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Anti-TNF Therapy and Nerve Conduction Studies in Ankylosing Spondylitis

I

Istanbul Physical Medicine Rehabilitation Training and Research Hospital

Status

Completed

Conditions

Anti - TNF Therapy
Neuropathy
Ankylosing Spondylitis

Treatments

Drug: Anti-TNF agents
Drug: Conventional therapy users for the last 5 years

Study type

Observational

Funder types

Other

Identifiers

NCT04943237
IstPMRTRHatncsias

Details and patient eligibility

About

Patients with ankylosing spondylitis were divided into 2 groups as anti-TNF and conventional therapy according to the treatments they were using for the last 5 years. Nerve conduction studies in the upper and lower extremities of the patients were compared.

Full description

Demyelinating lesions in central nervous system after anti-TNF agents were reported previously. There are limited studies investigating the effects of anti-TNF treatments on the peripheral nervous system. The aim of this study is to investigate whether peripheral nerves are affected due to long-term use of anti-TNF agents.

Patients with a diagnosis of ankylosing spondylitis who received conventional or anti-TNF therapy for five years at Istanbul Physical Therapy and Rehabilitation Training and Research Hospital were included in the study. The patients were divided into two groups as conventional group and anti-TNF group according to the treatment they received. All patients were evaluated in a single section. Sociodemographic characteristics of the patients and Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), Bath Ankylosing Spondylitis Functionality Index (BASFI) and Bath Ankylosing Spondylitis Metrology Index (BASMI) scores were recorded. Median-ulnar motor and sensory conduction studies and tibial-peroneal motor and sural nerve sensory conduction studies were performed in both upper extremities of all patients. Median, ulnar, and tibial nerve F-response studies were also performed.

Enrollment

60 patients

Sex

All

Ages

20 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients diagnosed with ankylosing spondylitis
  • Patients who have been using conventional therapy (non-steroidal anti-inflammatory drugs and/or salazopyrin) or anti-TNF therapy for more than 5 years.

Exclusion criteria

  • Patients with rheumatic diseases (rheumatoid arthritis, systemic lupus erythematosus ......)
  • Patients with other systemic diseases that can lead to neuropathy
  • Patients who have had a known neuropathy or have taken medication that can lead to neuropathy as a side effect
  • Patients with pacemakers

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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