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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT01564238 Completed - Osteoporosis Clinical Trials

Effect of Sodium Intake on Calcium Retention in Girls

Start date: January 1999
Phase: N/A
Study type: Interventional

Optimal calcium retention is important for building bone mass within the genetic potential, a key to reducing risk of osteoporosis later in life. Calcium retention is high during the rapid growth period. The investigators know that urinary calcium is affected by sodium intake but the investigators do not know the effects of sodium intake during the growth spurt or the differences in calcium retention between blacks and whites. Our hypothesis was that a high dietary sodium increases the calcium intakes required for optimal calcium retention in both black and white adolescent girls. The investigators tested calcium retention while girls consumed a low and high sodium diet during three week periods. The subjects were housed in a Purdue fraternity house during the summer and they were supervised at all times by trained staff. During the summer of 1999, subjects consumed diets with 2 levels of dietary Na+ with a fixed diet low in calcium. On the next summer, they switched to a high calcium diet. Subjects collected fecal and urine daily for 20 days. Other measurements included daily body weight, blood pressure every other day, blood sample at the end of each session. Baseline measures included bone mass, self-assessment of pubertal development, a physical examination and diet history.

NCT ID: NCT01551602 Completed - Osteoporosis Clinical Trials

Clinical Study of AK159 in Healthy Postmenopausal Women

Start date: March 2012
Phase: Phase 1
Study type: Interventional

The objective of this study is to investigate the pharmacokinetics, safety, and tolerability of AK159 administered to healthy postmenopausal women.

NCT ID: NCT01544894 Completed - Clinical trials for Postmenopausal Osteoporosis

Clinical Study of Raloxifene and Strontium Ranelate in Postmenopausal Osteoporosis

Start date: September 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study was to compare compliance and efficacy of raloxifene and strontium ranelate in a group of women with postmenopausal osteoporosis.

NCT ID: NCT01538836 Completed - Obesity Clinical Trials

Calorie Restriction, Protein Supplementation and Metabolic Health

CRPS
Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether consuming additional protein during calorie restriction induced weight loss has beneficial or harmful effects on multi-organ (liver, muscle, adipose tissue) insulin sensitivity, colonocyte proliferation rates, the gut microbiome, muscle mass and function, and bone mineral density in obese, postmenopausal women.

NCT ID: NCT01535027 Completed - Osteoporosis Clinical Trials

Combined Administration of Teripapartide and Antiresorptive Agents in Postmenopausal Osteoporosis

Confors
Start date: March 2006
Phase: Phase 4
Study type: Interventional

Increased bone formation in the absence of accelerated resorption is resulting in a marked anabolic response to teriparatide (TPTD) during the early phase after treatment initiation. Months later, due to coupling mechanism, the sustained increase of bone formation and ongoing anabolic effects are accompanied by significantly increased bone resorption as well. Antiresorptives influence the balance of bone formation and resorption. Therefore the investigators aim is to investigate the effects of the addition of antiresorptives to the second half of TPTD cycle when resorption is already also markedly elevated.

NCT ID: NCT01526278 Completed - Osteoporosis Clinical Trials

Pharmacokinetics of Maxmarvil® in Healthy Postmenopausal Women

YY_PK_2011
Start date: October 2011
Phase: Phase 1
Study type: Interventional

This study will evaluate clinical safety and pharmacokinetics of Maxmarvil® in healthy postmenopausal women

NCT ID: NCT01522521 Completed - Osteoporosis Clinical Trials

Study of AK156 in Primary Osteoporosis Patients

Start date: February 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the efficacy and safety of AK156 in Japanese patients with primary osteoporosis.

NCT ID: NCT01508169 Completed - Osteoporosis Clinical Trials

Foot Orthoses and Elderly Women With Osteoporosis

Start date: April 2011
Phase: N/A
Study type: Interventional

The objective of this study was to determine if foot orthoses are effective in improving balance, pain and disability in elderly women with osteoporosis.

NCT ID: NCT01507662 Completed - Osteoporosis Clinical Trials

Patient Activation After DXA Result Notification

PAADRN
Start date: February 2012
Phase: N/A
Study type: Interventional

There is growing evidence that patients undergoing bone mineral density testing (BMD) often do not take important steps to improve their bone health. The investigators will conduct a randomized-controlled trial to evaluate the impact of a novel and practical patient activation intervention (mailing patients their bone density test results) on the quality of bone-related healthcare and the cost-effectiveness of BMD testing. Equally important, the investigators intervention could easily be modified to include other patient populations and chronic diseases.

NCT ID: NCT01504230 Completed - Osteoporosis Clinical Trials

Multi-joint Coordination Underlies Upright Balance Control in Elderly With Osteoporosis

Start date: September 2011
Phase: N/A
Study type: Observational

Osteoporosis is a prevalent health concern among older adults and is associated with an increased risk of falls that can cause fracture, injury and even mortality. Identifying the factors related to falls occur within this population is essential for the development of effective regimes for fall prevention. The long-term objectives of this work are to ascertain the mechanisms for effectively controlling balance in seniors with osteoporosis and to provide a basis for developing fall prevention programs. The entire body's center of mass (CoM) is a critical indicator for balance control and the coordination among joints and muscles to control the CoM is still unclear. The aim1 of this study is to develop biomechanical models that control the entire body's center of mass (CoM) during upright quiet stance in seniors with osteoporosis. The aim2 of this study is to identify the mechanism to control the entire body's CoM after receiving a balance perturbation in seniors with osteoporosis. The findings of this research can provide needed information regarding the processes of balance control in this vulnerable osteoporosis population, and has the potential to be applied to individuals with other neuromuscular and orthopedic deficits.