跳至主要内容
临床试验/EUCTR2005-005399-34-BE
EUCTR2005-005399-34-BE进行中(未招募)不适用

A randomised, open-label, multi-national study to investigate the impact of bone marker feedback (at 2 months) on adherence to once monthly Ibandronate treatment for post-menopausal osteoporosis (PMO) - BEATRIS

.V. Roche S.A.0 个研究点目标入组 800 人开始时间: 2006年1月9日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
800

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • - Ambulatory post-menopausal women aged 55-85 years eligible for bisphosphonate treatment or with documented osteoporosis as determined by the treating physician in accordance with local practice;
  • - Patients who are either naïve to bisphosphonates or lapsed bisphosphonate users (last bisphosphonate intake > 6 months ago);
  • - Patients who, in the opinion of the investigator, are able to understand and complete the questionnaires, are willing and able to comply with the protocol requirements;
  • - Patients who have signed the informed consent.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Hypersensitivity to bisphosphonates;
  • - Inability to stand or sit in an upright position for at least 60 minutes;
  • - Inability to swallow a tablet whole;
  • - Contraindications to calcium or vitamin D therapy;
  • - Administration of any investigational drug within 30 days preceding the first dose of the study drug;
  • - Uncorrected hypocalcemia or other disturbances of bone and mineral metabolism;
  • - Administration of antiresorptive medication within the last 6 months (bisphosphonates, SERMs, calcitonin and hormone replacement therapy);
  • - Active disease/ disorder known to influence bone metabolism; eg. liver disease, chronic alcoholism, severe malabsorption syndrome, documented active thyroid disease without treatment;
  • - Renal impairment (creatinine clearance <30 mL/min);
  • - History of major upper GI disease defined by:
  • - Significant upper GI bleeding within the last year requiring hospitalization or
  • transfusion;
  • - Recurrent peptic ulcer disease documented by radiographic or endoscopic means;
  • - Dyspepsia or gastroesophageal reflux that is uncontrolled by medication;
  • - Abnormalities of the esophagus that delay esophageal emptying, such as
  • stricture, achalasia , or dysmotility;
  • - Active gastric/duodenal ulcers.

研究者

发起方
.V. Roche S.A.

相似试验

进行中(未招募)
1 期
A randomised, open-label, multi-national study to investigate the impact of bone marker feedback (at 2 months) on adherence to once monthly Ibandronate treatment for post-menopausal osteoporosis (PMO) - BEATRISosteoporosis in postmenopausal women
EUCTR2005-005399-34-IE.V. Roche S.A.800
进行中(未招募)
不适用
A randomised, open-label, multi-national study to investigate the impact of bone marker feedback (at 2 months) on adherence to once monthly Ibandronate treatment for post-menopausal osteoporosis (PMO) - BEATRISosteoporosis in postmenopausal women
EUCTR2005-005399-34-AT.V. Roche S.A.800
进行中(未招募)
不适用
A randomised, open-label, multi-national study to investigate the impact of bone marker feedback (at 2 months) on adherence to once monthly Ibandronate treatment for post-menopausal osteoporosis (PMO) - BEATRISosteoporosis in postmenopausal women
EUCTR2005-005399-34-GR.V. Roche S.A.580
进行中(未招募)
不适用
A randomised, open-label, multi-national study to investigate the impact of bone marker feedback (at 2 months) on adherence to once monthly Ibandronate treatment for post-menopausal osteoporosis (PMO) - BEATRIS
EUCTR2005-005399-34-PT.V. Roche S.A.800
进行中(未招募)
不适用
Study to prevent major vascular events with Ticagrelor compared to Aspirin in patients with Acute Ischaemic Stroke or TIAischaemic strokeMedDRA version: 18.1Level: LLTClassification code 10055221Term: Ischemic strokeSystem Organ Class: 100000004852
EUCTR2012-003895-38-SKAstraZeneca AB13,600