Clinical Trials Logo

Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

Filter by:

NCT ID: NCT00222872 Completed - Osteoporosis Clinical Trials

3-Week Parathyroid Hormone-related Protein (PTHrP) Dose Escalation Study in Post-Menopausal Women

Start date: July 2005
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to determine the safety and effectiveness of three week daily subcutaneous injections of Parathyroid Hormone-related Protein (1-36). Previous studies indicated that PTHrP has a skeletal 'anabolic' or bone-building effect, and has shown to increase bone mineral density in postmenopausal women with osteoporosis. Safety of PTHrP will be determined by measurements of blood pressure and pulse, serum blood calcium levels and subjective symptoms. Effectiveness will be measured by changes in measurements of blood and urine markers of bone turnover.

NCT ID: NCT00221299 Completed - Osteoporosis Clinical Trials

Risedronate and Parathyroid Hormone to Reverse Osteoporosis Caused by Chronic Steroid Use

Start date: September 2005
Phase: Phase 4
Study type: Interventional

The purpose of the study is to learn if one year of treatment with parathyroid hormone (PTH), either alone or with risedronate, will increase the thickness of the bones in the hip and spine in subjects with osteoporosis from chronic low dose steroid use. During the second year, the study will also look at whether taking risedronate will preserve the bone thickness created by one year of rhPTH 1-34 treatment.

NCT ID: NCT00212719 Completed - Clinical trials for Involutional Osteoporosis

Controlled Study of ONO-5920 in Patients With Involutional Osteoporosis in Japan

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

The purpose of this study is to evaluate the efficacy and safety of ONO-5920 in patients with involutional osteoporosis.

NCT ID: NCT00212667 Completed - Clinical trials for Involutional Osteoporosis

Controlled Study of ONO-5920 in Patients With Involutional Osteoporosis in Japan

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

The purpose of this study is to evaluate the efficacy and safety of ONO-5920 in patients with involutional osteoporosis.

NCT ID: NCT00212628 Completed - Clinical trials for Involutional Osteoporosis

Controlled Study of ONO-5920 in Patients With Involutional Osteoporosis in Japan

Start date: June 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of ONO-5920 in patients with involutional osteoporosis.

NCT ID: NCT00211211 Completed - Multiple Myeloma Clinical Trials

FREE Study - Fracture Reduction Evaluation

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

The primary objective of this study is to compare the effectiveness of standard medical therapy alone to kyphoplasty using the KyphX system for the treatment of acute vertebral body compression fractures.

NCT ID: NCT00209469 Active, not recruiting - Osteoporosis Clinical Trials

Network Osteoporosis Study

Start date: July 2002
Phase: Phase 2/Phase 3
Study type: Interventional

This study is evaluating the use of the drug alendronate in preventing or reversing bone loss in children and adolescents receiving steroid medications.

NCT ID: NCT00205777 Completed - Osteoporosis Clinical Trials

Study Evaluating Bazedoxifene Acetate In Osteoporosis In Postmenopausal Women

Start date: December 2001
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether bazedoxifene acetate is safe and effective in the treatment of osteoporosis in postmenopausal women.

NCT ID: NCT00204919 Completed - Osteoporosis Clinical Trials

Vitamin D Administration in the Nursing Home

Start date: June 2001
Phase: N/A
Study type: Interventional

Administration of vitamin D 50,000 units once monthly will: - Maintain serum 25-OH vitamin D above 20 ng/ml - Reduce falls - Increase calcaneal BMD - Reduce bone turnover - Be well tolerated: volunteers will not develop hypercalcemia - Improve performance on a swallowing quality of life questionnaire

NCT ID: NCT00204425 Completed - Osteoporosis Clinical Trials

Effect of Exercise Training and Soy-based Nutritional Supplementation on Prevention of Osteoporosis

Start date: December 2004
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine the effectiveness of combining exercise training (i.e. weight lifting and walking) and dietary supplementation with a soy-based nutritional supplement for increasing bone mineral density. We hypothesize that the exercise training and soy-based supplement will be additive for increasing bone mineral density.