Clinical Trials Directory

Trials / Completed

CompletedNCT00074711

Adding Phosphorus to Osteoporosis Drug Treatment

Bone Sparing by Calcium Salts With and Without Extra Phosphorus

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
241 (actual)
Sponsor
Creighton University · Academic / Other
Sex
Female
Age
60 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Osteoporosis causes bones to weaken and break more easily. Calcium and phosphorus are two minerals that are essential for normal bone formation. Unfortunately, calcium salts commonly prescribed in anti-osteoporosis treatment bind phosphorus from food and restrict phosphorus available for bone building. Teriparatide is a drug that reduces the risk of fractures by increasing bone thickness and strength. Vitamin D is also necessary for strong bones and teeth. The purpose of this study is to evaluate the bone-building effectiveness of two calcium supplements, one with a source of phosphorus and one without, in combination with teriparatide and vitamin D in women with osteoporosis.

Detailed description

Osteoporosis is the most common type of bone disease. Calcium supplements normally used in anti-osteoporosis treatment are calcium salts of carbonate or citrate; however, these salts bind phosphorus from food in the intestine and restrict phosphorus available for bone building. This study will evaluate the efficacy of adding calcium phosphate to a regimen of teriparatide and vitamin D in increasing bone mineral density in women with osteoporosis. It is hypothesized that the group taking the phosphate-containing calcium supplement will have greater gains in bone mineral density (BMD) during the course of the study than the group not receiving phosphate. All participants will receive teriparatide and vitamin D during the course of the 12-month study. Participants will be randomly assigned to one of two groups. One group will receive calcium phosphate and the other will receive calcium carbonate. BMD will be measured at spine and hip at baseline and at 3, 6, and 12 months of treatment.

Conditions

Interventions

TypeNameDescription
DRUGCalcium carbonateParticipants will receive teriparatide and vitamin D during the course of the 12-month study. They will also receive calcium carbonate.
DRUGCalcium PhosphateParticipants will receive teriparatide and vitamin D during the course of the 12-month study. They will also receive calcium phosphate.

Timeline

Start date
2004-08-01
Primary completion
2008-06-01
Completion
2008-06-01
First posted
2003-12-22
Last updated
2016-07-06
Results posted
2016-07-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00074711. Inclusion in this directory is not an endorsement.