Stress Urinary Incontinence and Sarcopenia in Postmenopausal Osteoporosis
Recruiting
Observational Study
Osteoporosis, Postmenopausal
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 50 – 75
- Sex
- Female
- Study type
- Observational
- Participants needed
- 100 (estimated)
- Sponsor
- Beylikduzu State Hospital · Other
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About This Trial
The primary aim of our study is to evaluate the presence of stress urinary incontinence in postmenopausal patients with and without osteoporosis, determine its impact on quality of life, and explore its relationship with sarcopenia.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Postmenopausal women with DXA measurements performed within the last 6 months.
* Based on DXA measurements:
Femoral neck and L1-L4 T-scores of -1 and above will be included in the control group (non-osteoporotic).
Femoral neck and L1-L4 T-scores of -2.5 and below will be inc…
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