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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT00665860 Completed - Osteoporosis Clinical Trials

Safety and Effectiveness of Soy Phytoestrogens to Prevent Bone Loss

OPUS
Start date: April 2001
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether soy isoflavone supplementation is safe and effective to prevent bone loss in postmenopausal women.

NCT ID: NCT00665613 Completed - Osteoporosis Clinical Trials

The Relationship Between Osteoporosis and Chronic Oral Anticoagulation Therapy With Warfarin

Start date: October 2004
Phase: N/A
Study type: Observational

The purpose of this study is to determine if osteoporosis is an unrecognized complication of chronic anticoagulation with warfarin.

NCT ID: NCT00664053 Completed - Osteoporosis Clinical Trials

Effects of DHEA/Exercise on Bone, Muscle and Balance

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

The purpose of this study is to examine whether muscle strength and balance will improve in women with frailty selected for dehydroepiandrosterone sulfate (DHEAS) levels below 550 ng/dl treated with DHEAS supplementation and Hatha yoga. Investigators believe the effects of both treatments will improve outcomes more than either treatment alone and may be additive; in addition, lean body mass, skeletal muscle mass, markers of bone turnover and physical performance will improve following treatment with DHEA and/or yoga.

NCT ID: NCT00663221 Completed - Osteoporosis Clinical Trials

Study of the Osteoprotector Effects of a Milk Product Based on Anthocyans and Enriched in Calcium and Vitamin D

Start date: March 2008
Phase: Phase 2
Study type: Interventional

We hypothesize that anthocyans with calcium and vitamin D have a positive effect on bone reshaping in menopausal women.

NCT ID: NCT00663143 Completed - Osteoporosis Clinical Trials

Thiazolidinediones (TZD) Bone Loss and the Effects on Bone Marrow Differentiation and Osteoblast Formation

TZDBONE
Start date: July 2009
Phase: N/A
Study type: Observational

Thiazolidinediones (TZDs) are a commonly used antidiabetic drugs currently used by over a million patients in the United States. Recent studies have shown that treatment with TZD may increase the risk of bone fractures. The cause of bone loss is not known. We believe that TZD may cause increased accumulation of fat in the bone marrow, which may cause decrease bone formation and weak bones. .

NCT ID: NCT00661856 Completed - Osteoporosis Clinical Trials

Effect of Soy Isoflavones on Bone Mineral Density and Physical Performance Indices

SoyPTI
Start date: January 2001
Phase: N/A
Study type: Interventional

The aim of the present study was to investigate the effects of soy and soy plus isoflavones on bone mineral Density and physical performance in post menopausal women.

NCT ID: NCT00660686 Completed - Osteoporosis Clinical Trials

Exercise for Physical Health in Men With Prostate Cancer

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

The purpose of this study is to conduct a 12-month randomized controlled trial comparing the effects of strength and impact exercise training to flexibility/relaxation training on body composition (bone, muscle and fat mass), physical function (strength, gait, power, balance and self-report physical function and symptoms) in men currently treated with hormone therapy for prostate cancer.

NCT ID: NCT00655681 Completed - Cerebral Palsy Clinical Trials

Prevention of Post Operative Bone Loss in Children

Start date: September 2007
Phase: N/A
Study type: Interventional

Hypothesis: one-dose pamidronate will prevent post-operative bone loss in children at risk for low bone density Plan: children with chronic disease such as CP, spina bifida, etc. will be recruited pre operatively and studied with DXA scan. After surgery, children will be randomized to receive either pamidronate or saline. Repeat DXA scan will determine bone lost after end of immobilization or nonweightbearing.

NCT ID: NCT00655577 Completed - Osteoporosis Clinical Trials

Exercise and Prevention of Hip Fractures

Start date: August 1998
Phase: N/A
Study type: Interventional

The significance of this population-based study is in producing new information for planning interventions and rehabilitation programs for the elderly, planning education of health care personnel and planning national health education programs for different age groups. The study consists of an epidemiological cross-sectional study and a randomized controlled intervention study. The study population consisted of all the 1689 home-dwelling women born during 1924-1927 residing in Oulu, Northern Finland, who were asked to a screening visit including bone mineral density (BMD) measurement of the distal radius in 1997. 1222 women attended the clinic and were afterwards mailed a postal questionnaire focusing on lifelong risk factors for osteoporosis, e.g. the amount of physical activity at work and during leisure time, daily intake of calcium and use of alcohol and cigarettes. Those with BMD value more than 20% lower than the reference value, underwent a densitometry of the hip. All women with femoral neck BMD more than 20% below the reference value (n=160) were randomly selected to either exercise (n=84) or control (n=76) group. At baseline and after that annually during the 30-month intervention, balance, muscle strength, aerobic capacity, walking speed, cognitive functions and mood are measured from all the participants. Hip BMD will be measured annually. The exercise group participates in a supervised training program with weekly sessions from the beginning of October to the end of April. In addition to the supervised sessions the participants train daily at home. From April to October the exercises are performed purely at home. The training regimen consists of balance, strength and impact exercises. The intervention group keeps diary of their daily physical activity. The number and severity of falls are recorded from both the groups. The purpose of the study is: 1. to identify factors accounting for low BMD in elderly home-dwelling women with severe osteopenia. 2. to evaluate how supervised regular weight-bearing exercise program affects BMD in elderly home-dwelling women with severe osteopenia 3. to evaluate how supervised regular balance and muscle training affects balance and muscle strength in elderly home-dwelling women with severe osteopenia. In addition the aim is to: 4. study how regular supervised exercise affects the incidence and severity of falls, mood and cognitive functions in women with severe osteopenia. Hypothesis and research methods The main hypothesis is that long-term supervised, mainly home- based regular impact-type and balance and muscle exercises can improve balance and muscle strength of lower extremities and maintain bone mass in elderly women. We also hypothesize that the incidence of falls is lower in the exercise group than in the controls and that the falls are more injurious in the control group than in the intervention group during the follow-up period

NCT ID: NCT00651534 Completed - Osteoporosis Clinical Trials

To Estimate Relative Bioavailability of 5 Formulations of Ronacaleret Given to Healthy Postmenopausal Females

Start date: February 2008
Phase: Phase 1
Study type: Interventional

This study will examine the effects of formulation on the relative bioavailability of SB-751689 (400 mg) administered to healthy postmenopausal women. Subjects will receive a single oral dose of each formulation, with five formulations of SB-751689 tested in total. Blood samples will be taken up to 24 hours postdose after each dose administration. This study will provide information for future possible formulation development of SB-751689 for Phase III.