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Anti-TNF Therapy and Nerve Conduction Studies in Ankylosing Spondylitis

Anti-TNF Therapy and Nerve Conduction Studies in Patients With Ankylosing Spondylitis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04943237
Enrollment
60
Registered
2021-06-29
Start date
2019-07-01
Completion date
2019-10-01
Last updated
2021-06-29

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

Conditions

Anti - TNF Therapy, Ankylosing Spondylitis, Neuropathy

Brief summary

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.

Detailed 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.

Interventions

Group of patients using anti-TNF for the last 5 years.

DRUGConventional therapy users for the last 5 years

Group of patients not using anti-TNF. Group of patients using conventional therapy (non -steroid anti-inflammatory drugs and/or salazopyrin) for the last 5 years

Sponsors

Istanbul Physical Medicine Rehabilitation Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
nerve conduction studiesAll patients were evaluated in one session. The assesment of a patient lasted nearly 45-60 minutesThe evaluation of median, ulnar, tibial, peroneal and sural nerves

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026