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Comparison of the therapeutic effect of limaprost and pregabalin on upper limb sensory neuropathy in patients with cervical radiculopathy, among patients with acquired lumbar spinal stenosis.

Comparison of the therapeutic effect of limaprost and pregabalin on upper limb sensory neuropathy in patients with cervical radiculopathy, among patients with acquired lumbar spinal stenosis.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0008042
Enrollment
80
Registered
2022-12-29
Start date
2023-02-01
Completion date
Unknown
Last updated
2023-01-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Kyung Hee University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Patients with cervical radiculopathy among patients with acquired lumbar spinal stenosis who visited our hospital - Patients with recorded upper extremity sensory nerve abnormalities (numbness, hypoesthesia) (NRS), upper extremity pain (NRS), neck pain (NRS), NDI, JOA score (sensory section), EQ-5D, subjective satisfactory rate (Odom's criteria) - Adults over 20 years of age who can express his/her pain or functional abnormalities.

Exclusion criteria

Exclusion criteria: - Among patients with acquired lumbar spinal stenosis, patients with cervical radiculopathy who have previously undergone surgical treatment in the cervical region - Among patients with acquired lumbar spinal stenosis, in addition to cervical radiculopathy, patients with other underlying diseases that may affect the outcome evaluation by causing upper limb sensory nerve abnormalities. ex) Carpal tunnel syndrome, cubital tunnel syndrome, Parkinson disease - Adolescents under the age of 20 or pregnant women - Patients who are medically incapable of consent or unable to communicate - Patients with bleeding tendency due to history and medications taken - Patients with lactose intolerance

Design outcomes

Primary

MeasureTime frame
Pain(Numeral rating scale)

Secondary

MeasureTime frame
Numbness(Numeral rating scale) ;NDI(Neck disability index) score;Japanese Orthopaedic Association (JOA) score;EQ-5D(Health Related Quality of Life);subjective satisfactory rate(Odom’s criteria)

Countries

Korea, Republic of

Contacts

Public ContactKyung Chung Kang

Kyung Hee University

futurespine@gmail.com+82-2-958-8348

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026