Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05793853

Hypoparathyroidism Natural History Study

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

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Columbia University Medical Center - Harkness Pavillion

New York, 10032, United States

Location status: Recruiting

Location contact

Mishaela Rubin, MD

PRINCIPAL_INVESTIGATOR

Noelle Texeira

CONTACT

[email protected]

212-305-2801

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • An understanding, ability and willingness to fully comply with study procedures and restrictions.
  • Ability to voluntarily provide written, signed and dated informed consent as applicable to participate in the study.
  • Male or female ≥18 years of age with HPT. All HPT sub-types are eligible, including surgical (HPT-S) and nonsurgical (HPT-NS) HPT: autoimmune, genetic (including but not limited to: DiGeorge syndrome, autoimmune polyendocrine syndrome type 1, hypoparathyroidism sensorineural deafness and renal disease syndrome, Kearns-Sayre syndrome, mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes [MELAS] syndrome, mitochondrial trifunctional protein [MTP] deficiency syndrome, Kenny-Caffey syndrome, Sanjad-Sakati syndrome, autosomal dominant hypocalcemia), infiltrative (granulomatous), mineral deposition (copper, iron), metastatic, radiation and idiopathic HPT.
  • Diagnosis of HPT established based on historic hypocalcemia in the setting of inappropriately low serum PTH levels on two occasions.
  • All treatment regimens are permitted, including but not limited to conventional management with calcium (e.g. calcium citrate, calcium carbonate, etc), active vitamin D (calcitriol, alfacalcidol), parent vitamin D, magnesium, phosphate binders and thiazides. Use of PTH-like drugs are permitted.

Exclusion criteria

  • Functional HPT
  • Transient HPT
  • Pseudohypoparathyroidism
  • Pregnancy

Treatment and study plan

Primary outcomes

  1. Kidney function

    Time frame: baseline, 6, 12, 18, 24, 30, 36 Months

    blood test for changes in eGFR (in mL/min/1.73m^2)

Secondary outcomes

  1. Kidney calcification

    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.

  2. Brain calcification

    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.

  3. Vascular calcification

    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

  4. Bone mineral density

    Time frame: Baseline and 36 Months

    Changes in dual energy X-ray absorptiometry will be assessed in an optional imaging sub-group

  5. Bone microarchitecture and bone strength

    Time frame: Baseline and 36 Months

    Changes in high resolution peripheral quantitative computed tomography will be assessed

  6. Cardiac function

    Time frame: Baseline and 36 Months

    Changes in EKG will be assessed

  7. Transcriptomic signaling for calcification

    Time frame: Baseline and 36 Months

    Changes in microRNA will be assessed

  8. Biomarkers blood

    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.

  9. Biomarkers urine

    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

  10. Dietary Intake

    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

  11. Cognitive Function

    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

  12. Neurologic Tests of Motor Function

    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

  13. Quality of Life Through Self-Reported Questionnaires

    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

  14. Calcioprotein Maturation Time

    Time frame: Baseline and 36 months

    Will be obtained through blood collection and measured in minutes and changes will be tracked through visits

  15. Sclerostin

    Time frame: Baseline and 36 months

    Will be obtained through blood collection and measured in pmol/L and changes will be tracked through visits

  16. FGF23

    Time frame: Baseline and 36 months

    Will be obtained through blood collection and measured in pg/mL and changes will be tracked through visits

Study contacts

Contact information is provided by the study sponsor or research team.

Aastha Mehta

CONTACT

[email protected]

212-342-0132

Noelle Texeira

CONTACT

[email protected]

212-305-2801

Sponsors and collaborators

Lead sponsor

Columbia University

Other

Registry information

Official study title

Advancing Product Development for Hypoparathyroidism: A Prospective Natural History Study of the Clinical Outcomes and Regulation of Disordered Mineral Metabolism

Acronym: SHINE

Important dates

Study start
2022
Primary completion
2026
Study completion
2026
First posted
Mar 31, 2023
Registry last updated
Dec 16, 2025

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.

Published trials that share one or more normalized conditions with this study.