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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT00001413 Completed - Healthy Clinical Trials

Bone Mineral Density in Women With Major Depression

Start date: April 6, 1994
Phase: N/A
Study type: Observational

The purpose of this study is to examine calcium absorption and bone mineral density in women with depression. Research indicates that pre-menopausal women with depression have significantly lower bone mineral density (BMD) than pre-menopausal women without depression. Although the mechanisms of BMD loss are unclear, researchers believe that individuals with depression have impaired calcium absorption. However, it is unknown whether the abnormal absorption is a result of depression or a side effect of the drugs used to treat it. This study will compare calcium absorption in women with depression and in healthy women without depression. Participants in this study will be given two non-radioactive calcium isotopes. One can be taken by mouth and the other must be injected. Participants will have the level of isotopes in their urine measured to estimate true fractional calcium absorption (TFCA). Participants may also have a dual X-ray absorptiometry (DEXA) scan to measure total body adiposity and lean body mass.

NCT ID: NCT00000623 Completed - Osteoporosis Clinical Trials

Thalassemia (Cooley's Anemia) Clinical Research Network (TCRN)

Start date: July 2000
Phase: N/A
Study type: Observational

The purpose of the TCRN is to accelerate research in the management of thalassemia, standardize existing treatments, and evaluate new ones in a network of clinical centers in North America. The emphasis will be on clinical trials that help identify optimal therapy. Therapeutic trials may involve investigational drugs, drugs already approved but not currently used, and drugs currently used.

NCT ID: NCT00000613 Completed - Depression Clinical Trials

CVD Risk and Health in Postmenopausal Phytoestrogen Users

Start date: April 1997
Phase: Phase 2
Study type: Interventional

To determine the acceptability and benefits of use of a dietary supplement of the phytoestrogen, genistein, versus placebo on heart disease risk factors, bone density, and psychosocial outcomes in postmenopausal women.

NCT ID: NCT00000611 Completed - Clinical trials for Cardiovascular Diseases

Women's Health Initiative (WHI)

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

To address cardiovascular disease, cancer, and osteoporosis, the most common causes of death, disability, and impaired quality of life in postmenopausal women. The three major components of the WHI are: a randomized controlled clinical trial of hormone replacement therapy (HRT), dietary modification (DM), and calcium/vitamin D supplementation (CaD); an observational study (OS); and a community prevention study (CPS). On October 1, 1997, administration of the WHI was transferred to the NHLBI where it is conducted as a consortium effort led by the NHLBI in cooperation with the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), the National Cancer Institute (NCI), and the National Institute on Aging (NIA).

NCT ID: NCT00000466 Completed - Hypertension Clinical Trials

Postmenopausal Estrogen/Progestin Interventions (PEPI)

Start date: September 1987
Phase: Phase 3
Study type: Interventional

To assess the effects of various postmenopausal estrogen replacement therapies on selected cardiovascular risk factors, including high density lipoprotein cholesterol, systolic blood pressure, fibrinogen, and insulin and on osteoporosis risk factors. Conducted in collaboration with the National Institute of Child Health and Human Development, the National Institute of Arthritis and Musculoskeletal and Skin Diseases, The National Institute of Diabetes and Digestive and Kidney Diseases, and the National Institute on Aging. The extended follow-up is for 3 years focusing on endometrium and breast evaluation.

NCT ID: NCT00000430 Terminated - Osteoporosis Clinical Trials

Low-Dose Hormone Replacement Therapy and Alendronate for Osteoporosis

Start date: October 1999
Phase: Phase 3
Study type: Interventional

Osteoporosis, a condition in which bones are fragile and break easily, is a major health problem for postmenopausal women. Research studies have shown that both estrogen/progestin replacement therapy (hormone replacement therapy, or HRT) and alendronate are effective in preventing and treating osteoporosis. However, because these drugs work in somewhat different ways, a combination of the two drugs might protect women from osteoporosis better than either drug alone. In this study we will test whether HRT and alendronate given together for 3.5 years to postmenopausal women with low bone mass will have a greater effect on bone than either HRT or alendronate given alone. We will also give every participant in this study calcium and vitamin D supplements.

NCT ID: NCT00000427 Completed - Osteoporosis Clinical Trials

Effects of Parathyroid Hormone in Men With Osteoporosis

Start date: September 1999
Phase: Phase 3
Study type: Interventional

Alendronate is a drug that blocks or reduces bone loss, while parathyroid hormone (PTH) stimulates the formation of new bone. The purpose of this study is to compare the bone-building effects of PTH alone, alendronate alone, and both PTH and alendronate in men with osteoporosis over a two-and-a-half year period.

NCT ID: NCT00000426 Completed - Osteoporosis Clinical Trials

Treatment of Calcium Deficiency in Young Women

Start date: January 1995
Phase: Phase 2
Study type: Interventional

This study looks at the effects of calcium supplementation on bone density in women in their third decade of life. We placed women aged 19-27 who take in low amounts of calcium in their diets in one of two groups. We will give women in one group a placebo (inactive pill) and women in the other group 1500 milligrams of calcium per day (as calcium carbonate). We will monitor the results by looking at the change in bone mineral density measured at the hip, total body, forearm, and spine. Treatment will last 3 years.

NCT ID: NCT00000413 Completed - Osteoporosis Clinical Trials

Osteoporosis Prevention in Preadolescent Girls

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

This study will test an osteoporosis prevention program aimed at preadolescent girls between the ages of 10 and 12 who have not yet started their menstrual periods. Girls in this age group are adding large amounts of new bone to their skeletons. Adding more bone at this time of life can reduce a person's chances of developing osteoporosis (thinning bones) in later years. We will look at how this osteoporosis prevention program affects the amount of calcium in the girls' diets, the amount of weight-bearing exercise they do, and their bone mass measured using ultrasound testing of the heel.

NCT ID: NCT00000412 Completed - Osteoporosis Clinical Trials

Osteoporosis Prevention After Heart Transplant

Start date: September 1997
Phase: Phase 3
Study type: Interventional

During the first year after a heart transplant, people often rapidly lose bone from their spine and hips. About 35 percent of people who receive heart transplants will suffer broken bones during the first year after transplantation. This study will compare the safety and effectiveness of the drug alendronate (Fosamax) and the active form of vitamin D (calcitriol) in preventing bone loss at the spine and hip after a heart transplant. In this study, people who have had a successful heart transplant will receive either active alendronate and a "dummy pill" instead of calcitriol, or active calcitriol and a dummy pill instead of alendronate for the first year after their transplant, starting within 1 month after transplant surgery. We will measure bone density in the hip and spine at the start of the study and after 6 and 12 months, and will also check for broken bones in the spine. This research should lead to ways of preventing this crippling form of osteoporosis.