Effects of Genistein Aglycone in Glucocorticoid Induced Osteoporosis
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ClinicalTrials.gov Identifier: NCT03040531 |
Recruitment Status : Unknown
Verified March 2017 by Francesco Squadrito, University of Messina.
Recruitment status was: Recruiting
First Posted : February 2, 2017
Last Update Posted : March 3, 2017
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Osteoporosis, Steroid Induced | Dietary Supplement: Genistein aglycone Drug: Alendronate Oral Tablet Dietary Supplement: Calcium + vitamin D3 tablet | Phase 2 Phase 3 |

Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 200 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Triple (Participant, Care Provider, Investigator) |
Masking Description: | Drugs will be labelled as "A" and "B" and so will be the groups. Patients and doctors involved will not be aware of the treatment. |
Primary Purpose: | Prevention |
Official Title: | Metabolic, Endocrine, and Central Effects of Genistein Aglycone in Glucocorticoid Induced Osteoporosis |
Actual Study Start Date : | January 19, 2017 |
Estimated Primary Completion Date : | June 30, 2018 |
Estimated Study Completion Date : | December 30, 2018 |

Arm | Intervention/treatment |
---|---|
Experimental: Genistein
Each tablet will contain 27 mg of 98% pure genistein + 500mg Calcium + 200 IU Vit. D3. Subjects will receive 2 tablets per day 6 days/week for all the duration of the study. Once a week subjects will receive a tablet containing only 500mg Calcium + 200 IU Vit. D3. |
Dietary Supplement: Genistein aglycone
27mg bid in tablets
Other Name: fosteum |
Active Comparator: Alendronate
Each tablet will contain 500mg Calcium + 200 IU Vit. D3. Subjects will receive 2 tablets per day 6 days/week for all the duration of the study. Once a week subjects will take one tablet containing 70mg alendronate. |
Drug: Alendronate Oral Tablet
70 mg/week in tablets
Other Name: Fosamax Dietary Supplement: Calcium + vitamin D3 tablet 500mg Calcium + 200 IU Vitamin D3 bid in tablets |
- Change in Bone mineral density [ Time Frame: 24 months ]BMD of lumbar spine and femoral will be measured by DEXA (dual energy x-ray absorptiometry)
- Bone fracture [ Time Frame: 24 months ]Xrays of the lumbar spine (T4-L4) will be taken to evaluate the presence of fractures
- Change in Bone quality [ Time Frame: 24 months ]pQCT (peripheral quantitative computed tomography) will be used for bone quality evaluation
- Change in Bone markers [ Time Frame: 24 months ]bone turnover markers will be evaluated on peripheral blood
- Change in Cardiovascular markers [ Time Frame: 24 months ]Markers of cardiovascular risk will be evaluated on peripheral blood
- Change in Glucose and lipid metabolism [ Time Frame: 24 months ]Glycaemia and blood lipids will be evaluated on peripheral blood
- Change in Quality of life [ Time Frame: 24 months ]European Quality of Life Questionnaire will be administered to subjects
- Chage in skin elasticity [ Time Frame: 24 months ]skin elasticity will be tested in subjects taking glucocorticoids
- Change in thyroid markers [ Time Frame: 24 months ]markers of thyroid function will be evaluated on peripheral blood
- Change in inflammatory markers [ Time Frame: 24 months ]markers of inflammation will be evaluated on peripheral blood
- Polymorphisms of estrogen receptor [ Time Frame: 24 months ]Estrogen receptor polymorphisms will be evaluated on white blood cells

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Ages Eligible for Study: | 54 Years to 75 Years (Adult, Older Adult) |
Sexes Eligible for Study: | Female |
Gender Based Eligibility: | Yes |
Gender Eligibility Description: | Only female XX patients will be included, to avoid interactions with other steroid drugs. |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- being treated with glucocorticoids (5 mg of prednisone equivalents) for the preceding 3 months or less, and expect to continue the therapy for at least 12 months;
- being post-menopausal;
Exclusion Criteria:
- use of other steroids or osteoporosis medications;
- have been diagnosed with metabolic bone diseases (other than glucocorticoid osteoporosis)
- previous (1 year) or current use of HRT (hormone replacement therapy)
- other diseases that may affect participation (i.e. mental illness)

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03040531
Contact: Francesco Squadrito, MD | +390902213648 | fsquadrito@unime.it |
Italy | |
University of Messina | Recruiting |
Messina, Italy, 98123 | |
Principal Investigator: Francesco Squadrito, MD | |
University Hospital | Recruiting |
Messina, Italy, 98125 | |
Contact: Francesco Squadrito, MD +390902213648 fsquadrito@unime.it | |
Principal Investigator: Marco Atteritano, MD | |
Sub-Investigator: Alessandra Bitto, MD/PhD |
Study Director: | Francesco Squadrito, MD | University of Messina |
Responsible Party: | Francesco Squadrito, Full Professor of Pharmacology, University of Messina |
ClinicalTrials.gov Identifier: | NCT03040531 |
Other Study ID Numbers: |
45/16 |
First Posted: | February 2, 2017 Key Record Dates |
Last Update Posted: | March 3, 2017 |
Last Verified: | March 2017 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
glucocorticoid genistein alendronate |
Osteoporosis Bone Diseases, Metabolic Bone Diseases Musculoskeletal Diseases Metabolic Diseases Vitamin D Cholecalciferol Alendronate Genistein Calcium Vitamins Micronutrients Nutrients Growth Substances |
Physiological Effects of Drugs Calcium-Regulating Hormones and Agents Bone Density Conservation Agents Anticarcinogenic Agents Protective Agents Antineoplastic Agents Protein Kinase Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Phytoestrogens Estrogens, Non-Steroidal Estrogens Hormones Hormones, Hormone Substitutes, and Hormone Antagonists |