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Trial · NCT00926380

Denosumab, Teriparatide or Both for the Treatment of Postmenopausal Osteoporosis

NCT00926380, Phase 2, Completed, Massachusetts General Hospital; results first posted 2018-05-08

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Denosumab, Teriparatide or Both for the Treatment of Postmenopausal Osteoporosis. Trials, record NCT00926380. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00926380

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Denosumab, Teriparatide or Both for the Treatment of Postmenopausal Osteoporosis
NCT number
NCT00926380
Status
Completed
Phases
Phase 2
Enrollment
94 participants, actual
Lead sponsor
Massachusetts General Hospital
Conditions
Osteoporosis
Interventions
denosumab, teriparatide
First posted
2009-06-23
Last updated
2018-06-29
Results first posted
2018-05-08

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange in Spine Bone Density From Baseline to 2 YearsBaseline and 2 years

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange in Spine Bone Density From Baseline to 2 YearsBaseline and 2 yearspercent changeMEAN

Results by group3

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Change in Spine Bone Density From Baseline to 2 YearsDenosumab ONLY8.3Standard Error 3.4percent change
Change in Spine Bone Density From Baseline to 2 YearsTeriparatide (Forteo®) ONLY9.5Standard Error 5.9percent change
Change in Spine Bone Density From Baseline to 2 YearsDenosumab and Teriparatide (Forteo®)12.9Standard Error 5.0percent change

Participant flow18

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Year 1STARTEDDenosumab ONLY33
Year 1STARTEDTeriparatide (Forteo®) ONLY31
Year 1STARTEDDenosumab and Teriparatide (Forteo®)30
Year 1COMPLETEDDenosumab ONLY33
Year 1COMPLETEDTeriparatide (Forteo®) ONLY30
Year 1COMPLETEDDenosumab and Teriparatide (Forteo®)29
Year 1NOT COMPLETEDDenosumab ONLY0
Year 1NOT COMPLETEDTeriparatide (Forteo®) ONLY1
Year 1NOT COMPLETEDDenosumab and Teriparatide (Forteo®)1
Year 2STARTEDDenosumab ONLY33

Adverse events21

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherRashSkin and subcutaneous tissue disordersDenosumab ONLY433
otherRashSkin and subcutaneous tissue disordersTeriparatide (Forteo®) ONLY031
otherRashSkin and subcutaneous tissue disordersDenosumab and Teriparatide (Forteo®)230
otherReactions at injection siteSkin and subcutaneous tissue disordersDenosumab ONLY033
otherReactions at injection siteSkin and subcutaneous tissue disordersTeriparatide (Forteo®) ONLY231
otherReactions at injection siteSkin and subcutaneous tissue disordersDenosumab and Teriparatide (Forteo®)030
otherHypercalcemiaEndocrine disordersDenosumab ONLY033
otherHypercalcemiaEndocrine disordersTeriparatide (Forteo®) ONLY031
otherHypercalcemiaEndocrine disordersDenosumab and Teriparatide (Forteo®)230
otherNauseaGastrointestinal disordersDenosumab ONLY033

Adverse event totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityDenosumab ONLY
Total, all-cause mortalityTeriparatide (Forteo®) ONLY
Total, all-cause mortalityDenosumab and Teriparatide (Forteo®)
Total, other adverse eventsDenosumab ONLY433
Total, other adverse eventsTeriparatide (Forteo®) ONLY531
Total, other adverse eventsDenosumab and Teriparatide (Forteo®)430
Total, serious adverse eventsDenosumab ONLY133
Total, serious adverse eventsTeriparatide (Forteo®) ONLY231
Total, serious adverse eventsDenosumab and Teriparatide (Forteo®)130

Papers14

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
9520411BACKGROUNDPubMed
9568710BACKGROUNDPubMed
11341338BACKGROUNDPubMed
11346808BACKGROUNDPubMed
11564687BACKGROUNDPubMed
14500804BACKGROUNDPubMed
14500805BACKGROUNDPubMed
17164314BACKGROUNDPubMed
18381571BACKGROUNDPubMed
18539106BACKGROUNDPubMed

1 to 10 of 14

See all 14 papers

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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 trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00926380

GET https://conductscience.org/api/trials/v1/NCT00926380/events?page=2