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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT00081653 Completed - Clinical trials for Post-Menopausal Osteoporosis

A Study of Bonviva (Ibandronate) in Women With Post-Menopausal Osteoporosis Previously Treated With Bonviva

Start date: May 2004
Phase: Phase 4
Study type: Interventional

This 2 arm study will assess the long-term efficacy and safety of oral treatment with 100mg or 150mg Bonviva in women with post-menopausal osteoporosis who have previously completed Bonviva study BM16549 (MOBILE study). Patients will receive Bonviva either 100mg po monthly, or 150mg po monthly. 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: NCT00079924 Completed - Clinical trials for Postmenopausal Osteoporosis

Effects of Teriparatide in Postmenopausal Women With Osteoporosis

Start date: November 2004
Phase: Phase 4
Study type: Interventional

Effects of Teriparatide in Postmenopausal Women Previously Treated with Alendronate or Raloxifene.

NCT ID: NCT00079521 Completed - Osteoporosis Clinical Trials

Therapeutic Touch for Wrist Fractures in Postmenopausal Women

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

This study will evaluate the effectiveness of therapeutic touch in treating wrist fractures in women past menopause.

NCT ID: NCT00079248 Active, not recruiting - Breast Cancer Clinical Trials

Hormone Replacement Therapy in Relieving Menopausal Symptoms in Postmenopausal Women With Previous Stage I or Stage II Breast Cancer

Start date: March 2002
Phase: N/A
Study type: Interventional

RATIONALE: Hormone replacement therapy may be effective in relieving symptoms of menopause, such as hot flashes, night sweats, and vaginal dryness, without causing a recurrence of breast cancer. PURPOSE: This randomized clinical trial is studying hormone replacement therapy to see how well it works in relieving symptoms of menopause in postmenopausal women with previous stage I or stage II breast cancer.

NCT ID: NCT00078026 Terminated - Osteoporosis Clinical Trials

An Investigation Into the Short Term Effect of APOMINE in Patients With Osteoporosis or Low Bone Mass

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

Osteoporosis affects millions of postmenopausal women in the USA. The current approved treatments are all drugs that prevent bone loss and possibly result in small gains in bone mass. Another possible treatment consists of drugs that increase bone formation. There are currently two drugs that stimulate bone formation, sodium fluoride and human parathyroid hormone (hPTH). Neither of these two drugs has been approved by the FDA. APOMINE has shown significant bone formation in animal studies. In this study we plan to test whether APOMINE is able to stimulate new bone formation in women with osteoporosis or low bone mass.

NCT ID: NCT00076050 Active, not recruiting - Osteoporosis Clinical Trials

Using Soy Estrogens to Prevent Bone Loss and Other Menopausal Symptoms

SPARE
Start date: September 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if soy-derived phytoestrogens (naturally occurring compounds similar to estrogen) can prevent bone loss and other menopausal symptoms in women who have recently gone through menopause. Study hypothesis: Tablets of high-dose, purified soy phytoestrogens spare the normally occurring spinal bone loss and improve biological and other emotional changes of menopause.

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: NCT00073190 Completed - Osteoporosis Clinical Trials

Patient- and Physician-Based Osteoporosis Education

Start date: September 2003
Phase: Phase 1
Study type: Interventional

Osteoporosis is an important public health problem. Osteoporosis can cause serious health complications and death and leads to increased medical costs. The purpose of this study is to identify an effective method of educating patients and health care professionals about the diagnosis and treatment of osteoporosis.

NCT ID: NCT00070681 Completed - Clinical trials for Cardiovascular Diseases

Outcomes of Sleep Disorders in Older Men

Start date: September 2003
Phase: Phase 3
Study type: Observational

To determine the effects of sleep disorders on cardiovascular function and disease in older men.

NCT ID: NCT00069173 Recruiting - Osteoporosis Clinical Trials

Preventing Osteoporosis in Adolescent Girls

Start date: July 2000
Phase: Phase 1
Study type: Interventional

Physical activity in adolescents is an important part of bone health. Good bone health in adolescents can decrease the risk of osteoporosis. This study will evaluate a program designed to increase the level of physical activity in adolescent girls.