Effect of Alfacalcidol on Muscle Function in Osteoporosis Patients

Sarcopenia Clinical Trial

Official title:

Effect of Alfacalcidol on Muscle Function in Osteoporosis Patients; Double-blinded Randomized Controlled Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06272227
• Other study ID #: 4-2023-0986
• Status: Not yet recruiting
• Phase: Phase 4
• Start date: February 13, 2024
• Est. completion date: September 1, 2025

Study information

• Verified date: February 2024
• Source: Yonsei University
• Contact: Yumie Rhee
• Phone: +82-02-2228-1973
• Email: yumie[@]yuhs.ac
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study aims to investigate the potential improvement in muscle function, compared to the placebo group, through the concurrent administration of denosumab and alfacalcidol over a one-year period in postmenopausal women with functional sarcopenia and osteoporosis aged 65 and older. The study is planned as a double-blinded randomized controlled trial, intending to recruit a total of 340 participants. Primary outcome is the improvement in SPPB score of 0.5 or more compared to the control group.

Description:

This trial is a double-blind, randomized phase 4 trial to evaluate whether alfacalcidol co-administration improves muscle function compared to the placebo group in functional sarcopenia women over 65 years of age who are taking denosumab for osteoporosis. This trial consists of four trial periods (Screening Visit 1, Baseline Visit 2, Visit 3 (26 weeks), and Visit 4 (52 weeks).

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 340
• Est. completion date: September 1, 2025
• Est. primary completion date: September 1, 2025
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 65 Years and older

Eligibility

Inclusion Criteria:

• 1) Females aged 65 and above. 2) Individuals with osteoporosis who are either currently on denosumab or planning to initiate denosumab treatment.

3) Participants committed to a minimum of 1-year denosumab treatment. 4) Those who have not taken any active vitamin D supplements within 3 months prior to the baseline visit (Visit 2).

5) Participants capable of walking. 6-1) Individuals with SPPB = 9 meeting the criteria for low physical performance.

6-2) Individuals with SPPB scores of 10 or 11 and concurrently exhibiting low muscle strength (hand grip strength < 18kg) or gait speed < 1.0 m/s or chair stand test > 11s (sitting position) or a history of fractures (excluding skull, cervical spine, fingers, toes, and rib fractures) or a fall within the past year.

7) Individuals who have undergone DXA (Dual-energy X-ray Absorptiometry) within 6 months of the baseline visit (Visit 2).

8) Participants who, after receiving a detailed explanation of the clinical trial, have fully understood it, voluntarily decided to participate, and provided written consent to participate while agreeing to adhere to the precautions

Exclusion Criteria:

1. Individuals contraindicated for active vitamin D supplementation:

• Patients with hypercalcemia or hyperphosphatemia. ? Those with a history of urolithiasis/nephrolithiasis.

2. Individuals contraindicated for denosumab treatment:

? Those planning or with unresolved invasive dental procedures such as extractions, dental implants, or oral surgery.

• Individuals with hypoalbuminemia-corrected serum calcium outside the normal range.

3. Individuals with vitamin D deficiency, defined as a serum 25(OH)D concentration below 12 ng/mL (30 nmol/L).

4. Participants who have received continuous prednisolone (or equivalent glucocorticoid) at a dose of 5 mg or higher per day for at least 90 days within 6 months of the screening visit (Visit 1).

5. Individuals with severe malnutrition, indicated by a serum albumin level of 3.0 mg/dL or below.

6. Those in an acute immobility state due to reasons such as fracture, hospitalization, or surgery within 1 month of the baseline visit (Visit 2).

7. Individuals with severe underlying conditions:

? Patients with metastatic cancer.

? Those with severe renal impairment (estimated Glomerular Filtration Rate; eGFR) less than 15 mL/min/1.73m² or undergoing dialysis.

? Individuals receiving oxygen therapy due to chronic obstructive pulmonary disease (COPD).

? Those with decompensated liver cirrhosis and severe liver disease with complications due to portal hypertension

8. Individuals with physical limitations due to specific conditions other than muscle decline: ? Those incapable of communication, including severe dementia. ? Individuals undergoing drug therapy for neuro-muscular disorders such as Parkinson's disease or severe myasthenia.

9. Individuals with an SPPB score of 12, indicating no impairment in physical function

Related Conditions & MeSH terms

• Osteoporosis
• Sarcopenia

Intervention

Drug:
• alfacalcidol
Subjects assigned to arm 1 take two doses of alfacalcidol once a day for a total of 52 weeks from the day after baseline visit 2 to the day before the end of the test (visit 4).
• placebo
Subjects assigned to arm 2 take two doses of placebo once a day for a total of 52 weeks from the day after baseline visit 2 to the day before the end of the test (visit 4).
• Denosumab
denosumab

Locations

Country	Name	City	State
Korea, Republic of	Division of Endocrinology, Department of internal Medicine, Yonsei University College of Medicine, Severance Hospital	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Improvement in SPPB score of 0.5 or more compared to the control group	Our study aim is to demonstrate the improvement in SPPB(Short physical performace battery) score of 0.5 or more in the alfacalcidol group compared to the placebo group.	one year