Clinical Trials Directory

Trials / Completed

CompletedNCT03472846

MiDeTe - microRNA Levels Under Denosumab and Teriparatide Therapy in Postmenopausal Osteoporosis

MicroRNAs Levels in Women With Postmenopausal Osteoporosis Under Antiresorptive or Osteoanabolic Treatment

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
26 (actual)
Sponsor
Medical University of Vienna · Academic / Other
Sex
Female
Age
60 Years – 80 Years
Healthy volunteers
Accepted

Summary

The aim of this study is the quantitative determination of bone-specific microRNAs in the serum of postmenopausal women with osteoporosis during antiresorptive or osteoanabolic therapy.

Detailed description

Primarily the influence of the therapeutic treatment on the microRNA concentration in the serum (treatment-response) and the relation between microRNA serum levels and changes of the bone mineral density will be investigated. These data will help to examine the use of microRNAs as novel diagnostic biomarkers for the diagnosis of osteoporosis and targeted therapeutic treatment of patients.

Conditions

Interventions

TypeNameDescription
DRUGProlia, 60 Mg/mL Subcutaneous Solutionantiresorptive treatment with Prolia
DRUGTeriparatideosteoanabolic treatment with Forsteo

Timeline

Start date
2017-03-01
Primary completion
2022-09-01
Completion
2022-09-30
First posted
2018-03-21
Last updated
2023-01-26

Locations

1 site across 1 country: Austria

Source: ClinicalTrials.gov record NCT03472846. Inclusion in this directory is not an endorsement.

MiDeTe - microRNA Levels Under Denosumab and Teriparatide Therapy in Postmenopausal Osteoporosis (NCT03472846) · Clinical Trials Directory