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Clinical Trials/NCT04943237
NCT04943237
Completed
Not Applicable

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

Istanbul Physical Medicine Rehabilitation Training and Research Hospital1 site in 1 country60 target enrollmentJuly 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anti - TNF Therapy
Sponsor
Istanbul Physical Medicine Rehabilitation Training and Research Hospital
Enrollment
60
Locations
1
Primary Endpoint
nerve conduction studies
Status
Completed
Last Updated
4 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
July 1, 2019
End Date
October 1, 2019
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Istanbul Physical Medicine Rehabilitation Training and Research Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

nerve conduction studies

Time Frame: All patients were evaluated in one session. The assesment of a patient lasted nearly 45-60 minutes

The evaluation of median, ulnar, tibial, peroneal and sural nerves

Study Sites (1)

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