Trial · NCT00051558
Registered outcomes15
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 15 of 15
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change From Baseline at 18 Month Endpoint in Lumbar Spine Bone Mineral Density (BMD) | 18 month endpoint | change from baseline at endpoint in bone mineral density of the lumbar spine as assessed by dual energy X-ray absorptiometry (DXA) |
| Secondary | Change From Baseline at 18 Month Endpoint in Lumbar Spine Bone Mineral Density (BMD), Female Subset | 18 month endpoint | change from baseline at endpoint in bone mineral density of the lumbar spine as assessed by dual energy X-ray absorptiometry (DXA) |
| Secondary | Time Course of Change From Baseline in Lumbar Spine Bone Mineral Density (BMD), Women and Men Combined | 3, 6, 12, 18, 24, 36 months | change from baseline in bone mineral density of the lumbar spine as assessed by dual energy X-ray absorptiometry (DXA) |
| Secondary | Time Course of Change From Baseline in Lumbar Spine Bone Mineral Density (BMD), Female Subset | 3, 6, 12, and 18 months | change from baseline in bone mineral density of the lumbar spine as assessed by dual energy X-ray absorptiometry (DXA) |
| Secondary | Change From Baseline in Lumbar Spine Bone Mineral Density (BMD), Women and Men Combined | 24 and 36 months and Endpoint at 36 months | change from baseline in bone mineral density of the lumbar spine as assessed by dual energy X-ray absorptiometry (DXA) |
| Secondary | Change From Baseline in Femoral Neck Bone Mineral Density (BMD), Women and Men Combined | 18, 24, 36 months, and 18 and 36 month endpoints | change from baseline in bone mineral density of the femoral neck as assessed by dual energy X-ray absorptiometry (DXA) |
| Secondary | Change From Baseline in Total Hip Bone Mineral Density (BMD), Women and Men Combined | 18, 24, 36 months, and 18 and 36 month endpoints | change from baseline in bone mineral density of the total hip as assessed by dual energy X-ray absorptiometry (DXA) |
| Secondary | Time Course of Change From Baseline in Femoral Neck Bone Mineral Density (BMD), Women and Men Combined | 12, 18, 24, and 36 months | change from baseline in bone mineral density of the femoral neck as assessed by dual energy X-ray absorptiometry (DXA) |
| Secondary | Time Course of Change From Baseline in Total Hip Bone Mineral Density (BMD), Women and Men Combined | 12, 18, 24, and 36 months | change from baseline in bone mineral density of the total hip as assessed by dual energy X-ray absorptiometry (DXA) |
| Secondary | Time Course of Change From Baseline in Bone Turnover Markers in Subset of Patients - Serum N-terminal Propeptide of Type 1 Procollagen | 1, 6, 18, and 36 months | |
| Secondary | Time Course of Change From Baseline in Bone Turnover Markers in Subset of Patients - Serum C-terminal Propeptide of Type 1 Procollagen | 1, 6, 18, and 36 months | |
| Secondary | Time Course of Change From Baseline in Bone Turnover Markers in Subset of Patients - Bone-Specific Alkaline Phosphatase | 1, 6, 18, and 36 months | |
| Secondary | Time Course of Change From Baseline in Bone Turnover Markers in Subset of Patients - Serum Type 1 Collagen Degradation Fragments | 1, 6, 18, and 36 months | |
| Secondary | Time Course of Change From Baseline in Bone Turnover Markers in Subset of Patients - Osteocalcin | 1, 6, 18, and 36 months | |
| Secondary | Any Fracture, Nonvertebral Fractures, Vertebral Fractures, Clinical Vertebral Fractures, and Severity Fractures | 36 months | Clinical vertebral fracture was defined as a radiographically confirmed fracture that was associated with symptoms such as back pain. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT00051558/registered