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Clinical Trials/NCT06562881
NCT06562881
Recruiting
Not Applicable

Patient Navigation to Improve Surgical Access in Primary Hyperparathyroidism

University of Pennsylvania2 sites in 1 country76 target enrollmentFebruary 1, 2026

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hyperparathyroidism, Primary
Sponsor
University of Pennsylvania
Enrollment
76
Locations
2
Primary Endpoint
Parathyroidectomy Surgical Outcome
Status
Recruiting
Last Updated
3 months ago

Overview

Brief Summary

The goal of this study is to address surgical health equity in historically marginalized participants with primary hyperparathyroidism (PHPT). The main questions that this study aims to answer are, how does patient navigation impact:

  • The proportion of PHPT participants undergo parathyroidectomy?
  • The proportion of PHPT participants who complete surgical consultation?
  • Time to surgical consultation?
  • Time to surgery?

Detailed Description

Patients historically marginalized in Medicine are at increased risk of delayed care and undertreatment of PHPT, which can result in end-organ damage and reduced quality of life due to fatigue, brain fog, pain and other constitutional symptoms due to imbalances in calcium levels. It can be easily treated with a highly curative, cost-effective, and low risk surgery but less than 40% of patients who qualify for surgery undergo treatment. Patients from historically marginalized populations such as black/Hispanic/Asian race, underinsurance, and older age are disproportionately impacted by lower rates of surgery and longer delays to surgery. This pragmatic pilot trial aims to address surgical health equity in historically marginalized patients with PHPT by assessing the impact of navigation, specifically direct outreach and appointment scheduling, on conversion of surgical referral to consultation and conversion of surgical consultation to treatment in two dimensions, timeliness and clinical outcomes. Participants will be randomized to receive or not receive scheduling navigation at time of recruitment with a crossover design at 3 months for those who do not receive scheduling navigation at time of recruitment and have yet to complete surgical consultation.

Registry
clinicaltrials.gov
Start Date
February 1, 2026
End Date
December 30, 2026
Last Updated
3 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Rachel Kelz

Executive Vice Chair

University of Pennsylvania

Eligibility Criteria

Inclusion Criteria

  • Diagnosed with PHPT and not yet had parathyroidectomy who meet criteria for surgical treatment of PHPT (osteoporosis, fragility fracture, or evidence of vertebral compression fracture on spine imaging, renal involvement \[renal stone, silent nephrolithiasis on renal imaging, nephrocalcinosis, hypercalciuria (24-hour urine calcium level 400 mg/dL) with increased stone risk, or impaired renal function (glomerular filtration rate 60 mL/min)\], calcium 1 mg/dL above upper limit of normal, age less than 50)
  • Qualify as a member of a racial or ethnic minority group (Black, Hispanic, Asian and Pacific Islander, Native American), lower socioeconomic neighborhoods (by zipcode), socially vulnerable (social determinants of health indicating financial strain, social vulnerability index in the top quartile 75%+ by zip code), or with underinsurance (Medicaid, Medicare, dual eligible, uninsured)

Exclusion Criteria

  • Prior Parathyroidectomy
  • End-stage Renal Disease
  • Renal Transplant
  • Vitamin D Deficiency
  • Metastatic Disease
  • Familial Hypocalciuric Hypercalcemia
  • No Indication for Surgery
  • Unable/Unwilling to provide consent

Outcomes

Primary Outcomes

Parathyroidectomy Surgical Outcome

Time Frame: Within 12 months

The primary outcome will be the proportion of patients who undergo parathyroidectomy

Secondary Outcomes

  • Parathyroidectomy complications(Assessed at 6 and 12 months after recruitment or surgery in all groups)
  • Completion of Consultation(Through study completion, an average of 1 year after time of recruitment or surgery)
  • Time to Consultation(Through study completion, an average of 1 year after time of recruitment or surgery)
  • Time to Surgery(Through study completion, an average of 1 year after time of recruitment or surgery)
  • Complications related to hyperparathyroidism(Assessed at 6 and 12 months after recruitment or surgery in all groups)
  • Persistent hyperparathyroidism(Assessed at 6 and 12 months after recruitment or surgery in all groups)
  • Recurrent hyperparathyroidism(Assessed at 6 and 12 months after recruitment or surgery in all groups)
  • Surgical parathyroid re-exploration(Assessed at 6 and 12 months after recruitment or surgery in all groups)

Study Sites (2)

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