Clinical Trials Logo

Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

Filter by:

NCT ID: NCT00447915 Completed - Clinical trials for Primary Osteoporosis

Phase II/III Clinical Study of R484iv (Ibandronic Acid) for Primary Osteoporosis

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

To evaluate the efficacy and safety of R484iv by intravenous intermittent administration to patients with primary osteoporosis in comparison with sodium risedronate hydrate (RIS) by oral administration every day. To evaluate also the dose response of R484iv.

NCT ID: NCT00443716 Completed - Osteoporosis Clinical Trials

Determination of Adipocyte Parameters in Iliac Crest Biopsies From Post Menopausal Women

Start date: April 1985
Phase: N/A
Study type: Interventional

To evaluate the effect of estrogen treatment on adipocytic and osteoblastic parameters by histomorphometrically measuring adipocyte volume (AV/TV) and adipocyte numbers in goldner's stained iliac crest bone biopsy specimens collected from subjects recruited in the study (IRB number 21B85). The adipocytic parameters will be then correlated with osteoblastic parameters obtained previously during the course of the initai study involving the effect of transdermal estrogen on bone turnover in postmenopausal osteoporotic women.

NCT ID: NCT00439647 Completed - Male Osteoporosis Clinical Trials

Efficacy in Reducing Fractures and Safety of Zoledronic Acid in Men With Osteoporosis

Start date: December 2006
Phase: Phase 3
Study type: Interventional

This study will investigate if the drug zoledronic acid given once yearly is safe and has beneficial effects in treating osteoporosis by reducing bone loss and fractures in men with osteoporosis.

NCT ID: NCT00439244 Completed - Osteoporosis Clinical Trials

Efficacy Study of Zoledronic Acid and Teriparatide Combination Therapy in Women With Osteoporosis

Start date: December 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the effects of zoledronic acid administered at the same time with teriparatide compared to zoledronic acid alone and teriparatide alone on bone mineral density (BMD) gain in the lumbar spine and total hip

NCT ID: NCT00436917 Completed - Breast Cancer Clinical Trials

Zoledronate in Treating Osteopenia or Osteoporosis in Postmenopausal Women Receiving Letrozole for Stage I, Stage II, or Stage IIIA Primary Breast Cancer

Start date: April 2006
Phase: N/A
Study type: Interventional

RATIONALE: Zoledronate may reduce bone loss in patients receiving letrozole for breast cancer. PURPOSE: This clinical trial is studying how well zoledronate works in treating osteopenia or osteoporosis in postmenopausal women receiving letrozole for stage I, stage II, or stage IIIA primary breast cancer.

NCT ID: NCT00433160 Completed - Osteoporosis Clinical Trials

Phase 3 Clinical Trial of Teriparatide in Japan

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

To evaluate the efficacy of teriparatide based on measurements of bone mineral density at lumbar spine

NCT ID: NCT00432692 Completed - Osteoporosis Clinical Trials

Falls Prevention in Osteoporosis

Start date: December 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine wether a falls prevention program can reduce fall incidence in people with osteoporosis.

NCT ID: NCT00431444 Completed - Osteoporosis Clinical Trials

Effects of Zoledronic Acid and Raloxifene on Bone Turnover Markers in Postmenopausal Women With Low Bone Mineral Density

Start date: January 2007
Phase: Phase 4
Study type: Interventional

This study will compare the effects of Zoledronic acid and Raloxifene in reducing bone turnover markers in postmenopausal women with low bone mineral density over 6 months.

NCT ID: NCT00421408 Completed - Osteoporosis Clinical Trials

The Effect of Protein Supplementation on Bone Health in Healthy Older Men and Women

Start date: February 2007
Phase: Phase 1/Phase 2
Study type: Interventional

Women and men consuming a low protein diet may be at risk for bone loss. The purpose of this study is to determine whether a daily protein supplement will improve bone health among healthy older adults.

NCT ID: NCT00421343 Completed - Osteoporosis Clinical Trials

Secondary Prevention of Osteoporosis

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

The purpose of this study is to develop and implement an evidence based protocol for the secondary prevention of osteoporotic fractures and falls, and to determine how compliance with this intervention improves muscle strength and functional status following a fracture.