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Osteoporosis, Postmenopausal clinical trials

View clinical trials related to Osteoporosis, Postmenopausal.

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NCT ID: NCT01709110 Completed - Clinical trials for Postmenopausal Osteoporosis

VERtebral Fracture Treatment Comparisons in Osteoporotic Women

VERO
Start date: October 2012
Phase: Phase 4
Study type: Interventional

The primary purpose of participation in this study is to answer whether teriparatide is superior to risedronate in reducing the occurrence of new vertebral fractures during 24 months of therapy.

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: 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: NCT01657162 Completed - Clinical trials for Postmenopausal Osteoporosis

Twenty-Four Month Extension Study of BA058-05-003 (Abaloparatide) in Participants With Osteoporosis

ACTIVExtend
Start date: November 20, 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to provide 24 months of standard of care data on participants previously enrolled in Study BA058-05-003 (NCT02653417).

NCT ID: NCT01653275 Completed - Osteoporosis Clinical Trials

Mediterranean Diet for Post-menopausal Women: Effects on Bone Turnover

MedSD
Start date: April 2012
Phase: N/A
Study type: Interventional

The investigators propose a 24 week clinical research trial (12 week observational period followed by 12 week MedSD intervention) with feasibility of diet adoption and markers of bone turnover as the primary outcomes.

NCT ID: NCT01652690 Completed - Clinical trials for Osteoporosis, Postmenopausal

Prospective Observational Study to Describe Characteristics and Management of Patients Treated With Denosumab (Prolia®) in Routine Clinical Practice

Start date: June 26, 2012
Phase:
Study type: Observational

The objective of this prospective, observational study in Czech Republic and Slovakia is to describe per country the characteristics of women treated with denosumab in routine clinical practice and the clinical management of these patients during the first 2 years of treatment. In addition, the study aims to collect safety data in the real-life clinical practice settings on adverse drug reactions (ADRs) and serious ADRs.

NCT ID: NCT01575834 Completed - Clinical trials for Postmenopausal Osteoporosis

Efficacy and Safety of Romosozumab Treatment in Postmenopausal Women With Osteoporosis

FRAME
Start date: March 15, 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if treatment with romosozumab is effective in preventing fractures in women with postmenopausal osteoporosis

NCT ID: NCT01572545 Completed - Clinical trials for Postmenopausal Osteoporosis

Comparative Effect of Zoledronic Acid Versus Denosumab on Serum Sclerostin of Postmenopausal Women With Low Bone Mass

DenoZol
Start date: April 2012
Phase: N/A
Study type: Interventional

The primary aim of the study is the comparative effect of zolendronic acid versus denosumab on serum sclerostin levels in postmenopausal women with low bone mass. Secondary aims are their comparative effect on serum dickkopf-1, osteoprotegerin, receptor activator of nuclear factor kappaB ligand (RANKL) and bone turnover markers (procollagen type I N-terminal peptide [PINP] and C-terminal cross-linking telopeptide of type I collagen [CTX]).

NCT ID: NCT01571843 Completed - Clinical trials for Osteoporosis, Postmenopausal

Radius Loading in Primary Hyperparathyroidism

Start date: February 2010
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the effect of forearm exercise on forearm bone density in post-menopausal women with or without primary hyperparathyroidism. The investigators hypothesize that forearm exercise will increase forearm bone density in patients with primary hyperparathyroidism more so than in patients without primary hyperparathyroidism.

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.