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Clinical Trials/NCT01361542
NCT01361542
Completed
Not Applicable

Effect Of Anti TNF Alpha Therapy On Disease Activity And Bone Health, And Their Adverse Effects In Ankylosing Spondylitis In A North Indian Population

All India Institute of Medical Sciences, New Delhi1 site in 1 country24 target enrollmentFebruary 2011

Overview

Phase
Not Applicable
Intervention
anti TNF alpha agent
Conditions
Ankylosing Spondylitis
Sponsor
All India Institute of Medical Sciences, New Delhi
Enrollment
24
Locations
1
Primary Endpoint
Increase in bone mineral density and decrease in disease activity
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

Ankylosing Spondylitis (AS) is a chronic painful progressive inflammatory arthritis of unknown etiology primarily affecting the spine and sacroiliac joints. In addition to formation of new bone leading to syndesmophytes and ankylosis; osteoporosis is also a prominent feature in AS-thus showing the paradox of new bone formation at abnormal sites coexisting with reduced bone mass & increased fracture risk. Osteoporosis is a common complication of AS, with an incidence between 18.7% and 62%. TNF alpha has a central role in disturbing this balance in bone metabolism--resulting in accelerated alveolar bone loss and decreased strength- i.e. osteoporosis. The investigators hypothesis that anti TNF therapy is effective in active AS resistant to conventional therapy and helps in improving the bone density and over all bone health.

Detailed Description

Ankylosing spondylitis not responding to conventional therapy has been effectively treated with Anti TNF therapy. In addition studies have shown that TNF has a role in osteoporosis of inflammatory diseases. The hypothesis that anti TNF therapy may decrease osteoporosis and tilt bone metabolism to the osteoblastic side has been tested in few studies. These have not been studied in an Indian population. Another great issue in the usage of anti TNF therapy in Indian population is the high incidence of developing infective complications; especially tuberculosis. The investigators are thus studying these in a north Indian population at a tertiary centre. The results would come to important conclusions regarding treatment and in the important issue of tuberculosis screening and prevention.

Registry
clinicaltrials.gov
Start Date
February 2011
End Date
January 2012
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
All India Institute of Medical Sciences, New Delhi
Responsible Party
Principal Investigator
Principal Investigator

S.K.SHARMA

Professor and Head

All India Institute of Medical Sciences, New Delhi

Eligibility Criteria

Inclusion Criteria

  • Patients who are fulfilling the Modified New York Criteria(1984) for the diagnosis of Ankylosing Spondylitis
  • Age ≥ 18 years
  • Patients who have been planned to be started on anti Tnf alpha agents.
  • Patients who have given consent for the study.

Exclusion Criteria

  • Patients with other coexistent rheumatologic diseases.
  • Patients who have previously received anti TNF alpha agents in the past 1 year.
  • Patients who are receiving other medications that may significantly alter the bone metabolism (like steroids, bisphosphonates, estrogen replacement therapy etc)
  • Patients with any contraindications against the usage of anti TNF alpha agents (Active/ chronic infections, liver dysfunction, demyelinating diseases, pregnancy etc)
  • Patients with other definite risk factors for osteoporosis like chronic alcoholism, smoking, endocrine disorders etc

Arms & Interventions

Anti TNF

Anti TNF alpha therapy including either infliximab or etanercept with data obtained before and after the study duration.

Intervention: anti TNF alpha agent

Anti TNF

Anti TNF alpha therapy including either infliximab or etanercept with data obtained before and after the study duration.

Intervention: Anti TNF alpha therapy

Outcomes

Primary Outcomes

Increase in bone mineral density and decrease in disease activity

Time Frame: 2 years

Secondary Outcomes

  • Observation of adverse effects of Anti TNF therapy(2 years)

Study Sites (1)

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