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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT01690000 Completed - Osteoporosis Clinical Trials

Treatment of Osteopenia With Melatonin

MelaOst
Start date: November 2012
Phase: N/A
Study type: Interventional

The aim of the study is to assess the effect of melatonin treatment in patients with osteopenia on BMD, muscle function, quality of life and calcium homeostasis.

NCT ID: NCT01679899 Completed - Clinical trials for Type 2 Diabetes Mellitus

Effect of Anti-diabetic Drugs on Bone Metabolism and Glycemic Variability

BoneGlyc
Start date: December 2012
Phase: Phase 4
Study type: Interventional

This is a Monocentric, Prospective, Randomized, Open-label, Comparative, Phase IV Study, to compare the effects of Vildagliptin and Gliclazide MR on Markers of Bone Remodeling, Bone Mineral Density and Glycemic Variability in Postmenopausal Women with Type 2 Diabetes. A total of 38 women with documented Type 2 Diabetes and menopause will be enrolled. The active treatment will include a 50 mg dose of vildagliptin OD twice a day. As comparator, gliclazide MR will be administered at a dose of 60 to 120 mg OD once a day.

NCT ID: NCT01677637 Completed - Osteoporosis Clinical Trials

Osteoporosis Screening Trial

OSTRIA
Start date: February 2012
Phase: N/A
Study type: Observational

Osteoporosis is the most common disease of bone and characterized firstly by low bone mass and secondly, impaired bone microarchitecture structure resulting in reduced strength and increased risk of fracture. Osteoporosis is divided into: primary (Postmenopausal Osteoporosis Osteoporosis & elderly and senile osteoporosis) and secondary. The most common form is postmenopausal osteoporosis. It occurs in women after menopause and is associated with decreased estrogen production, which normally occurs at this age women Osteoporosis usually occurs after age 50, it is very common in women than in men, and its frequency increases with advancing age.

NCT ID: NCT01675297 Completed - Osteoporosis Clinical Trials

Efficacy and Safety Study of Risedronate, Cholecalciferol Combination Tablet in Patients With Osteoporosis

Start date: July 4, 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy and the safety of Risedronate, cholecalciferol combination tablet in patients with Osteoporosis.

NCT ID: NCT01674621 Completed - Clinical trials for Post Menopausal Osteoporosis

Phase 2 Study of BA058 (Abaloparatide) Transdermal Delivery in Postmenopausal Women With Osteoporosis

Start date: September 25, 2012
Phase: Phase 2
Study type: Interventional

To determine the clinical safety and efficacy of abaloparatide transdermal in otherwise healthy postmenopausal women with osteoporosis as assessed by changes in bone mineral density (BMD) and serum markers of bone metabolism when compared to transdermal placebo and abaloparatide injection for 6 months of treatment.

NCT ID: NCT01669954 Completed - Osteoporosis Clinical Trials

Determination of Optimum Age for DXA Screening for Osteoporosis in HIV - The Probono 1 Study

Probono1
Start date: February 2009
Phase: N/A
Study type: Observational

The purpose of this study is to determine the bone mineral density in male and female patients with HIV infection according to age groups. This will enable a practical approach to screening for osteoporosis and the management and prevention of fragility fractures in people with HIV. In addition, all risk factors commonly associated with fragility fractures and osteoporosis are collected, as is HIV drug history. Hence, as secondary outcomes, the associations with reduced bone mineral density can be ascertained.

NCT ID: NCT01668589 Completed - Clinical trials for Postmenopausal Osteoporosis

Observational Study of Denosumab (Prolia®) in Postmenopausal Women With Osteoporosis

Start date: November 28, 2011
Phase: N/A
Study type: Observational

The main objective of this observational study was to describe medication-taking behavior of patients treated with denosumab for postmenopausal osteoporosis (PMO) at 12 and 24 months.

NCT ID: NCT01666522 Completed - Sarcopenia Clinical Trials

Vitamin D and Physical Activity for Prevention of Sarcopenia in Osteoporosis

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

In the present study the aim was to determine the prevalence of sarcopenia and to evaluate the effectiveness of an exercise program and vitamin D supplementation in enhancing muscle mass and strength in community-dwelling older adults with osteopenia /osteoporosis. One hundred and forty-five individuals aged 65 years and above with documented osteopenia/osteoporosis were scanned for sarcopenia. The participants were randomly assigned to one of four groups: Group 1-PA and vitamin D (n= 38), Group 2-PA(n=36), Group 3-vitamin D (n= 36) or Group 4-healthy lifestyle(n =35) for 16 weeks. The PA group received a 60-minute 3-day/week exercise programme, the vitamin D group received oral cholecalciferol 2000 IU/day and the control group was provided with health education using videotaped presentations, physician talks on topics concerning bone and muscle health. Body composition was measured DEXA. Vitamin D levels were measured and PA was measured using the Baecke Physical Activity Questionnaire. Physical performance was assessed using upper limb grip strength, walking speed and knee extension strength. All data was collected at baseline and at 4 months.

NCT ID: NCT01663129 Completed - Clinical trials for Acute Lymphoblastic Leukemia

Steroid-Induced Osteoporosis in the Pediatric Population - Canadian Incidence Study

STOPP-CIS
Start date: January 2005
Phase:
Study type: Observational

To determine the magnitude and rate of bone mass deficits following initiation of glucocorticoid therapy for the treatment of pediatric leukemia, rheumatic conditions and nephrotic syndrome, we propose a 6 year, prospective study in 12 academic, tertiary care centres across Canada. The investigators hypothesize that glucocorticoid-treated children with leukemia, rheumatic conditions and nephrotic syndrome will fail to accrue bone mass at a normal rate, and that deficits in mineral accrual will occur in a glucocorticoid dose- and duration-dependent fashion. We also hypothesize that the fracture incidence will increase with concomitant reductions in bone mass.

NCT ID: NCT01660503 Completed - Osteoporosis Clinical Trials

Dose Effects of SCF on Calcium Metabolism and GI Microflora in Adolescents

Start date: June 1, 2012
Phase: N/A
Study type: Interventional

Soluble corn fiber (SCF) has been shown to enhance calcium utilization and bone properties in rats and in adolescent boys and girls.