Evaluation of MRI and SPECT Fusion Software to Localize Parathyroid Adenomas
Stopped early
Conditions studied: Parathyroid Neoplasm, Parathyroid Diseases
In brief
The purpose of this study is to design a method to better localize parathyroid adenomas. This study will include approximately 6 patients who have not had surgery and another 25 patients who have already had surgery over the course of one year.
Key facts
- Study ID
- NCT00639405
- Run by
- State University of New York - Upstate Medical University
- People needed
- 12
- Starts
- 2005-09-01
- Expected to finish
- 2008-08-01
- Last updated by the study team
- 2011-04-27
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects who are 18 years and over
- subjects who have had a failed parathyroidectomy and now presents with persistent hyperparathyroidism or recurrent hyperparathyroidism
- 6 control patients with parathyroid adenomas who have not yet had surgery will be selected to test the efficacy of the software.
You may not qualify if…
- Potential female subjects who are pregnant
- Any potential subject who has an implanted metallic device, stent or staples
- any subject weighing 300lb
Where it is running
- SUNY Upstate Medical University — Syracuse, New York, United States
Full record on ClinicalTrials.gov
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