Registry for patients with parathyroid disease
Establishment of a Registry of Patients With Parathyroid Disease
This study is creating a detailed registry for people with parathyroid disorders to collect important health information over 30 years to help with future research.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna Academic / other |
| Locations | 1 site (Bologna, Bologna) |
| Trial ID | NCT06797934 on ClinicalTrials.gov |
What this trial studies
This study aims to establish a comprehensive registry for patients diagnosed with parathyroid disorders, specifically hyperparathyroidism and hypoparathyroidism, at the O.U. Endocrinology. Patients will be enrolled consecutively after at least two endocrinology visits, and the registry will collect longitudinal data over a 30-year period. The data will include biochemical, clinical, radiological, and histological information to facilitate future research and evaluations.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older diagnosed with hyperparathyroidism or hypoparathyroidism.
Not a fit: Patients without a diagnosis of parathyroid disease or those who do not meet the inclusion criteria will not benefit from this study.
Why it matters
Potential benefit: If successful, this registry could enhance understanding and management of parathyroid diseases, leading to improved patient outcomes.
How similar studies have performed: While similar registries have been established for various conditions, this specific approach for parathyroid disease is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age ≥18 years * Diagnosis of hyperparathyroidism or hypoparathyroidism based on biochemical parameters (calcemia, parathormone, phosphormia, creatinine, albumin, vitamin D25OH) * Obtaining informed consent Exclusion Criteria: * none
Where this trial is running
Bologna, Bologna
- IRCCS Azienda Ospedaliero-Universitaria di Bologna — Bologna, Bologna, Italy (Recruiting)
Study contacts
- Principal investigator: Uberto Pagotto, MD — IRCCS Azienda Ospedaliero-Universitaria di Bologna
- Study coordinator: Uberto Pagotto, MD
- Email: uberto.pagotto@unibo.it
- Phone: +390512144190
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.