Roles of microRNAs in the Development of Osteoporosis in Men - Preliminary Study
NCT ID: NCT02705040
Last Updated: 2016-03-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
30 participants
OBSERVATIONAL
2013-12-31
2016-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Circulating miRNA in Primary Hyperparathyroidism
NCT03931109
Development of Intervention Model for Osteoporosis and Fall Prevention in Taiwan
NCT01206491
Fracture and Fall Prevention in Elderly With Osteoporosis
NCT01844154
Study on the microRNA Expression Level in Postmenopausal Osteoporosis
NCT02128009
Vitamin D Status and Multi-Omics Profiles in Primary Osteoporosis
NCT07296471
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Normal
bone mineral density T\>=-1.0
Osteopenia
bone mineral density -1.0\>T\>=-2.5
Osteoporosis
bone mineral density T\<-2.5
Osteopenia
bone mineral density -1.0\>T\>=-2.5
Normal
bone mineral density T\>=-1.0
Osteoporosis
bone mineral density T\<-2.5
Osteoporosis
bone mineral density T\<-2.5
Normal
bone mineral density T\>=-1.0
Osteopenia
bone mineral density -1.0\>T\>=-2.5
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Normal
bone mineral density T\>=-1.0
Osteopenia
bone mineral density -1.0\>T\>=-2.5
Osteoporosis
bone mineral density T\<-2.5
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Candidates have no clinical evidence or history of focal lesions of the femur; previous hip surgery or irradiation; hip trauma; spinal trauma.
3. Participants who have thoroughly understood and signed the consent form.
4. Ten normal adult male (age range, 20-40 years).
Exclusion Criteria
2. Participants with Paget's disease, serious liver disease, serious renal disease (indicated by a serum creatinine concentration of more than 1.6mg/dL).
3. Participants who currently or have history of using steroids or hormone replacement therapy.
4. Participants who fail to sign to the consent form.
70 Years
90 Years
MALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Taipei Medical University WanFang Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Ruei-Ming Chen, PhD
Role: PRINCIPAL_INVESTIGATOR
Taipei Medical University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Taipei Medical University Wanfang Hospital
Taipei, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
TMU-JIRB 201310015
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.