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Procedure

Parathyroid surgery for Primary Hyperparathyroidism (MIRP Trial)

N/A
Waitlist Available
Led By Michael J Flynn, M.D.
Research Sponsored by University of Louisville
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
* All patients with biochemical evidence of primary hyperparathyroidis
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group

Summary

The main purpose of this research study is to evaluate the effectiveness of a minimally invasive surgical approach to removing parathyroid gland(s). The researchers are also interested in analyzing abnormal parathyroid tissue for changes in genes and proteins that may contribute to overactive parathyroid gland(s).

Eligible Conditions
  • Primary Hyperparathyroidism

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Parathyroid surgeryExperimental Treatment1 Intervention
Database of patients who have undergone minimally invasive radioguided parathyroidectomy
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Minimally invasive radioguided parathyroidectomy
1998
N/A
~860

Find a Location

Who is running the clinical trial?

University of LouisvilleLead Sponsor
345 Previous Clinical Trials
76,559 Total Patients Enrolled
Norton HealthcareOTHER
15 Previous Clinical Trials
1,857 Total Patients Enrolled
Jewish Hospital and St. Mary's HealthcareOTHER
4 Previous Clinical Trials
93 Total Patients Enrolled
~32 spots leftby Nov 2025
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