Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06562881

Patient Navigation to Improve Surgical Access in Primary Hyperparathyroidism

Led by University of Pennsylvania · Updated on 2026-03-19

76

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

Sponsors

U

University of Pennsylvania

Lead Sponsor

A

American College of Surgeons

Collaborating Sponsor

AI-Summary

What this Trial Is About

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?

CONDITIONS

Official Title

Patient Navigation to Improve Surgical Access in Primary Hyperparathyroidism

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with primary hyperparathyroidism (PHPT) and not yet had parathyroidectomy who meet criteria for surgical treatment (osteoporosis, fragility fracture, vertebral compression fracture, renal involvement, calcium 1 mg/dL above upper limit, or age less than 50)
  • Qualify as a member of a racial or ethnic minority group (Black, Hispanic, Asian and Pacific Islander, Native American)
  • Live in lower socioeconomic neighborhoods (by zipcode) or have social vulnerability (top quartile 75%+ by social determinants or zip code)
  • Have underinsurance (Medicaid, Medicare, dual eligible, uninsured)
Not Eligible

You will not qualify if you...

  • Prior parathyroidectomy
  • End-stage renal disease
  • Renal transplant
  • Vitamin D deficiency
  • Metastatic disease
  • Familial hypocalciuric hypercalcemia
  • No indication for surgery
  • Unable or unwilling to provide consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hospital of the University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

J

Jasmine Hwang, MD

CONTACT

R

Rachel Kelz, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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