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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT00165607 Completed - Osteoporosis Clinical Trials

Randomized, Open, Parallel, Active Controlled Study on Fracture Prevention in Antiosteoporosis Treatment (OF Study)

Start date: April 1996
Phase: Phase 4
Study type: Interventional

To investigate a new incidence and preventive effect of menatetrenone on vertebral fracture in patients with osteoporosis who were randomly assigned to either treatment arm receiving daily dose of calcium supplement as a monotherapy (calcium monotherapy group) or menatetrenone plus calcium supplement as a combination therapy (menatetrenone combo therapy group) for 36 months, followed by a 12-month follow-up observation to examine the preventive effect on the fracture risk.

NCT ID: NCT00163137 Completed - Osteoporosis Clinical Trials

Comparison of Raloxifene and Lasofoxifene - A Randomized, Blinded Study of These Drugs and Placebo on Bone Loss

CORAL
Start date: May 2003
Phase: Phase 3
Study type: Interventional

To compare the effects of 2 years of lasofoxifene treatment with 2 years of raloxifene 60 mg/day use and 2 years of placebo use on bone mineral density (BMD) of the lumbar spine.

NCT ID: NCT00159419 Completed - Osteoporosis Clinical Trials

Bisphosphonate Therapy for Osteogenesis Imperfecta

Start date: August 1999
Phase: Phase 4
Study type: Interventional

The study is designed to evaluate the efficacy and safety of "Bisphosphonate Therapy for Osteogenesis Imperfecta (OI)." We, the researchers at Indiana University School of Medicine, are characterizing the changes effected by oral bisphosphonate therapy and comparing them to a regimen of intravenous bisphosphonate therapy in a group of children with OI and also in children with other disorders that result in low bone mass and fractures.

NCT ID: NCT00157690 Completed - Cystic Fibrosis Clinical Trials

Study of Alendronate to Prevent and Treat Osteoporosis in Cystic Fibrosis Patients

Start date: December 2003
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to determine efficacy of 70 mg alendronate once weekly compared to placebo. This will be measured by percent changes in lumbar spine(LS) bone mineral density(BMD) in adult cystic fibrosis(CF)patients after one year of treatment. The investigators hypothesize that in adult CF patients with osteopenia or osteoporosis, alendronate 70 mg once weekly will produce a mean increase from baseline in lumbar spine BMD that is greater than that observed with placebo at 12 months.

NCT ID: NCT00155675 Completed - Osteoporosis Clinical Trials

Pseudodrynaria Coronana (Wall) Ching

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

The Study to evaluate the clinical effect of "Gusuibu" lasts for 3 years. It aims to evaluate its effect on bone density of postmenopausal osteoporosis. Besides, its effects on the liver, kidney and the hematological influence will be evaluated, too.

NCT ID: NCT00152321 Completed - Osteoporosis Clinical Trials

Strategies Targeting Osteoporosis to Prevent Recurrent Fractures

Start date: September 2003
Phase: N/A
Study type: Interventional

An evidence-based quality improvement intervention will overcome multiple barriers to best practice and improve rates of diagnosis and effective treatment for osteoporosis in high-risk patients. The intervention will be directed at patients (education and counseling) and their primary care physicians (reminders and opinion leader generated and endorsed single page guidelines)

NCT ID: NCT00150969 Completed - Clinical trials for Post-Menopausal Osteoporosis

Vitamin K Supplementation in Post-Menopausal Osteopenia

Start date: January 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether supplementation with 5 mg vitamin K daily over a 2-year period will prevent bone loss in post-menopausal women with osteopenia.

NCT ID: NCT00150696 Completed - Clinical trials for Acute Spinal Cord Injury.

Risedronate for the Prevention of Osteoporosis in People With Spinal Cord Injury.

Start date: February 2000
Phase: Phase 3
Study type: Interventional

The purpose of this study is to find out if Risedronate works to prevent osteoporosis after spinal cord injury.

NCT ID: NCT00150683 Completed - Spinal Cord Injury. Clinical Trials

Effectiveness of Vibration and Standing Versus Standing Alone for the Treatment of Osteoporosis for People With Spinal Cord Injury.

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

The purpose of this study is to find out if standing and/or standing with vibration works for the treatment of osteoporosis for people with a spinal cord injury.

NCT ID: NCT00148915 Completed - Osteoporosis Clinical Trials

A Study To Assess the Quality and Strength of Bone in Women Participants With Osteoporosis Taking Oral Ibandronate Versus Placebo

Start date: August 2005
Phase: Phase 4
Study type: Interventional

The purpose of this randomized, double-blind, placebo-controlled study is to estimate the effect of oral ibandronate sodium (Boniva) taken once monthly versus placebo on bone quality and strength at the proximal femur at one year.