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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT02194647 Active, not recruiting - Osteoporosis Clinical Trials

Anti-osteoporosis Medication Monitoring and Management Service

Start date: July 2014
Phase:
Study type: Observational

BACKGROUND: One-year adherence to oral anti-osteoporosis medication (AOMs) was only about 30%. In recent years, efforts have been made to change the delivery of these medications from oral form to injection form every, 3, 6 or 12 months to increase adherence. However, both patients and providers are sometimes confused about the multiple choices. Also, patients may receive extra medications if providers did not keep tract of their previous AOM uses or patients may changes providers. There were urgent needs to provide AOM monitoring and management services to improve cares. OBJECTIVES: To establish a anti-osteoporosis medication management service at National Taiwan University Hospital and its BeiHu Branch. METHODS: Participating physicians will select those eligible for services and refer to study coordinators. Study coordinators will conduct baseline assessments on osteoporosis/fracture risks, record medical conditions, AOMs, provide educations on osteoporosis, fracture, sarcopenia, fall, medications, nutrition, and exercise. They also arrange return clinic visit, telephone reminder and follow up for patients, and communicate with providers on regular bases. the investigators plan to enroll 500 patients with 18-month follow up for each.

NCT ID: NCT02186171 Completed - Osteoporosis in Men Clinical Trials

A Study to Compare the Safety and Efficacy of Romosozumab (AMG 785) Versus Placebo in Men With Osteoporosis

BRIDGE
Start date: June 16, 2014
Phase: Phase 3
Study type: Interventional

The study is designed to evaluate if treatment with romosozumab once a month for 12 months compared with placebo is effective in increasing bone mineral density (BMD) at the lumbar spine. Additionally, the study will assess the effect of treatment with romosozumab for 12 months compared with placebo on BMD at the femoral neck and total hip.

NCT ID: NCT02184962 Completed - Osteoporosis Clinical Trials

Periodontal Disease and Post-menopausal Osteoporosis

Start date: May 2012
Phase: N/A
Study type: Observational

The aim of this study was to investigate the levels of RANKL and Osteoprotegerin, and their relationship in gingival crevicular fluid of post-menopausal women with osteoporosis/osteopenia and chronic periodontitis simultaneously and evaluate the effect that the use of bisphosphonates in periodontal disease. Study hypothesis: "The osteoporosis / osteopenia in postmenopausal women patients with periodontal disease affect the ratio RANKL / OPG in gingival crevicular fluid samples favoring osteoclastogenesis processes "

NCT ID: NCT02176382 Completed - Clinical trials for Postmenopausal Osteoporosis

Denosumab and Teriparatide Study (DATA-HD and DATA-EX)

DATA-HD
Start date: August 2014
Phase: Phase 4
Study type: Interventional

The aim of the study is to assess the effect of an antiresorptive medication in combination with standard dose or alternate dose teriparatide. The study extension will evaluate the effect of one-dose of zoledronic acid after the teriparatide/denosumab combination.

NCT ID: NCT02174666 Completed - Osteoporosis Clinical Trials

Isoflavone Treatment for Postmenopausal Osteopenia.

Start date: June 2014
Phase: N/A
Study type: Interventional

The aim of the project is to execute a double-blind, parallel, randomized 12-month intervention trial on postmenopausal women with osteopenia (low bone mineral density), in order to determine the effects of daily intake of fermented red clover (RC) extract on estrogen dependent bone mineral resorption when compared to placebo. Both groups will recieve equivalent daily calcium, vitamin D and magnesium supplements. The project will also assess whether bioactive compounds in RC can reduce the risk of developing cardiovascular disease.

NCT ID: NCT02166437 Recruiting - Osteoporosis Clinical Trials

Clinical Results of Bisphosphonate and Denosumab Therapy Following Teriparatide Therapy for Japanese

Start date: November 2013
Phase: N/A
Study type: Observational

In this study, the investigators would like to analyze the bone mineral density (BMD) , bone turnover makers, and fracture prevention effects of bisphosphonate and denosumab randomly divided following daily teriparatide in Japanese patients under clinical practice. The participants are treated in the investigators hospital, who are under severe osteoporotic condition.

NCT ID: NCT02165527 Completed - Osteoporosis Clinical Trials

Evaluation of Bone Length Measurement

Start date: November 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if Lunar iXDA scanning with the use of a computer software program can make accurate measurements of the length of leg bones compared to conventional x-rays.

NCT ID: NCT02163668 Completed - Osteoporosis Clinical Trials

Effects of Yoga on Bone Metabolism in Premenopausal Women

Start date: September 2009
Phase: N/A
Study type: Interventional

This study examined the effects of 8 months of Yoga training on bone density and bone turnover markers in premenopausal women, ages 35-50 years. The style of Yoga used was power Yoga that involved postures with a jumping component. The investigators hypothesized that the Yoga intervention would result in beneficial improvements in bone turnover markers, by increasing the bone formation marker and decreasing the bone resorption marker.

NCT ID: NCT02162277 Completed - Osteoporosis Clinical Trials

Therapeutic Strategy in Postmenopausal Women Using Osteoporotic Diagnostic Kits

Start date: January 2013
Phase:
Study type: Observational

The frequency of osteoporosis in Japan is increasing. Also, the frequency of osteoporosis-based fractures in postmenopausal women is increasing. Therefore, it is urgently required to improve osteoporosis. Life expectancy in Nagano prefecture is the longest in Japan, however, healthy life expectancy in Nagano is not very long in Japan. There are several problems in this issue from the medical site and the patient site. The aim of this study is, from the patient site, to increase the motivation of postmenopausal women for osteoporosis using osteoporotic diagnostic kit.

NCT ID: NCT02157948 Completed - Clinical trials for Postmenopausal Osteoporosis

A Double-blind Study to Assess the Efficacy and Safety of Denosumab Produced by Two Different Processes in Postmenopausal Women With Osteoporosis

Start date: May 2014
Phase: Phase 3
Study type: Interventional

This study will compare the effect of denosumab produced by two different manufacturing processes on bone mineral density at the lumbar spine in postmenopausal women with osteoporosis.