Actively Recruiting

Age: 60Years - 100Years
All Genders
ID07103876

Rescuing Mobility Function Through Surgical Removal of the Parathyroid Gland

Led by University of Florida · Updated on 2025-09-29

80

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

Sponsors

U

University of Florida

Lead Sponsor

N

National Institute on Aging (NIA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating whether surgical removal of the parathyroid gland (parathyroidectomy) improves physical function and mobility in older adults aged 60 and above with primary hyperparathyroidism (PHPT). PHPT is a common endocrine disorder in older adults that is linked to lower muscle strength, reduced mobility, and poorer quality of life. This prospective observational study aims to better understand changes in physical function and activity after surgery and to identify biomarkers that could predict improvements in mobility. Participants in this study are adults aged 60 or older undergoing parathyroidectomy at UF Health. The study involves physical performance tests, wearing an Actigraph device to monitor physical activity, and providing blood samples for biomarker analysis. These assessments occur before surgery, and at 2 weeks, 3 months, and 6 months post-operation. The goal is to collect detailed data on physical function and biological markers over time. During the study, participants will complete a series of tests including the six-minute walk test, strength measurements, physical activity monitoring, and symptom questionnaires at pre-operative and 3-month post-operative visits. Blood samples are collected at four time points to measure plasma cytokine biomarkers. Researchers will monitor physical activity intensity, frequency, and duration using wearable devices. The total involvement spans several months with multiple assessments to track changes following surgery and safety monitoring throughout.

CONDITIONS

Brief Title

Parathyroidectomy and Mobility Study

Who Can Participate

Age: 60Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 60 years or older
  • Biochemical diagnosis of hypercalcemic primary hyperparathyroidism confirmed by a specialist
  • Scheduled to undergo parathyroidectomy at UF Health
  • Willing and able to give informed consent
Not Eligible

You will not qualify if you...

  • Unable or unwilling to provide informed consent
  • Diagnosis of eucalcemic primary hyperparathyroidism
  • Choosing not to have parathyroidectomy at UF Health
  • Major surgery, hip/knee replacement, or limb fractures within past 6 months
  • Recent traumatic accident causing immobilization within past 6 months
  • Blood transfusion within past 3 months
  • Recent heart attack, stroke, or unstable angina within past 6 months
  • Severe congestive heart failure (NYHA Class 3 or 4)
  • Major psychiatric disorders
  • Cancer treatment within past year except certain cured or low-risk cancers
  • Kidney failure requiring dialysis
  • Use of bone-modifying therapies within 1 month before surgery
  • Planning to permanently leave the area within 3 months after surgery
  • Significant vision or hearing impairment despite assistive devices
  • Participation in another clinical trial or investigational product use within 30 days before screening

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Up to 2 weeks or until discharge.

Participants undergo parathyroidectomy surgery and immediate recovery at UF Health.

1 surgery visit and 1 to 2 post-operative visits

Post-operative Follow-up

Duration - Up to 6 months

Participants are assessed for recovery and mobility function after surgery.

Visits at 2 weeks, 3 months, and 6 months post-operative assessments

Trial Site Locations

Total: 1 location

1

Clinical and Translational Research Building

Gainesville, Florida, United States, 32610

Actively Recruiting

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Research Team

N

Nevena Stanojevic, Bachelor of Science

A

Aditya Shirali, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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