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Osteopenia clinical trials

View clinical trials related to Osteopenia.

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NCT ID: NCT05317013 Terminated - Osteopenia Clinical Trials

CBD in Postmenopausal Women With Osteopenia

Start date: May 1, 2022
Phase: Phase 1
Study type: Interventional

This is a Phase 1, double-blind, placebo-controlled, repeated-dose study to assess the safety, tolerability, and preliminary effects of CHI-554 in postmenopausal women ages 50-80 years who have osteopenia.

NCT ID: NCT01928082 Terminated - Osteoporosis Clinical Trials

The Effects of Estrogen Replacement Therapy in Postmenopausal Women With Hypercalciuria and Low Bone Mass

Start date: August 1, 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess if estrogen replacement normalizes urinary calcium excretion in postmenopausal women with hypercalciuria and low bone mass and to assess for differences in response to estrogen replacement in women with familial hypercalciuria compared to nonfamilial hypercalciuria.

NCT ID: NCT01902186 Terminated - HIV Infection Clinical Trials

Bone Mineral Density Changes in HIV-positive Females With Osteopenia Switching to Raltegravir

RALBAT
Start date: September 2014
Phase: Phase 4
Study type: Interventional

Given the high prevalence of bone alteration in the course of HIV infection or antiretroviral treatment and the favourable properties of raltegravir the investigators designed this pilot randomized and controlled study. Adult female HIV-positive patients on successful treatment with tenofovir/emtricitabine plus atazanavir plus ritonavir will be randomized either to continue such a regimen or to switch to raltegravir plus atazanavir plus ritonavir. Bone mineral density changes will be compared in the two groups at 48 weeks: the hypothesis is that removing tenofovir and using tenofovir will increase bone mineral density at 48 weeks.

NCT ID: NCT01530477 Terminated - Osteopenia Clinical Trials

DXA Precision and Accuracy Comparison Study

DXA P&A
Start date: January 2012
Phase: N/A
Study type: Observational

This study is being conducted to examine the performance of three common DXA machines (1) Lunar iDXA, (2) Lunar Prodigy and (3) Hologic Discovery A in measuring bone density and body fat.

NCT ID: NCT01460654 Terminated - Osteoporosis Clinical Trials

Testosterone and Alendronate in Hypogonadal Men

Start date: October 2011
Phase: Phase 2
Study type: Interventional

This study will investigate the hypothesis that the combination of testosterone replacement and alendronate will improve bone density and parameters of bone quality more than either medication alone in older men with low testosterone levels and low bone density.

NCT ID: NCT01294397 Terminated - Clinical trials for Rheumatoid Arthritis

Effects of Denosumab on the Pharmacokinetics of Etanercept

Start date: March 2011
Phase: Phase 1
Study type: Interventional

This is a multi-center, open-label, single sequence, denosumab single-dose study in postmenopausal women with low bone mineral density (BMD) and rheumatoid arthritis (RA) being treated with etanercept.

NCT ID: NCT00888017 Terminated - Prematurity Clinical Trials

Proton Pump Inhibitor Therapy and Bone Density in Premature Infants

PPI
Start date: April 2009
Phase: N/A
Study type: Observational

Previous research studies have shown that there may be a connection between proton pump inhibitor therapies and hip fracture in adults(1). Proton pump inhibitor(PPI) reflux medications raise the pH of the stomach, which may effect the body's ability to absorb certain calcium compounds. Neonates are at a crucial age for bone mineralization. Because esophageal reflux is common in neonates, PPI therapy is commonly used, despite little information on effectiveness and side effects. PPIs work by blocking the production of protons in the pumps in the stomach, thus making the stomach less acidic. The calcium ion needs an acidic environment in order to be broken down from its natural compounds into an absorbable form (2). This is troubling because of the problems associated with osteopenia in neonates. Bone mineralization is important for premature infants. Rickets and bone fractures are higher in preterm infants than term infants. For this reason, we are investigating whether there is a connection between PPI therapies (specifically Prevacid) and decreased bone densities in neonates. The objective is to determine if a connection exists between proton pump inhibitor antacids and decreased rate of bone mineralization in neonates.

NCT ID: NCT00145704 Terminated - Osteopenia Clinical Trials

Study of Adults With Low Growth Hormone Who Survived Childhood Cancer Where Treatment Caused Low Bone Density

Start date: June 2002
Phase: N/A
Study type: Interventional

The purpose of this project is to evaluate the hypothesis that bisphosphonate treatment given to growth hormone deficient patients (regardless of current growth hormone replacement therapy status and without changing that status) significantly increases total body bone mineral density during an eighteen month period of treatment combined with calcium and Vitamin D when compared to calcium and Vitamin D treatment alone.

NCT ID: NCT00000430 Terminated - Osteoporosis Clinical Trials

Low-Dose Hormone Replacement Therapy and Alendronate for Osteoporosis

Start date: October 1999
Phase: Phase 3
Study type: Interventional

Osteoporosis, a condition in which bones are fragile and break easily, is a major health problem for postmenopausal women. Research studies have shown that both estrogen/progestin replacement therapy (hormone replacement therapy, or HRT) and alendronate are effective in preventing and treating osteoporosis. However, because these drugs work in somewhat different ways, a combination of the two drugs might protect women from osteoporosis better than either drug alone. In this study we will test whether HRT and alendronate given together for 3.5 years to postmenopausal women with low bone mass will have a greater effect on bone than either HRT or alendronate given alone. We will also give every participant in this study calcium and vitamin D supplements.