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Completed

NCT Number: NCT00941473

Effect of Epidural Steroid Injection on Bone Mineral Density in Postmenopausal Women

To evaluate for the effect of corticosteroid epidural injections on bone mineral density in postmenopausal women. Candidates for the study: Post menopausal women between the ages of 55 and 80. No history of bone disease. No thyroid/parathyroid disorder. not used injected or oral steroids in the last year. No recent smoking.

The purpose is to identify any significant change in bone mineral density with the use of epidural steroid injections. This may implicate the need for patient counseling regarding this possible side effect and the possible use of preventive measures to avoid this adverse effect.

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Key information

Age range

55 year–80 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

Henry Ford Hospital W. Bloomfield

West Bloomfield, Michigan, 48322, United States

About this study

Glucocorticoids reduce bone formation and increase bone loss via a variety of mechanisms. This effect has been shown to be dose-dependent. Doses as low as 10mg of Prednisone, has been shown to lower bone density over periods as short as 20 weeks, an effect which may be prevented with use of Calcium and Vitamin D. Inhaled Tramcinilone has also been shown to lead to dose-related loss of bone at the hip in premenopausal women. Clinic visits will be arranged for recruited patients at baseline and then at 3 and 6 months after the ESI and at any time for new-onset or severe back pain. During the initial visit, consent will be obtained, patient will be given details on the study design and rationale, severity and characteristics of back pain. Epidural corticosteroid injection (ESI) has been shown to decrease pain, speed return of function, and improve neurological signs in patients presenting with low back pain.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients with low back pain and have consented to ESI. Age 55 and 5 years postmenopausal Caucasian women.

Exclusion criteria

  • any women who doesn't meet the inclusion criteria
  • Women with history of a disease affection bone turnover
  • Women taking any drugs known to influence bone metabolism
  • Women who had smoked within the preceding year
  • Women with abnormal serum thyrotropin concentration, or high parathyroid hormone concentratons.
  • Women who had received more than two short courses (lasting 2 weeks or less) of oral or parenteral glucocorticoids in the preceding year or any oral or pareneteral or local (intraarticular, paraspinal,...) or inhaled glucocorticoids in the preceding year
  • Women diagnosed with osteoporosis (T score<=2.5) on baseline DXA or had history of osteoportic fracture.
  • Pregnant women
  • Severe scoliosis -

Treatment and study plan

Triamcinilone (kenalog)

Drug

Epidural steroid injection of 80mg of Triamcinilone.

Primary outcomes

  1. Measurements will be taken at baseline and then repeated at 3,6, and 12 months after treatment.

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

Henry Ford Health System

Other

Registry information

Important dates

Study start
2007
Primary completion
2011
Study completion
2011
First posted
Jul 17, 2009
Registry last updated
Feb 20, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.