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Completed

NCT Number: NCT01465568

Denosumab in Current Users of Bisphosphonates for Glucocorticoid-induced Osteoporosis

The purpose of this study is to study the efficacy of denosumab, a new drug, in the treatment of osteoporosis in patients using bisphosphonates.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Tuen Mun Hospital

Hong Kong, China

About this study

There are no data on the use of denosumab in steroid induced osteoporosis. Postmenopausal women with chronic use of Glucocorticoid (GCs) are at high-risk of osteoporotic fractures. Despite bisphosphonate treatment, a certain proportion of high-risk patients using chronic GCs either do not achieve a satisfactory gain in bone mineral density (BMD) or develop new fragility fractures. Thus, more potent osteoporosis treatment is necessary for this subgroup of patients. This prompts the current study which aims to examine the efficacy of denosumab in current users of oral bisphosphonates for Glucocorticoid-induced Osteoporosis (GIOP).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Women or adult men (>18 years of age) with various medical diseases requiring long-term prednisolone treatment. Pre-menopausal women should have no plan for pregnancy within 2 years of study entry and agree to practice contraception during this 2-year period.
  • A daily dose of prednisolone (or equivalent) of more than 2.5mg within 3 months of study entry.
  • Having received oral bisphosphonate treatment for at least 2 years.
  • Suboptimal response to bisphosphonate treatment, defined as either one of the following: (1) failure of lumbar spine, femoral neck or total hip BMD values to increase; (2) values of lumbar spine, femoral neck or total hip BMD remain osteoporotic, ie. T scores < -2.5 or Z scores < -2.0; or (3) development of new fragility vertebral or non-vertebral fractures despite at least 2 years' treatment with good compliance.
  • Informed consent from patients.

Exclusion criteria

  • Patients with previous use of denosumab or teriparatide.
  • Premenopausal women who plan for pregnancy within 2 years of study entry or who do not agree for contraception within this 2-year period.
  • Patients with known bone disorders such as osteomalacia, renal osteodystrophy, and hyperparathyroidism.
  • Patients with unexplained hypocalcemia.
  • Patients with serum creatinine level of >=200umol/L.

Treatment and study plan

Denosumab

Drug

60mg subcutaneous injection 6 monthly for 2 doses

Other names: Prolia

Bisphosphonates

Drug

continue present bisphosphonate treatment

Other names: continuation of bisphosphonates in their usual dosages

Primary outcomes

  1. bone mineral density (BMD) changes at the lumbar spine

    Time frame: baseline, 6 months and 12 months

Secondary outcomes

  1. BMD changes in the total hip and femoral neck

    Time frame: baseline, 6 months and 12 months

  2. bone turnover markers

    Time frame: baseline, 6 months and 12 months

  3. New vertebral fractures

    Time frame: 12 months

  4. adverse events

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

Tuen Mun Hospital

Other Gov

Registry information

Official study title

Denosumab in Current Users of Bisphosphonates for Glucocorticoid-induced Osteoporosis: a Randomized Controlled Trial

Important dates

Study start
2011
Primary completion
2014
Study completion
2014
First posted
Nov 7, 2011
Registry last updated
May 12, 2015

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.

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