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Osteoporosis, Postmenopausal clinical trials

View clinical trials related to Osteoporosis, Postmenopausal.

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NCT ID: NCT00787904 Completed - Osteoporosis Clinical Trials

Role of T-cells in Post-Menopausal Osteoporosis

Start date: December 2006
Phase: N/A
Study type: Observational

This is an observational study of women undergoing surgical menopause to determine whether T-cells play an important role in the etiology of post-menopausal osteoporosis. Subjects will examined before and after surgery and followed over a two year period to determine the biology of T-cells during this study period.

NCT ID: NCT00778154 Completed - Clinical trials for Postmenopausal Osteoporosis

Study of Bone Histomorphometry, Microarchitecture, and Matrix Structure in Patients Receiving Alendronate or Risedronate

Start date: January 2004
Phase: N/A
Study type: Observational

Patients who have received the appropriate number of years of alendronate or risedronate therapy will be recruited. Each patient will have received baseline BMD measurements performed at the spine and the hip by DXA. Each patient will receive tetracycline to label the bone and then have a transiliac bone biopsy. One year later teh bone label and biopsy procedure will be repeated.

NCT ID: NCT00745121 Completed - Osteopenia Clinical Trials

Study Evaluating ASTRA TECH Implant System, OsseoSpeed™ Implants in the Upper Jaw in Women With Osteoporosis

Start date: July 16, 2008
Phase: N/A
Study type: Interventional

The overall objective of the study is to compare treatment with the ASTRA TECH Implant System, OsseoSpeed™ implant in the maxilla of postmenopausal women with and without systemic osteoporosis. The hypothesis is that there will be no difference in marginal bone level alterations between the two groups.

NCT ID: NCT00729651 Completed - Clinical trials for Osteoporosis Postmenopausal

Efficacy and Safety Study of Fosamax Plus D in Postmenopausal Women With Osteoporosis (0217A-263)

Start date: March 20, 2008
Phase: Phase 4
Study type: Interventional

To demonstrate the efficacy/safety of Fosamax Plus D

NCT ID: NCT00718861 Completed - Clinical trials for Post-menopausal Osteoporosis

3 yr Efficacy & Safety Study of Zoledronic Acid in Post-menopausal Women With Osteoporosis Treated With Zol Acid for 6 Yrs

Start date: May 2008
Phase: Phase 3
Study type: Interventional

This second extension will evaluate the efficacy and long term safety of zoledronic acid in women with post-menopausal osteoporosis

NCT ID: NCT00696644 Completed - Osteoporosis Clinical Trials

A Study for Teriparatide in Severe Osteoporosis

ISSO
Start date: June 2008
Phase: N/A
Study type: Observational

This observational study will evaluate the incidence of new vertebral and non vertebral fragility fractures in patients with severe osteoporosis treated with anabolic drugs. This study will also evaluate BMD, compliance to treatment, back pain and the health-related quality of life.

NCT ID: NCT00676312 Completed - Clinical trials for Postmenopausal Osteoporosis

Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Effect of PTH134 at Increasing Doses in Healthy Postmenopausal Subjects

Start date: May 2008
Phase: Phase 1
Study type: Interventional

This study is designed to investigate the safety and tolerability of PTH134 in healthy subjects and to assess the exposure from PTH134.

NCT ID: NCT00674453 Completed - Bone Loss Clinical Trials

The Prevention Of Postmenopausal Osteoporosis With Lasofoxifene And Cytokine Evaluation

LACE
Start date: September 2004
Phase: Phase 2
Study type: Interventional

The objective of the study is to demonstrate the effects that lasofoxifene has on serum markers of bone metabolism.

NCT ID: NCT00670501 Completed - Clinical trials for Osteoporosis, Postmenopausal

Effects of Teriparatide in the Treatment of Postmenopausal Women With Osteoporosis

Start date: August 1996
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to demonstrate a reduction in the proportion of new vertebral fractures in postmenopausal women with osteoporosis following 3-years of treatment with 20 and 40 mcg/day of teriparatide plus calcium and vitamin D compared with calcium and vitamin D alone.

NCT ID: NCT00670319 Completed - Clinical trials for Osteoporosis, Postmenopausal

Comparison of Raloxifene Hydrochloride and Placebo in the Treatment of Postmenopausal Women With Osteoporosis

MORE
Start date: November 1994
Phase: Phase 3
Study type: Interventional

To study the effect of long-term treatment with raloxifene, compared with placebo, on the rate of new vertebral fractures in osteoporotic postmenopausal women with and without existing vertebral fractures.