NCT04905277CompletedPhase 2
Atenolol for the Prevention of Osteoporosis (APO)
Beta1-Selective Blockade for Prevention of Postmenopausal Bone Loss: A Phase 2, Multi-Center, Double-Blinded, Randomized Placebo-Controlled Trial
Source: ClinicalTrials.gov · Last updated 5 May 2026
Brief summary (registry, in English)
Evaluate whether treatment with a widely used beta blocker, atenolol, will prevent bone loss at the lower back and hip in postmenopausal women.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 420 (actual)
- First submitted
- 24 May 2021
- Start date
- 27 Jul 2021
- Primary completion date
- 2 Feb 2026
- Lead sponsor
- Sundeep Khosla, M.D.
- Diseases
- Osteoporosis
- NCT number
- NCT04905277
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 420
- From 27 Jul 2021 to the primary completion date, 2 Feb 2026
- 3 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Undergoing treatment with any medications that affect bone turnover, including the following:
- adrenocorticosteroids (oral for \> 3 months within the past year or year-round use of inhaled corticosteroid use)
- anticonvulsant therapy for seizures (carbamazepine, phenobarbital, or phenytoin within the previous year) pharmacological doses of: thyroid hormone (causing decline of thyroid stimulating hormone below normal, i.e. \< 0.3 miU/L) bisphosphonates (within the past 3 yrs; if taken orally \>1 month in past 3 years) denosumab, romosozumab, estrogen therapy (does not include creams or suppositories) or treatment with a selective estrogen receptor modulator, or teriparatide/abaloparatide (\> 1 month within the past year); aromatase inhibitors (\>1 month within the past year)
- Current use of digitalis glycosides
- Thiazides (\< 6 months of use prior to screening)
- Current or within the past 3 months use of beta blockers
- Any recent fracture within the past 6 months prior to screening (other than fingers, toes and facial fractures, which are all acceptable)
Other illness
- Clinical diagnosis of diabetes mellitus requiring insulin
- Resting systolic blood pressure \< 115 mm Hg, heart rate \< 55 bpm (average of 3 readings after a 5-minute rest and one minute between readings with an automatic cuff)
Lab values
- Clinically significant abnormality in any of the additional screening laboratory studies
- Calcium - \> upper limit lab value per site
- AST- 2x upper normal limit
- eGFR- \< 45 mL/min/1.73m2 based on creatinine
- Presence of (documented clinical diagnosis of any of the following):
- Significant liver or renal disease
- Malignancy (current diagnosis including myeloma or melanoma)
- Radiation (the site PI will determine eligibility on a case-by-case basis)
- Malabsorption (current clinical diagnosis or actively receiving treatment)
- Hypoparathyroidism (current clinical diagnosis or actively receiving treatment)
- Hyperparathyroidism (current clinical diagnosis or actively receiving treatment)
- Acromegaly
- Cushing syndrome
- Hypopituitarism
- Severe chronic obstructive pulmonary disease
- Pheochromocytoma (current clinical diagnosis or actively receiving treatment)
- History of cardiac failure
- Ejection Fraction \<35% (based on most recent EF within the last 12 months, if available)
- PR interval \> 200 msec on screening ECG or known heart block
- History of bronchospastic disease with treatment (asthma, bronchitis)
- Gastric Bypass
- Parkinson's
- Rheumatoid Arthritis
- Psoriatic Arthritis
- Connective Tissue disease
- Patients with serum 25-hydroxyvitamin D levels of \< 20 ng/ml, in order to ensure vitamin D sufficiency
Other
- A1c- ≥8
- FSH- \< 16IU/L
- CBC- Per PI interpretation of each patient
- Bilateral hip replacements or metal in both hips
Who the study is looking for
- Able and willing to provide informed consent
- Postmenopausal women (FSH ≥ 16 IU/L) (no menses for at least one year)
- Aged 50-75 years
Age in the registry: 50 years to 75 years · Sex: Female · Accepts healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Columbia University Irving Medical Center Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Mayo Clinic Coordinator of this site? Confirm its status | Rochester | United States | Unknown status |
| MaineHealth Coordinator of this site? Confirm its status | Scarborough | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.