Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:27 AM
Ignite Modification Date:
2025-12-25 @ 4:27 AM
NCT ID:
NCT02731820
Eligibility Criteria:
Inclusion Criteria:
* Postmenopausal women, more than 5 years post menopause
* Osteopenia (T-score \< -1 and \> -2.5)
* Low risk of fracture (FRAX: \< 20 major osteoporotic; \< 3 hip fracture)
Exclusion Criteria:
* Hyperkalemia
* Renal insufficiency
* Nephrolithiasis
* Use of potassium sparing diuretics
* Use of potassium supplements
* Use of therapies influencing bone metabolism (e.g. corticosteroids, thiazide diuretics, aromatase inhibitors, estrogens)
* Use of protonic pump inhibitors
* Current or recent use of bisphosphonates (stopped less than three years prior to the start of the study)
* Gastrointestinal disorders that hamper nutrient absorption;
* Mental or psychiatric disorders that preclude the possibility of correctly adhering to the protocol
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT02731820
Study Brief:
Protocol Section:
NCT02731820