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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT00533650 Completed - Clinical trials for Post-Menopausal Osteoporosis

Proof of Concept (Bone Resorption/Bone Mineral Density) Study (0429-005)

Start date: December 2000
Phase: Phase 2
Study type: Interventional

A study to asses the safety and efficacy of MK0429 in postmenopausal women with osteoporosis.

NCT ID: NCT00532545 Completed - Clinical trials for Osteoporosis, Post-Menopausal

Bone Marker Changes With Teriparatide/Postmenopausal Osteoporosis

Start date: April 2003
Phase: Phase 4
Study type: Interventional

To test the hypothesis that Teriparatide injections given 20 micrograms/daily subcutaneously, for one month, are able to produce reliable changes in the bone marker in a severe osteoporotic population

NCT ID: NCT00532428 Completed - Clinical trials for Osteoporosis, Post-Menopausal

Long Term Effects of Raloxifene Treatment on Bone Quality

Start date: April 2003
Phase: Phase 4
Study type: Interventional

This is a cross-sectional study to determine, via iliac crest bone biopsies, the effect of long-term treatment with raloxifene on histomorphometry and bone quality in patients who participated in the Continuing Outcomes Relevant to Evista Study.

NCT ID: NCT00532337 Completed - Osteoporosis Clinical Trials

Controlled Study of ONO-5334 in Postmenopausal Women With Osteopenia or Osteoporosis

Start date: October 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of ONO-5334 in postmenopausal women with osteopenia or osteoporosis.

NCT ID: NCT00532207 Completed - Clinical trials for Osteoporosis, Post-Menopausal

Study of Teriparatide in the Treatment of Postmenopausal Women With Osteoporosis

Start date: November 2003
Phase: Phase 3
Study type: Interventional

To see if using teriparatide for 12 months will increase Bone Mineral Density at the lumbar spine in postmenopausal women with osteoporosis

NCT ID: NCT00532077 Completed - Osteoporosis Clinical Trials

A Study to Evaluate the Effects of SB-751689 or rhPTH(1-34) on Excretion of Calcium and Phosphate in Women

Start date: August 2007
Phase: Phase 1
Study type: Interventional

SB-751689 may alter calcium and phosphate handling at the kidney level. This study will examine what happens to calcium and phosphate, and other electrolytes, at the kidney after treatment with SB-751689 for 1 month. Another group of subjects will get another drug called Forteo for 1 month to compare the response of the kidney for calcium and phosphate.

NCT ID: NCT00525798 Completed - Osteoporosis Clinical Trials

A Study to Evaluate Oral Salmon Calcitonin in the Treatment of Osteoporosis in Postmenopausal Women Taking Calcium and Vitamin D

Start date: March 2007
Phase: Phase 3
Study type: Interventional

The purpose of this Phase III study is to evaluate the efficacy and safety of oral salmon calcitonin in the treatment of patients with osteoporosis

NCT ID: NCT00523835 Completed - Diabetes Clinical Trials

Body Composition, Bone Mineral Density, Insulin Sensitivity and Echocardiographic Measurements in Klinefelter Syndrome

Start date: April 2002
Phase: N/A
Study type: Observational

Klinefelter syndrome (KS) is the most common sex-chromosome disorder with a prevalence of one in 660 men and is a frequent cause of hypogonadism and infertility. It is caused by the presence of extra X-chromosomes, the most common karyotype being 47,XXY. The phenotype is variable, but the most constant finding is small hyalinized testes, hypergonadotrophic hypogonadism, infertility, eunuchoid body proportion, increased height and learning disabilities. Klinefelter syndrome has been associated with increased prevalence of diabetes, osteoporosis and cardiovascular diseases but the pathogenesis is unknown. Accordingly the aim of the study was to investigate measures of body composition, insulin sensitivity, bone mineral density, echocardiography, as well as biochemical markers of endocrine, metabolic and bone function in KS and an age-matched control group.

NCT ID: NCT00523341 Completed - Osteoporosis Clinical Trials

Extension Study to Evaluate the Long Term Safety and Efficacy of Denosumab in the Treatment of Osteoporosis

Start date: August 7, 2007
Phase: Phase 3
Study type: Interventional

The primary objective was to describe the safety and tolerability of up to 10 years or 7 years denosumab administration as measured by adverse event monitoring, immunogenicity and safety laboratory parameters in participants who previously received denosumab or placebo, respectively.

NCT ID: NCT00520052 Completed - Osteoporosis Clinical Trials

Frequency of Zoledronic Acid to Prevent Further Bone Loss in Osteoporotic Patients Requiring Androgen Deprivation Therapy for Prostate Cancer

Start date: August 2003
Phase: N/A
Study type: Interventional

The aim of this study is to determine if 3 monthly infusions of zoledronic acid, given over one year, improves the bone mineral density in osteoporotic patients undergoing androgen deprivation therapy for prostate cancer