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Osteoporosis, Postmenopausal clinical trials

View clinical trials related to Osteoporosis, Postmenopausal.

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NCT ID: NCT00048061 Completed - Clinical trials for Post Menopausal Osteoporosis

MOBILE Study - A Study of Bonviva (Ibandronate) Regimens in Women With Post-Menopausal Osteoporosis

Start date: April 2002
Phase: Phase 3
Study type: Interventional

This study will compare the efficacy and safety of different treatment regimens of oral Bonviva tablets in women with post-menopausal osteoporosis. Patients will also receive daily supplementation with vitamin D and calcium. The anticipated time of study treatment is 2+ years, and the target sample size is 500+ individuals.

NCT ID: NCT00046137 Completed - Clinical trials for Osteoporosis, Postmenopausal

Combined Use of Teriparatide and Raloxifene in Postmenopausal Women With Osteoporosis

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare treatment with both teriparatide and raloxifene with teriparatide alone. The study will evaluate any side effects that may be associated with the two drugs and may help to determine whether teriparatide and raloxifene together can help patients with osteoporosis more than teriparatide alone.

NCT ID: NCT00035256 Completed - Clinical trials for Osteoporosis, Postmenopausal

Sequential Use of Teriparatide and Raloxifene HCl in the Treatment of Postmenopausal Women With Osteoporosis

Start date: October 2001
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the increase in spine bone mineral density that has been generally observed in previous clinical studies involving the study drug can be maintained or even increased if followed with raloxifene HCl. All qualifying study participants will receive the study drug followed by treatment with raloxifene HCl or placebo. All study participants will receive raloxifene HCl in the third phase of the study.

NCT ID: NCT00018447 Completed - Clinical trials for Osteoporosis, Post-Menopausal

Combination Osteogenic Therapy in Established Osteoporosis

Start date: November 1998
Phase: Phase 2
Study type: Interventional

This study is designed to determine if combining parathyroid (PTH 1-34) with fluoride (MFPSR) therapy in a cyclic treatment regimen will: (1) produce a greater increase in bone density of the spine than would be produced by either treatment alone; (2) prevent the resistance (i.e., decreased bone formation and no further increase in bone density) that is observed within 18-24 months of PTH therapy; (3) eliminate the calcium deficiency and osteomalacia that can occur with fluoride; (4) prevent excessive bone fluoride content; and (5) result in an increase in bone density which is maintained after treatment is discontinued.

NCT ID: NCT00010712 Completed - Hot Flashes Clinical Trials

Effects of Black Cohosh on Menopausal Hot Flashes

Start date: September 1999
Phase: Phase 2
Study type: Interventional

This study will assess whether treatment with black cohosh is effective in reducing the frequency and intensity of menopausal hot flashes. In addition, this study will determine whether or not black cohosh reduces the frequency of other menopausal symptoms and improves quality of life.