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ordosis, Disc Herniation and Cervical Radiculopathy

Not Applicable
Conditions
Musculoskeletal Diseases
Registration Number
PACTR201604001574574
Lead Sponsor
Ibrahim Moustafa Moustafa
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Subjects were included if
the AHT distance was more than 15.
their ARA was less than 25° .
they had a unilateral C7 discogenic radiculopthy .
C7 dermatomal numbness.
current continuous or intermittent pain or discomfort which had persisted for more than 3 months.
radiation of arm pain in the representative dermatomal areas for C7.
diminished deep tendon reflexes in the affected arm.
the four positive examination findings (Spurling test, upper limb tension test, cervical distraction test, and less than 60° cervical rotation towards the symptomatic side).
side to side amplitude differences of 50% or more in dermatomal somatosensory evoked potentials.
duration of symptoms more than 3 months.

Exclusion Criteria

Exclusion criteria included
the presence of any signs or symptoms of medical red flags (e.g., tumor, fracture, rheumatoid arthritis, osteoporosis, and prolonged steroid use).
A history of previous cervical or thoracic spine surgery.
signs or symptoms of upper motor neuron disease.
vestibulobasilar insufficiency. amyotrophic lateral sclerosis.
bilateral upper extremity radicular symptoms.
pregnant woman.
inability to tolerate cervical flexion or extension position.
the complete loss of sensation along the involved nerve root.
intractable pain.
myelopathy.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
disability measured using the valid and reliable neck disability index
Secondary Outcome Measures
NameTimeMethod
cervical sagittal alignment, and the neurophysiological findings (latency and peak-to-peak amplitude of DSSEPs) in addition to central somatosensory evoked potential N13-N20.
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