Assessment of Peripheral Neuropathy in Ankylosing Spondylitis

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssiut University

About this trial

investigators hypothesized that peripheral neuropathy in ankylosing spondylitis is associated with higher disease activity, greater central sensitization, worse functional impairment, and poorer quality of life.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients aged ≥18 years

Diagnosis of ankylosing spondylitis according to the modified New York criteria (6).

Ability to provide informed consent

Disqualifiers

Patients under the age of 18 years.

Patients with definite diagnosis for any other systemic autoimmune disorders.

Diabetes mellitus

Chronic renal or hepatic disease

Trial population

Patients aged ≥18 years with Diagnosis of ankylosing spondylitis according to the modified New York criteria

Trial design

Design model

Case-only

Time perspective

Cross-sectional

Treatments tested in this trial

  • Nerve conduction study

    Diagnostic test

    Peripheral neuropathy will be evaluated using nerve conduction studies (NCS) for upper and lower limbs peripheral nerves performed according to standard electrophysiological techniques.

Treatment groups

45 Participants
are divided into 1 treatment group
Group A: Ankylosing spondylitis Patients1 intervention

Trial outcomes

Primary outcomes

1

presence of peripheral neuropathy

Peripheral neuropathy will be evaluated using nerve conduction studies (NCS) for upper and lower limbs peripheral nerves performed according to standard electrophysiological techniques.

Time frame
1 month

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: