A 2-year Observational Study of Bone Density and Bone Turnover After Prior Treatment With Alendronate, Ibandronate and Risedronate for Postmenopausal Osteoporosis in Secondary Care
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 86
- 试验地点
- 1
研究概览
简要总结
This is a 2year observational study that will recruit patients who have previously completed a randomised, open label, parallel, single centre study (TRIO Study) of three bisphosphonates: alendronate, ibandronate and risedronate. These drugs are the most commonly used group of treatments for postmenopausal osteoporosis in the UK. However, the length of time for which these treatments continue to work after they are stopped has not been fully elucidated. Without this information it is unclear as to how long doctors should treat and whether it would be good practice to give drug 'holidays'.
The investigators plan to compare the effects on bone quantity and quality of stopping these licensed bisphosphonates in patients who have taken the medication for a duration of two years. The investigators aim to recruit up to 100 postmenopausal and up to 100 premenopausal (reference range) subjects. Measurements collected at the final visit of the previous study will be used for 'baseline' values for this study.
The postmenopausal group will have an initial study visit to secure informed consent, and then further study visits at 24, 48, 72 and 96 weeks after stopping medication. Visit procedures will include:
Blood and urine samples for measurements of bone biomarkers Bone Mineral Density of the spine, hip, whole body, forearm Dual-emission X-ray absorptiometry (DXA), and heel dual X-ray and Laser (DXL) Quantitative Ultrasound of Bone (QUS) Vertebral Fracture Assessment (VFA).
The premenopausal group will have one study visit, 96 weeks after completing the previous study. Visit procedures will include:
Blood and urine samples for measurements of bone biomarkers Bone Mineral Density of the spine and hip (DXA)
A subgroup of 50 premenopausal women will also have the following measurements:
Bone Mineral Density of the whole body, forearm (DXA), and heel (DXL) Quantitative Ultrasound of Bone (QUS).
详细描述
The current study is an observational study aiming to compare the effects of stopping medication on bone quantity and quality, in patients who have previously taken bisphosphonate drugs for a duration of two years.
This study will recruit participants who have previously completed the TRIO study. The TRIO study aimed to compare the effects of three licensed bisphosphonates on bone quantity and quality. Participants in the treatment group of the TRIO study were randomised to treatment with one of three licensed bisphosphonates (alendronate, ibandronate and risedronate) for a duration of two years.
Measurements taken at the final TRIO study visit will be used as 'baseline' values for this study. The postmenopausal group will have an informed consent visit, followed by further study visits at 24, 48, 72 and 96 weeks after stopping medication.
Study visit procedures for the postmenopausal group will include:
Blood and urine samples for measurements of bone biomarkers at 24, 48, 72 and 96 weeks off treatment.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- — 至 87 Years（Child, Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Inclusion Criteria for postmenopausal women
- •female be at least 7 years postmenopausal but less than 87 years of age
- •be ambulatory
- •be able and willing to participate in the study and provide written informed consent.
- •have taken a bisphosphonate for 2 years as a participant in the TRIO study and be compliant > 80%
- •have a Bone Mineral Density (BMD) T score > -2.5 at the femoral neck
- •Inclusion Criteria for premenopausal women
- •be able and willing to participate in the study and provide written informed consent
- •have previously taken part as premenopausal controls in the TRIO study
- •be in good general health as determined by past medical and physical history
- •be bisphosphonate naive; premenopausal women.
排除标准
- •Exclusion Criteria for postmenopausal women:
- •An incident vertebral fracture or more than 5%/year bone loss at the spine or hip during the 2-year TRIO study
- •Evidence of a clinically significant organic disease which could prevent the patient from completing the study, including diabetes
- •Abuse of alcohol or use of illicit drugs or who consumed more than 4 units of any alcoholic beverage one day prior to the visit (i.e. subjects who might be binge drinkers)
- •A history of cancer within the past 5 years excluding skin cancer non melanomas
- •A history of ongoing conditions or diseases known to cause abnormalities of calcium metabolism or skeletal health (secondary osteoporosis)
- •Chronic renal disease (as defined by a creatinine clearance of ≤ 30ml/min)
- •Acute or chronic hepatic disease
- •Malabsorption syndromes
- •Hyperthyroidism as manifested by Thyrotrophin-stimulating hormone (TSH) outside the lower limit of the normal range
- •Hyperparathyroidism
- •Hypocalcemia or hypercalcemia
- •Osteomalacia
- •Cushing's syndrome
- •Current use of glucocorticoid therapy
- •A serum calcium less than 2.2 mmol/l and a Parathyroid hormone (PTH) above 75ng/l
- •A history of any known condition that would interfere with the assessment of Dual-emission X-ray absorptiometry (DXA) at either lumbar spine or femoral neck
- •Markedly abnormal clinical laboratory parameters that are assessed as clinically significant by the principal investigator
- •Require, in the opinion of the consulting physician, continuation of bisphosphonate therapy.
- •Exclusion Criteria for premenopausal women:
- •Are pregnant or nursing (lactating)
- •Use of any hormonal forms of contraception/ therapy within the past 2 years that would, in the opinion of the consulting physician, affect bone metabolism.
- •Use of anabolic agents such as steroids or PTH, or any bisphosphonate within the past 2 years.
- •Have any history of cancer within the past 5 years. Relatively benign skin malignancies, such as basal cell carcinoma or squamous cell carcinoma, are not an exclusion if the patient has been in remission for at least 6 months prior to enrolment.
- •Have any chronic disease (HIV or AIDs, clinically significant renal or cardiovascular disease, hyperthyroidism, diabetes, hyperlipidemia) or menstrual cycle irregularity (by history)).
- •Have any metabolic bone disease, such as osteoporosis, Paget 's disease, osteogenesis imperfecta, or serious illness affecting normal bone homeostasis (by history and physical exam if required)
- •Significant use of any medications known to affect bone metabolism (such as Phenytoin or other anticonvulsants, Selective Estrogen Receptor Modulators (SERMs), heparin or systemic glucocorticosteroids) within the past 2 years.
- •Have suffered a fracture within the last 12 months
- •Have anorexia nervosa, suspected bulimia (by history or physical) or obvious malnutrition
- •Have a history of alcoholism, or who have consumed more than 4 units of any alcoholic beverage one day prior to the visit (i.e., subjects who might be binge drinkers)
- •Have previously participated in active therapy clinical trials within the last 3 months