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Bone Resorption clinical trials

View clinical trials related to Bone Resorption.

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NCT ID: NCT01505348 Completed - Bone Resorption Clinical Trials

Effect of Fasting Versus Feeding on the Bone Metabolic Response to Running

Start date: July 2007
Phase: N/A
Study type: Interventional

This study examined changes in bone metabolism (markers of bone turnover, calcium metabolism) with a bout of acute treadmill running preceded by either a single, mixed meal or an overnight fast.

NCT ID: NCT01233557 Completed - Clinical trials for Metastatic Prostate Cancer

Biomarkers of Bone Resorption in Metastatic Prostate Cancer

Start date: September 2010
Phase: N/A
Study type: Observational

Biomarkers of bone resorption will be measured in the blood of patients with bone metastases from prostate cancer during the course of their illness. Changes in these biomarkers will be correlated with the patient's treatment with antiandrogen therapy and bisphosphonates and the response and/or progression of their cancer. It is hoped that serial measurement of these biomarkers may allow therapeutic monitoring in the future with successful individualisation of bisphosphonate therapy for metastatic prostate cancer.

NCT ID: NCT01097499 Not yet recruiting - Analgesia Clinical Trials

Low Level Laser (LED) Use to Increase Dental Implant Stability and Post Operative Analgesia

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

Study hypothesis: Low level laser (LED) will reduce initial bone resorption and improve primary stability of dental implant. It will also reduces post operative pain compared to patient without treatment Implant osseointegration depends on many factors including biocompatibility of implant materials, design, surface, surgical access, patient conditions, biomechanical status, and lack of primary stability. Several in vivo and in vitro studies showed the healing effect of low level laser therapy (LLLT) on bone by decreasing the initial bone resorption postoperatively and increasing the primary stability of the implant. It has also shown to have an analgesic effect intraorally when used post intraoral surgical procedures. The exact mechanism is unclear despite the fact that many hypothesis has been proposed. In our study, our goal is to present, in a randomized standardized clinical trial, the effect of LLLT on post operative implant stability assessed by resonance frequency analysis (RFA). We will assess the subjective measures of postoperative pain using visual analog scale (VAS).

NCT ID: NCT00904423 Terminated - Breast Cancer Clinical Trials

Ph I/II of Vitamin D on Bone Mineral Density & Markers of Bone Resorption

Start date: April 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Aromatase inhibitors are potent suppressors of breast cancer growth, but side effects include bone loss, fractures, arthralgias and myalgias. We hypothesize vitamin D administration might be beneficial in treating these symptoms and to protect bone.

NCT ID: NCT00814866 Completed - Clinical trials for Rheumatoid Arthritis

Bone Resorption, Osteoclastogenesis and Adalimumab

BROCA
Start date: September 2008
Phase: N/A
Study type: Interventional

Osteoclastic bone resorption depends on both the capacity to generate osteoclasts (osteoclastogenesis) and on individual osteoclast activity. The investigators objective is to study the effect of anti-TNF therapy on the number of osteoclast precursors in the peripheral blood of patients with Rheumatoid Arthritis, on in vitro osteoclastogenesis and on osteoclast activity before and during the treatment of patients with Rheumatoid Arthritis with Adalimumab.

NCT ID: NCT00730600 Completed - Osteoporosis Clinical Trials

Effect of THAI Traditional Massage on Bone Markers

Start date: June 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to explore the skeletal effect of Thai traditional massage by examining the changes in biochemical markers of bone turnover immediately after the massage.

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: NCT00315770 Active, not recruiting - Overweight Clinical Trials

Health of Young European Families and Fish Consumption

Start date: January 2004
Phase: Phase 1
Study type: Interventional

This is a controlled, randomized, intervention trial (CRIT) with 20-40 year old overweight individuals (n = 320) across Europe in order to distinguish between biologically active components of seafood, i.e., seafood proteins and n-3 lipids, regarding their effects on risk factors for metabolic syndrome, bone health, and weight management.

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.