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Clinical Trial Details

Trial ID: L4027
Source ID: NCT03472846
Associated Drug: Prolia, 60 Mg/Ml Subcutaneous Solution
Title: MiDeTe - microRNA Levels Under Denosumab and Teriparatide Therapy in Postmenopausal Osteoporosis
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Postmenopausal Osteoporosis|Diabetes Type 2
Interventions: DRUG: Prolia, 60 Mg/mL Subcutaneous Solution|DRUG: Teriparatide
Outcome Measures: Primary: detection of microRNA concentration in serum, influence of antiresorptive or osteoanabolic Treatment on microRNA levels in postmenopausal women with osteoporosis, 24 months | Secondary: microRNAs and changes in bone metabolism under treatment, correlation of microRNA with bone turnover markers, fracture risk, BMD, 24 months
Sponsor/Collaborators: Sponsor: Medical University of Vienna | Collaborators: St. Vincent Hospital, Vienna
Gender: FEMALE
Age: ADULT, OLDER_ADULT
Phases: PHASE4
Enrollment: 26
Study Type: INTERVENTIONAL
Study Designs: Allocation: NON_RANDOMIZED|Intervention Model: CROSSOVER|Masking: NONE|Primary Purpose: DIAGNOSTIC
Start Date: 2017-03-01
Completion Date: 2022-09-30
Results First Posted:
Last Update Posted: 2023-01-26
Locations: Medical University Vienna; St. Vincent Hospital, Vienna, 1060, Austria
URL: https://clinicaltrials.gov/show/NCT03472846