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Osteopenia clinical trials

View clinical trials related to Osteopenia.

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NCT ID: NCT00145977 Completed - Osteoporosis Clinical Trials

Texture Analysis for Postmenopausal Osteoporosis

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

The purpose of this study is to determine if a new test for osteoporosis can be useful in monitoring treatment. We are studying a new method for examining the quality of bone by an experimental method of computerized analysis of radiographic images (x-ray pictures) of the heel.

NCT ID: NCT00145275 Completed - Osteopenia Clinical Trials

To Assess the Efficacy of Over-the-counter Analgesics in the Prevention/Treatment of Transient Post-dose Symptoms Following Zoledronate Infusion in Post-menopausal Women

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

Zoledronic acid is a medicine being studied in people with low bone mass. Side effects such as headache, fever, muscle aches, and pains, may occur following the infusion. This study will investigate the use of over-the-counter medicines to improve these symptoms.

NCT ID: NCT00132808 Completed - Osteopenia Clinical Trials

Zoledronic Acid in the Prevention of Bone Loss in Postmenopausal Women With Osteopenia, 45 Years of Age and Older

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

Osteoporosis prevention is important in patients with osteopenia (low bone density). This study will test the safety and efficacy of zoledronic acid in patients diagnosed with osteopenia.

NCT ID: NCT00108394 Completed - Osteopenia Clinical Trials

Osteopenia and Renal Osteodystrophy: Evaluation and Management

Start date: October 2002
Phase: Phase 4
Study type: Interventional

The purpose of this study is to demonstrate whether pamidronate will preserve or increase bone mass in patients with adynamic bone disease, caused by low bone turnover.

NCT ID: NCT00089661 Completed - Breast Cancer Clinical Trials

AMG 162 in the Treatment of Bone Loss in Subjects Undergoing Aromatase Inhibitor Therapy for Non-metastatic Breast Cancer

Start date: October 1, 2004
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to evaluate AMG 162 in the treatment of bone loss in subjects undergoing Aromatase Inhibitor Therapy for Non-metastatic Breast Cancer.

NCT ID: NCT00074711 Completed - Osteoporosis Clinical Trials

Adding Phosphorus to Osteoporosis Drug Treatment

Start date: August 2004
Phase: Phase 2
Study type: Interventional

Osteoporosis causes bones to weaken and break more easily. Calcium and phosphorus are two minerals that are essential for normal bone formation. Unfortunately, calcium salts commonly prescribed in anti-osteoporosis treatment bind phosphorus from food and restrict phosphorus available for bone building. Teriparatide is a drug that reduces the risk of fractures by increasing bone thickness and strength. Vitamin D is also necessary for strong bones and teeth. The purpose of this study is to evaluate the bone-building effectiveness of two calcium supplements, one with a source of phosphorus and one without, in combination with teriparatide and vitamin D in women with osteoporosis.

NCT ID: NCT00069004 Completed - HIV Infections Clinical Trials

A Study of Physical and Metabolic Abnormalities in HIV Infected and Uninfected Children and Youth

Start date: October 2003
Phase: N/A
Study type: Observational

The purpose of this study is to assess the prevalence of metabolic and physical abnormalities in HIV infected (via mother-to-child transmission) and uninfected children and youth. Metabolism, body composition, bone density, and other factors will be assessed in relationship to participants' exposure to highly active antiretroviral therapy (HAART).

NCT ID: NCT00067834 Completed - Osteopenia Clinical Trials

Electromagnetic Treatment For Bone Loss After Forearm Fracture

Start date: November 2003
Phase: Phase 1/Phase 2
Study type: Interventional

This study will determine the usefulness of pulsing electromagnetic field (PEMF) technology to reverse or reduce the bone loss (osteopenia) that occurs in the forearm after fracture or surgery.

NCT ID: NCT00065637 Completed - Osteoporosis Clinical Trials

Once Weekly Parathyroid Hormone for Osteoporosis

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

Daily parathyroid hormone (PTH) is approved by the FDA for the treatment of osteoporosis. This study will evaluate the safety and effectiveness of PTH when given once a week.

NCT ID: NCT00043745 Completed - Osteoporosis Clinical Trials

Bone Response to Soy Isoflavones in Women

SIRBL
Start date: March 2003
Phase: Phase 2
Study type: Interventional

This study will provide valuable data on whether soy isoflavones impact bone loss in postmenopausal women. The study will help clarify potential mechanisms and contribute to our understanding of isoflavones as an alternative to traditional hormone therapy.