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Bone Resorption clinical trials

View clinical trials related to Bone Resorption.

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NCT ID: NCT00558623 Completed - Pregnancy Clinical Trials

Dietary Calcium Supplementation to Reduce Blood Lead in Pregnancy

Start date: January 2001
Phase: N/A
Study type: Interventional

Lead accumulates in bone. During pregnancy, physiologic changes occur prompting bone resorption in order to provide calcium to the growing fetal skeleton also release the lead stored in bone into a pregnant woman's circulation. We have previously demonstrated that lead stores mobilized into the circulation of pregnant women pose a major threat to fetal development. This is particularly unfortunate since bone lead stores, once accumulated, persist for decades, thereby jeopardizing the pregnancies of women even if their current lead exposures have subsided. What then can be done for the many thousands of women who have had lead exposure while growing up and who want to have healthy children? To address this question, in 2000, this project embarked on a randomized intervention trial to test whether a bedtime nutritional supplement of 1,000 mg of calcium can significantly reduce fetal lead exposure and toxicity by suppressing bone resorption in the pregnant mother.

NCT ID: NCT00421408 Completed - Osteoporosis Clinical Trials

The Effect of Protein Supplementation on Bone Health in Healthy Older Men and Women

Start date: February 2007
Phase: Phase 1/Phase 2
Study type: Interventional

Women and men consuming a low protein diet may be at risk for bone loss. The purpose of this study is to determine whether a daily protein supplement will improve bone health among healthy older adults.

NCT ID: NCT00297830 Completed - Clinical trials for Liver Transplantation

Zoledronic Acid Versus Alendronate for Prevention of Bone Loss After Organ Transplantation

CTX
Start date: November 2005
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to compare the effectiveness and safety of zoledronic acid with alendronate in the prevention of bone loss after organ transplantation. Zoledronic acid is given as a single intravenous infusion. Alendronate is given as a weekly pill. Both are expected to be very effective, but it is not known which one will work best.

NCT ID: NCT00264082 Completed - Breast Cancer Clinical Trials

Assessment of Tartrate-Resistant Acid Phosphatase (TRAP) as a Bone Resorption Marker in Stage IV Breast Cancer Patients With Bone Metastasis

Start date: September 2004
Phase: N/A
Study type: Observational

The purpose of this research study is to evaluate the usefulness of the TRAP protein as (1) an early indicator of bone destruction and (2) a tool for assessing the effect of Zometa® in treating symptoms of bone metastases due to breast cancer. Tartrate-resistant acid phosphatase (TRAP) is a protein released into the blood stream as a result of bone destruction caused by metastasis of breast cancer to the bone. Bone destruction causes pain and bone fractures. This study will measure TRAP levels in serum taken from breast cancer patients to see if TRAP levels will be able to predict the effect of Zometa® treatment on bone destruction, pain and bone fractures.

NCT ID: NCT00172055 Completed - Cancer Prostate Clinical Trials

Study to Assess Efficacy and Safety of Zoledronic Acid and the Value of Markers of Bone Resorption in the Prediction of Bone Metastases and Cancer Treatment-induced Bone Loss (CTIBL) in Patients With Prostate Cancer on Hormone Therapy

Start date: December 2004
Phase: Phase 3
Study type: Interventional

The objective of the study is to investigate whether blood markers can be used to predict the development of bone metastases and to assess the efficacy and safety of zoledronic acid in cancer treatment induced bone loss.