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Parathyroidectomy and Mobility Study

Rescuing Mobility Function Through Surgical Removal of the Parathyroid Gland

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07103876
Enrollment
80
Registered
2025-08-05
Start date
2025-08-15
Completion date
2027-03-31
Last updated
2026-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperparathyroidism, Mobility, Parathyroid

Keywords

Physical Function, Inflammatory Biomarkers, Parathyroidectomy, Aging, Physical activity

Brief summary

This study evaluates whether surgical removal of the parathyroid gland (parathyroidectomy) improves physical function and mobility in older adults with primary hyperparathyroidism (PHPT). PHPT, a common endocrine disorder in older adults, is associated with reduced muscle strength, mobility, and quality of life. This prospective observational study will enroll up to 80 participants aged 60 and older undergoing parathyroidectomy at UF Health. Participants will complete physical performance tests, wear an Actigraph device to assess physical activity, and provide blood samples for biomarker analysis at pre- and post-operative time points. The goal is to characterize changes in physical function and activity following surgery and to identify biomarkers that may predict mobility improvements. Findings will help inform future larger-scale studies and could expand surgical indications for PHPT in older adults.

Interventions

None listed

Sponsors

University of Florida
Lead SponsorOTHER
National Institute on Aging (NIA)
CollaboratorNIH

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
60 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

Inclusion: * Age ≥ 60 years; * Biochemical diagnosis of hypercalcemic (corrected serum calcium \>10.2 mg/dL or ionized serum calcium \>1.31 mmol/dL or 5.2 mg/dL on at least one serum sample) primary hyperparathyroidism as determined by board-certified endocrinologist or endocrine surgeon; * Undergoing parathyroidectomy at UF Health; * Willing and able to give informed consent. Exclusion: * Failure to provide informed consent; * Biochemical diagnosis of eucalcemic primary hyperparathyroidism (corrected serum calcium ≤10.2 mg/dL or ionized serum calcium ≤1.31 mmol/dL or 5.2 mg/dL on at least one serum sample); * Elected not to undergo parathyroidectomy at UF Health; * Major surgery as deemed by principal investigator or hip/knee replacement in the past 6 months; * Fractures to the hands, arms or legs within the last 6 months; * Traumatic accident (i.e. motor vehicle collision, fall from elevation, etc.) resulting in orthopedic trauma or requiring prolonged immobilization (\>2 weeks) within the last 6 months; * Blood transfusion within the past 3 months; * Self-reported myocardial infarction, cerebrovascular accident, or unstable angina within the past 6 months; * NYHA Class 3 or 4 congestive heart failure; * Major psychiatric disorder; * Cancer requiring treatment in the past 1 year (including metastatic cancer), except for locally treated non-melanoma skin cancers or cancers that have clearly been cured or in the opinion of the investigator carry an excellent prognosis (e.g., Stage 1 cervical cancer); * Renal failure requiring hemodialysis or peritoneal dialysis * Use of bone-modifying therapies (alendronate \[Fosamax\], zoledronic acid \[Reclast\], denosumab \[Prolia or Xgeva\], or romosozumab \[Evenity\]) within 1 month of planned surgery * Planning to permanently leave the area within 3 months of parathyroidectomy; * Vision or hearing impairment - defined as unable to read or listen/follow instructions despite the use of maximal assistive devices (i.e. contact lenses, glasses, hearing aids, etc.) * Participating in another clinical trial or has received an investigational product within 30 days prior to screening/enrollment.

Design outcomes

Primary

MeasureTime frameDescription
Distance Walked in Six-Minute Walk Test (6MWT)At pre-operative assessment and at 3 month post-operative assessmentMeasures walking endurance and aerobic capacity by recording the distance walked in six minutes along a 20-meter course.
Short Physical Performance Battery ScoreAt pre-operative assessment and at 3 month post-operative assessmentA composite test assessing balance, gait speed (4-meter walk), and lower body strength (chair stands). Higher scores reflect better function.
Isokinetic Knee Strength (Biodex)At pre-operative assessment and at 3 month post-operative assessmentAssesses lower limb muscle strength and endurance using a dynamometer. Reports peak torque and fatigue index.
Grip StrengthAt pre-operative assessment and at 3 month post-operative assessmentHandgrip strength is measured using a dynamometer as a marker of overall muscle strength and frailty risk.
Intensity of Movement using ActiGraph AccelerometryAt pre-operative assessment and at 3 month post-operative assessmentAn objective measure of free-living physical activity using a wearable hip device that captures intensity of movement over 7 days.
Frequency of Movement using ActiGraph AccelerometryAt pre-operative assessment and at 3 month post-operative assessmentAn objective measure of free-living physical activity using a wearable hip device that captures frequency of movement over 7 days.
Duration of Movement using ActiGraph AccelerometryAt pre-operative assessment and at 3 month post-operative assessmentAn objective measure of free-living physical activity using a wearable hip device that captures duration of movement over 7 days.
CHAMPS Questionnaire ScoreAt pre-operative assessment and at 3 month post-operative assessmentA validated self-report tool for older adults that measures weekly frequency and duration of common physical activities.
Pasieka Parathyroidectomy Assessment of Symptoms (PAS)At pre-operative assessment and at 3 month post-operative assessmentA validated 13-item questionnaire measuring severity of neurocognitive and neuromuscular symptoms common in PHPT, such as fatigue, irritability, and memory loss.
Concentration of Plasma Cytokine BiomarkersBlood work will be collected at the pre-operative assessment, the 2 week post-operative assessment, 3 month post-operative assessment and the 6 month post-operative assessmentBlood-based analysis of myokines (e.g., IL-6, myostatin, LIF, irisin), osteokines (e.g., IGF-1, FGF-21, osteocalcin), and adipokines (e.g., adiponectin, TNF-α) associated with muscle-organ crosstalk, inflammation, and mobility.

Countries

United States

Contacts

CONTACTRezvan Ghaderpanah, MD
ghaderpanah.r@ufl.edu352-273-5919
CONTACTAditya Shirali, MD
aditya.shirali@surgery.ufl.edu352-265-0169

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 16, 2026