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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT00957606 Recruiting - Prostate Cancer Clinical Trials

Osteoporosis Among Men Treated With Androgen Deprivation for Prostate Cancer

Osteoporosis
Start date: August 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is - to determine the rate of osteoporosis among patients with advanced prostate cancer. - to propose an algorithm for early detection of patients with advanced prostate cancer who are at risk of developing osteoporosis.

NCT ID: NCT00727493 Recruiting - Osteoporosis Clinical Trials

Osteoporosis and Dental Implant

OPOZAHN
Start date: January 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the influence of alendronate therapy on the wound healing after dental implants in patients with osteoporosis.

NCT ID: NCT00463411 Recruiting - Osteoporosis Clinical Trials

Study of Male Osteoporosis and Aging

Start date: December 2006
Phase: N/A
Study type: Observational

The aim of this study is to identify potential risk factors for fragility fractures in men.

NCT ID: NCT00391404 Recruiting - Osteoporosis Clinical Trials

Fosamax for Childhood Cancer Survivors

Start date: May 2006
Phase: Phase 3
Study type: Interventional

Survivors of childhood cancers face a variety of long-term problems. The investigators' recent study found that osteoporosis and osteopenia were common among these patients. The factors leading to, as well as the best treatment option for, this morbidity are unclear. Bisphosphonates are currently the standard therapy for osteoporosis in the elderly. However, the efficacy and safety of bisphosphonates for treating osteoporosis in long-term cancer survivors have not been tested. The investigators hypothesize that alendronate, an orally active bisphosphonate, is efficacious and safe in the treatment of osteoporosis in these patients.

NCT ID: NCT00346190 Recruiting - Osteoporosis Clinical Trials

The Study of the Early Administration of Alendronate on Prevention of Bone Loss After Hip Fracture.

Start date: January 2003
Phase: Phase 3
Study type: Interventional

To determine whether administration of Alendronate early is more effective than late in the prevention of osteoporosis following a hip fracture

NCT ID: NCT00303784 Recruiting - Prostate Cancer Clinical Trials

Prostate Adenocarcinoma TransCutaneous Hormones

PATCH
Start date: March 2006
Phase: Phase 3
Study type: Interventional

RATIONALE: The increasingly prolonged and extended use of androgen deprivation therapy (ADT) in the treatment of prostate cancer, usually achieved through the administration of LHRH agonists, has raised concerns about long-term toxicities, in particular osteoporosis and adverse metabolic changes which may be associated with type II diabetes and increased cardiovascular risk. An alternative approach is to investigate other methods of ADT. Oral oestrogen has been shown to be as effective as LHRH and surgical orchidectomy in achieving castrate levels of testosterone and has equivalent or improved prostate cancer outcomes but is not used routinely as first-line therapy because of the risk of cardiovascular system (CVS) complications. The CVS complications have been attributed to first-pass hepatic metabolism. Administering oestrogen parenterally avoids the entero-hepatic circulation and so is expected to mitigate the risk of CVS toxicity whilst still effectively suppressing testosterone to castrate levels. This hypothesis has been supported by results from the early stages of this trial which have provided sufficient indication of the safety and efficacy of the patches to warrant further investigation of the treatment in this setting, as recommended by the IDMC.. PURPOSE: This randomized phase III trial is studying how well the estrogen skin patch works compared with luteinizing hormone-releasing hormone agonist injections in treating patients with locally advanced or metastatic prostate cancer.

NCT ID: NCT00202956 Recruiting - Osteoporosis Clinical Trials

Safety and Efficacy Study of Bugusan (BGS)to Treat Osteoporosis.

Start date: June 2004
Phase: Phase 2
Study type: Interventional

The objective is to evaluate the effects on biomarkers and safety of BGS in postmenopausal patients with osteoporosis.

NCT ID: NCT00154609 Recruiting - Osteoporosis Clinical Trials

Davallia Divaricata BL: The Use of Traditional Chinese Native Medicine for Osteoporosis

Start date: January 2002
Phase: Phase 1
Study type: Interventional

We, the investigators at National Taiwan University Hospital, have determined the therapeutic and toxic effects of the traditional herb on the ovariectomized Wistar rat. The final years will determine its effects on the therapy of women who are over 45 years old and postmenopausal with osteoporosis.

NCT ID: NCT00069173 Recruiting - Osteoporosis Clinical Trials

Preventing Osteoporosis in Adolescent Girls

Start date: July 2000
Phase: Phase 1
Study type: Interventional

Physical activity in adolescents is an important part of bone health. Good bone health in adolescents can decrease the risk of osteoporosis. This study will evaluate a program designed to increase the level of physical activity in adolescent girls.