Columbia University Medical Center - Harkness Pavillion
New York, 10032, United States
Location status: Recruiting
NCT Number: NCT05793853
This is a prospective three-year natural history study of adults with hypoparathyroidism. The goal is to monitor patients with hypoparathyroidism to define end-organ damage in the context of the disease.
The study objectives are to:
1. Build a prospective cohort of patients to study HPT-associated end-organ damage. 2. Determine end-organ physiologic consequences of HPT. 3. Elucidate determinants of HPT-associated end-organ damage.
Funding Source - FDA OOPD
Interested in participating?
Request Info18 year–100 year
All sexes
Observational
New York, 10032, United States
Location status: Recruiting
The goal of this study is to prospectively collect data on the natural history of hypoparathyroidism (HPT). This will enable longitudinal data collection of complications in this disease, specifically defining the epidemiology of end-organ complications of HPT that are related to high calcification propensity. It will also determine relationships between calcification burden and end-organ disease severity and progression risk and assess the utility of traditional and novel biomarkers of mineral and bone metabolism on disease diagnosis and monitoring. These data will inform future investigations on the development, study, and implementation of HPT end-organ disease modifying strategies and impact clinical practice in hypoparathyroidism.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: baseline, 6, 12, 18, 24, 30, 36 Months
blood test for changes in eGFR (in mL/min/1.73m^2)
Time frame: Baseline and 36 Months
Changes in kidney calcification and stones will be assessed by abdominal CT in an optional imaging sub group. Results will be assessed and reported by a clinician.
Time frame: Baseline and 36 Months
Changes in brain calcification will be assessed by head CT in an optional imaging sub-group. Results will be assessed and reported by a clinician.
Time frame: Baseline and 36 Months
Changes in vascular calcification will be assessed by leg arterial calcifications on high resolution quantitative computed tomography in all, and aortic calcifications on abdominal CT and vertebral fracture assessment by DXA in optional imaging sub-group
Time frame: Baseline and 36 Months
Changes in dual energy X-ray absorptiometry will be assessed in an optional imaging sub-group
Time frame: Baseline and 36 Months
Changes in high resolution peripheral quantitative computed tomography will be assessed
Time frame: Baseline and 36 Months
Changes in EKG will be assessed
Time frame: Baseline and 36 Months
Changes in microRNA will be assessed
Time frame: baseline, 6, 12, 18, 24, 30, 36 Months
Changes in complete metabolic panel to see changes with eGFR (including albumin-corrected serum calcium), PTH, phosphorus, magnesium, 25(OH)D, 25(OH)D2, TSH, FT4.
Time frame: baseline, 6, 12, 18, 24, 30, 36 Months
24 hour urine will be collected for changes in calcium, creatinine, total volume and protein
Time frame: baseline, 12, 24 and 36 Months
Food frequency questionnaires will be administered to measure changes in calcium, phosphorus, vitamin D, and sodium intake
Time frame: baseline, 12, 24 and 36 Months
Changes in cognitive function will be assessed by NIH Toolbox®; Letter Fluency by the Controlled Oral Word Association Test with the letters FAS; Sematic Fluency by Animal Fluency; List Learning and Memory by the Hopkins Verbal Learning Test; subjective cognitive function by FACT-Cog
Time frame: baseline, 12, 24 and 36 Months
Repeated Chair Stand (RCS) test will be administered to see how many times a patient can sit in and stand from a chair in 30 seconds and "Timed Up and Go" Test will measure how many seconds it takes for a patient to walk to assess changes in motor function
Time frame: baseline, 12, 24 and 36 Months
Quality of life will be assessed by SF-36, FACIT-IF (self-reported fatigue), PGI-S and PGI-I (patient global impression of severity and impact), Hospital Anxiety and Depression Scale (HADS) and the HPT Symptom Diary and changes will be tracked through visits
Time frame: Baseline and 36 months
Will be obtained through blood collection and measured in minutes and changes will be tracked through visits
Time frame: Baseline and 36 months
Will be obtained through blood collection and measured in pmol/L and changes will be tracked through visits
Time frame: Baseline and 36 months
Will be obtained through blood collection and measured in pg/mL and changes will be tracked through visits
Contact information is provided by the study sponsor or research team.
Aastha Mehta
CONTACT
Noelle Texeira
CONTACT
Columbia University
Other
Advancing Product Development for Hypoparathyroidism: A Prospective Natural History Study of the Clinical Outcomes and Regulation of Disordered Mineral Metabolism
Acronym: SHINE
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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