheumatoid arthritis
  • Malignancy
  • Spinal canal stenosis
  • Cervical instability or spondylolisthesis
  • Vertebral-basilar insufficiency (VBI)
  • Referred pain from cardiac ischemia
  • Previous cervical or thoracic spine surgeries
  • Systemic causes like diabetic neuropathy
  • Recent fracture or surgery around the shoulder
  • Carpal tunnel syndrome
  • Thoracic outlet syndrome

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Kafr El-Sheikh university

Kafr El-Sheikh Governorate, Kafr el-Sheikh Governorate, Egypt, 33516

Actively Recruiting

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Research Team

E

Elgazar

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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