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CompletedNCT01409798Updated Sep 26, 2024

The Midwest Head and Neck Cancer Consortium Multi-Institutional Parathyroid Registry

An observational study in Primary Hyperparathyroidism, sponsored by University of Nebraska. Completed at 6 sites in United States. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2024-09-26.

Sponsored by University of Nebraska · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
175
Ages
19 Years and older
Sex
All
01

Study summary

The purpose of this registry is to create a database that collects clinical data to improve knowledge about primary hyperparathyroidism.

Read the detailed description

This will be a multi-institutional prospective study in which patients that have undergone parathyroidectomy with intra-operative PTH assessment. The success of minimally invasive parathyroidectomy without and with intra-operative PTH will be assessed for each patient. Success for exploration without intra-operative PTH will be defined as directed exploration with detection of an abnormal parathyroid in the location suggested by imaging. Success with intra-operative PTH will be defined as per standard protocols (50% or > decrease in intra-operative PTH following excision).

02

Conditions studied

  • Primary Hyperparathyroidism

Keywords

  • Hyperparathyroidism
  • Hypercalcemia
03

In context

Hyperparathyroidism, Primary

105 studies on the registry are indexed under Hyperparathyroidism, Primary; 23 are open to participants now.

This study's enrollment of 175 is above the median of 145 across 42 observational studies indexed under Hyperparathyroidism, Primary.

Browse Hyperparathyroidism, Primary studies →

Lead sponsor

University of Nebraska is the lead sponsor of 495 studies on the registry; 68 are open to participants now.

Of its 83 completed or terminated interventional studies of FDA-regulated products, 52 (63%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Otolaryngology, Head and Neck Surgery clinic patients

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult individuals (male and female) who have a personal diagnosis/history of primary hyperparathyroidism.
  • Age 19 or greater.
  • Patients who are seen and treated surgically at UNMC's Department of Otolaryngology- Head Neck Surgery .
  • Able to provide informed consent.

Exclusion criteria

Exclusion Criteria:

-No history of primary hyperparathyroidism

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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
175 participants (actual)
06

Study locations

6 sites
  • University of Iowa
    Iowa City, Iowa 52242, United States
  • Kansas University Medical Center
    Lawrence, Kansas 66160, United States
  • University of Minnesota
    Minneapolis, Minnesota 55414, United States
  • University Of Missiouri
    Columbia, Missouri 65212, United States
  • University of Nebraska Medical Center
    Omaha, Nebraska 681225, United States
  • Sanford School of Medicine
    Sioux Falls, South Dakota 57105, United States
07

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jun 2010 to primary completion in Dec 2014, 53 months.

Of 18 observational studies under Hyperparathyroidism, Primary, half reached primary completion within 41 months of starting (the median), counting those still running; a quarter within 24 and three quarters within 69. This study's 53 months is above that.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 2, 2011
First posted
Aug 4, 2011
StartActual
Jun 9, 2010
Primary completionActual
Dec 1, 2014
CompletionActual
Apr 27, 2015
Last update
Sep 26, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 26, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01409798
Responsible party
Sponsor
First posted
Aug 4, 2011
Start date
Jun 9, 2010
Primary completion
Dec 1, 2014
Completion
Apr 27, 2015
Last update
Sep 26, 2024

Study contacts

Russell B Smith, MD
principal investigator · University of Nebraska

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2024. You cannot join it, but the record below documents what was studied.

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Discussion

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