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Osteoporosis, Postmenopausal clinical trials

View clinical trials related to Osteoporosis, Postmenopausal.

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NCT ID: NCT02014467 Completed - Clinical trials for Osteoporosis, Postmenopausal

Denosumab China Phase III Study

Start date: January 2014
Phase: Phase 3
Study type: Interventional

This study is to evaluate the efficacy and safety of denosumab 60mg for 12 month treatment in Chinese postmenopausal women with osteoporosis at increased risk of fracture.

NCT ID: NCT01992159 Completed - Clinical trials for Postmenopausal Osteoporosis (PMO)

Efficacy, Safety and Tolerability of Romosozumab in the Treatment of Japanese Women With Postmenopausal Osteoporosis

Start date: October 12, 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if treatment with romosozumab increases bone mineral density in Japanese women with postmenopausal osteoporosis.

NCT ID: NCT01969656 Completed - Clinical trials for Postmenopausal Osteoporosis, Multiple Sites

Safety Study of an Oral Vitamin D Analog in Postmenopausal Women

Start date: n/a
Phase: Phase 1
Study type: Interventional

Determine the safety of 2MD, a vitamin D analog, when administered orally once daily for 28 days in healthy normal postmenopausal women.

NCT ID: NCT01945788 Active, not recruiting - Clinical trials for Postmenopausal Osteoporosis With Pathological Fracture

Clinical Comparison of Efficacy and Safety of Two Teriparatide Formulations: Osteofortil and Forteo

Start date: June 2013
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to compare efficacy and safety of two formulations of teriparatide 20 mcg/day plus calcium and vitamin D in postmenopausal women with osteoporosis.

NCT ID: NCT01881204 Completed - Clinical trials for Osteoporosis, Postmenopausal

Hesperidin and Bone Health in Postmenopausal Women

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

The primary objective of this clinical trial is to test hesperidin with and without CALCILOCK® for bone resorption suppressing effect in postmenopausal women. The secondary objective is the comparison between 41Ca technology and classical biomarker to evaluate bone resorption.

NCT ID: NCT01834105 Recruiting - Clinical trials for Postmenopausal Osteoporosis

Molecular Mechanism of POP Kidney Yin Deficiency Syndrome From the Interventional Effects of CLCF1

pop
Start date: January 2012
Phase: Phase 2
Study type: Interventional

This study use RT-PCR and Western Blot technique to detect the expression of CLCF1 mRNA and protein in POP Kidney Yin deficiency group and healthy group to verify the relevance between CLCF1 and POP the kidney Yin deficiency syndrome.Through siRNA and overexpression,observe the mRNA and protein 's expression of CBP、JAK1、STAT4 and the protein phosphorylation of JAK1、STAT4 in JAK-STAT signal to reveal the CLCF1 regulate the CBP's mechanism.Use the Liuwei Dihuang Pills to detect the effect of treatment ,compare use or not the Liuwei Dihuang Pills to detect the mRNA and protein 's expression of CLCF1、CBP etc.Aim to clarify the POP kidney Yin deficiency molecular mechanism.

NCT ID: NCT01826656 Withdrawn - Clinical trials for Post-menopausal Osteoporosis

Bone Healing in Healthy and Post-menopausal Osteoporotic Women

Start date: May 2014
Phase: N/A
Study type: Interventional

Both the pathogenesis and the treatment of osteoporosis may potentially interfere at different levels on the multi-stage complex cascade of events involved in bone healing/regeneration. To our knowledge no human studies have been performed to clarify the potential effect of osteoporosis on post-extraction alveolar healing. The primary outcome of the study is to compare alveolar bone changes in width and height 3 months after tooth extraction in 10 post-menopausal osteoporotic women and 10 post menopausal non osteoporotic women by the use of cone-beam computer tomography (CBCT) images. The secondary outcomes considered are: clinical changes in the external contour of the ridge and periodontal parameters in the neighbouring teeth after a tooth extraction and 3 months later. In addition the accuracy of panoramic morphometric indexes in detecting osteoporosis will be measured.

NCT ID: NCT01796301 Completed - Clinical trials for Postmenopausal Osteoporosis

An Open-label Study to Evaluate the Effect of Treatment With Romosozumab or Teriparatide in Postmenopausal Women

STRUCTURE
Start date: January 31, 2013
Phase: Phase 3
Study type: Interventional

The primary objective of the study was to evaluate the effect of 12 months of treatment with romosozumab compared with teriparatide on total hip bone mineral density (BMD) in postmenopausal women with osteoporosis who were previously treated with bisphosphonate therapy.

NCT ID: NCT01760798 Recruiting - Osteoporosis Clinical Trials

Weekly vs Daily Teriparatide Therapy in Severe Postmenopausal Osteoporosis

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

Osteoporosis is characterized by decreased bone strength and it is prevalent among postmenopausal women but also occurs in men and women with underlying conditions or major risk factors associated with bone demineralization. Its chief clinical manifestations are vertebral and hip fractures, although fractures can occur at any skeletal site.The World Health Organization (WHO) operationally defines osteoporosis as a bone density that falls 2.5 standard deviations (SD) below the mean for young healthy adults of the same gender—also referred to as T-score of -2.5. Postmenopausal women who fall at the lower end of the young normal range (a T-score of >1 SD below the mean) are defined as having low bone density (osteopenia) and are also at increased risk of osteoporosis. More than 50% of the fractures, including hip fractures, among postmenopausal women occur in this group. Teriparatide is one of the most effective treatment options for osteoporosis. But the cost of teriparatide is prohibitively expensive and in countries like India with limited personal resources of the individuals, its not a feasible option in the majority of the patients with severe osteoporosis. The investigators aim to compare weekly versus daily teriparatide therapy in an open label non inferiority trial and if successful, the investigators anticipate, the cost of treatment could be reduced considerably so that treatment becomes more affordable to a larger number of patients. Also with weekly therapy, number of multiple injections could be brought down.

NCT ID: NCT01750086 Completed - Clinical trials for Postmenopausal Osteoporosis

Acute Effect of Teriparatide With Bisphosphonate or Denosumab on Bone Resorption

Start date: January 2013
Phase: Phase 4
Study type: Interventional

The aim of the study is to assess the relative antiresorptive properties of 2 osteoporosis medications when combined with teriparatide.