MITO: Muscle Impact of Treating Osteoporosis

Sponsor
Nami Safai Haeri (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05666310
Collaborator
The Claude D. Pepper Older Americans Independence Centers (Other), National Institute on Aging (NIA) (NIH)
40
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2
18.9
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Study Details

Study Description

Brief Summary

Osteosarcopenia is a geriatric musculoskeletal syndrome characterized by co-existence of osteoporosis and sarcopenia (low skeletal muscle mass, strength, and/or functional capacity). There is strong evidence of overlap between the pathophysiology of osteoporosis and sarcopenia (muscle-bone crosstalk). This research plan will further explore the relationship between bone and muscle, and provide new information about effect of osteoporosis medications on muscle health in older adults who are under treatment for osteoporosis.

Condition or Disease Intervention/Treatment Phase
  • Drug: Denosumab
  • Drug: Zoledronic Acid
  • Other: Denosumab Placebo
  • Other: Zoledronic Acid Placebo
Phase 4

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
The Impact of Osteoporosis Medications on Muscle Health in Older Adults
Anticipated Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Jul 30, 2024
Anticipated Study Completion Date :
Jul 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Zoledronic Acid

Drug: Zoledronic Acid
Twenty participants will randomly receive zoledronic acid 5 mg intravenous infusion at month 0 with denosumab placebo at month 0 and 6. All forty participants will receive zoledronic acid 5 mg intravenous infusion at month 12.

Other: Denosumab Placebo
Twenty participants who will randomly receive zoledronic acid 5 mg intravenous infusion at month 0 will also receive denosumab placebo at month 0 and 6.

Active Comparator: Denosumab

Drug: Denosumab
Twenty participants will randomly receive denosumab 60 mg subcutaneous injection at month 0 and 6 with zoledronic acid placebo at month 0.

Other: Zoledronic Acid Placebo
Twenty participants who will randomly receive denosumab 60 mg subcutaneous injection at month 0 and 6 will also receive zoledronic acid placebo.

Outcome Measures

Primary Outcome Measures

  1. Percentage change from baseline in muscle mass (kg) measured by D3-Creatine [Baseline vs Month 12]

    D3-Creatine dilution method is a novel method to measure muscle mass

  2. Percentage change from baseline in appendicular lean mass (ALM/body mass index) [Baseline vs Month 12]

    Appendicular lean mass is measured by whole body DXA scan and is an index of skeletal muscle mass

  3. Percentage change from baseline in trabecular bone score (TBS) [Baseline vs Month 12]

    TBS is measure of bone microarchitecture and is measured by a DXA system. A value of ≥ 1.35 indicates a normal architecture while TBS ≤ 1.20 indicates degraded microarchitecture

  4. Percentage change from baseline in bone mineral density (BMD) (g/cm²) [Baseline vs Month 12]

    BMD is measured by a DXA scan system and a higher BMD is correlated with lower fracture risk

  5. Percentage change from baseline in grip strength (kgf) [Baseline vs Month 12]

    Grip strength is measure of muscle strength and will be measured by a standard hand dynamometer

  6. Percentage change from baseline in gait speed (m/s) [Baseline vs Month 12]

    Gait speed is a measure of muscle function and will be measured by standard 4 meter gait speed test

  7. Percentage change from baseline in rectus femoris muscle thickness (cm) [Baseline vs Month 12]

    This variable will be measured by ultrasound

  8. Percentage change from baseline in rectus femoris muscle cross-sectional surface area (cm²) [Baseline vs Month 12]

    This variable will be measured by ultrasound

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Ambulatory adults age ≥65 years including those using assistive devices to maximize generalizability, if they have criteria for treating osteoporosis including:

  1. Osteoporosis by axial bone density (spine, hip or forearm BMD T-score ≤-2.5 SD) or

  2. A previous adult fragility fracture of the spine or hip or

  3. Would be treated based on FRAX National Osteoporosis Foundation treatment thresholds of a 10-year risk of ≥ 20% for a major osteoporotic fracture or ≥ 3% for hip fracture using femoral neck BMD.

Exclusion Criteria:
  1. Patients with a calculated creatinine clearance < 35 ml/min or

  2. Who have a contraindication for bisphosphonates or denosumab or

  3. Those who are scheduled for a tooth extraction to avoid jaw osteonecrosis or

  4. Subjects with severe liver disease or

  5. Those who have been on oral bisphosphonates for the past 1 year and intravenous bisphosphonates for the past 2 years prior to the study or

  6. Men

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Pittsburgh Pittsburgh Pennsylvania United States 15213

Sponsors and Collaborators

  • Nami Safai Haeri
  • The Claude D. Pepper Older Americans Independence Centers
  • National Institute on Aging (NIA)

Investigators

  • Principal Investigator: Nami Safai Haeri, MD, University of Pittsburgh

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nami Safai Haeri, Assistant Professor, University of Pittsburgh
ClinicalTrials.gov Identifier:
NCT05666310
Other Study ID Numbers:
  • STUDY22080139
  • P30AG024827
First Posted:
Dec 27, 2022
Last Update Posted:
Dec 28, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 28, 2022