Postmenopausal Osteoporosis Clinical Trial
Official title:
Resolution of Hyperparathyroidism With High-dose Vitamin D Improves Osteoporosis in Multi-treated Postmenopausal Women
Verified date | April 2022 |
Source | Hospital Regional 1o de Octubre |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Recently, an increase in the prevalence of hyperparathyroidism and hypovitaminosis D in postmenopause women has been occurring in Mexico and the world. Chronic exposure to the parathyroid hormone (PTH) is catabolic for the bone, worsening the state of osteoporosis. However, it is unclear whether these conditions could significantly improve bone mineral density (BMD). In the present work, it was shown that the resolution of hyperparathyroidism in postmenopausal women improves osteoporosis.
Status | Completed |
Enrollment | 47 |
Est. completion date | February 20, 2022 |
Est. primary completion date | December 29, 2021 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - Acceptance to participate in the study with informed consent. - Postmenopausal osteoporosis or osteopenia. - Primary or secondary hyperparathyroidism. - Insufficiency or deficiency of vitamin D. - Multi-treated postmenopausal osteoporosis. - Postmenopausal osteoporosis without treatment. Exclusion Criteria: - Different osteoporosis aetiology not related to oestrogenic deficiency. - Thyroid pathology. - Previous treatment with vitamin D, thiazide diuretics, lithium, Teriparatide or glucocorticoids. - Known allergies to vitamin D. - Addison's disease, pheochromocytoma, and depressive disorders. |
Country | Name | City | State |
---|---|---|---|
Mexico | Peri-postmenopause and bone metabolism clinic. Regional Hospital October 1st ISSSTE | Mexico City |
Lead Sponsor | Collaborator |
---|---|
Hospital Regional 1o de Octubre | National Polytechnic Institute, Mexico, Universidad Nacional Autonoma de Mexico |
Mexico,
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* Note: There are 23 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of Participants with Remission of Hyperparathyroidism | Clinical remission of hyperparathyroidism was evaluated after treatment. | 4 weeks | |
Primary | Number of Participants with Remission of Hypovitaminosis D | Clinical remission of vitamin D deficiency or insufficiency were evaluated after treatment. | 4 weeks. | |
Primary | Change from baseline hip T score at 4 weeks | Osteoporosis in the hip was determined by a T score greater than -2.5 and osteopenia was determined by a T score between -1 to -2.4. | 4 weeks | |
Primary | Change from baseline lumbar spine T score at 4 weeks | Osteoporosis in the lumbar spine was determined by a T-score greater than -2.5 and osteopenia was determined by a T-score between -1 and -2.4. | 4 weeks | |
Secondary | Change from baseline general T score at 4 weeks | Osteoporosis was determined by a T-score greater than -2.5 either in the hip or in the lumbar spine and osteopenia was determined by a T-score between -1 and -2.4 either in the hip or in the lumbar spine. | 4 weeks |
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