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Clinical Trial Summary

The primary objective of this study is to estimate the percent change in baseline bone mineral density (BMD) starting at one year after parathyroidectomy and all the following available dates in patients presenting with primary hyperparathyroidism. The secondary objective is to identify patient factors associated with change in BMD.


Clinical Trial Description

The research plan is for a retrospective review to be performed of a prospectively maintained parathyroid database within the Department of Surgical Oncology at the University of Texas MD Anderson Cancer Center. The patient cohort for this study consists of all patients with primary hyperparathyroidism who underwent parathyroidectomy and also had pre- and post-operative DEXA studies performed. The database will be reviewed to obtain patient and disease characteristics, laboratory values, DEXA imaging results, and surgical outcomes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03052075
Study type Observational
Source M.D. Anderson Cancer Center
Contact Nancy D. Perrier, MD
Phone 713-792-6940
Email NPerrier@mdanderson.org
Status Recruiting
Phase
Start date September 3, 2014
Completion date September 30, 2020

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