Creating a national database for patients with parathyroid cancer and atypical adenoma in Italy

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to establish and manage a multicenter national database for patients diagnosed with parathyroid carcinoma or atypical parathyroid adenoma across Italy. The study will involve 33 specialized clinical centers and will collect both retrospective and prospective data over a 10-year period. Information gathered will include clinical, genetic, diagnostic, and therapeutic data to enhance understanding and management of these rare conditions. The goal is to refine clinical guidelines and improve patient outcomes through comprehensive data analysis.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Cohort 1: parathyroid carcinoma
* Cohort 2: atypical parathyroid adenoma

Exclusion Criteria:

None

Where it's running

• UO Endocrinologia e Malattie del Ricambio, Azienda Ospedaliero Universitaria di Ferrara, Sezione di Endocrinologia, Geriatria e Medicina Interna, Dipartimento di Scienze Mediche, Università degli Studi di Ferrara
  Ferrara, Italy Recruiting
• SOD Malattie del Metabolismo Minerale ed Osseo, Azienda Ospedaliero-Universitaria Careggi
  Florence, Italy Recruiting
• Dipartimento di Medicina Clinica e Chirurgia; Unità di Endocrinologia, Diabetologia e Andrologia; Università degli Studi di Napoli Federico II
  Naples, Italy Recruiting
• Donatello Bone Clinic, Casa di Cura Villa Donatello
  Sesto Fiorentino, Italy Recruiting
• U.O.C. Endocrinologia, Azienda Ospedaliero Universitaria Policlinico Consorziale, Università degli Studi di Bari "Aldo Moro"
  Bari, Italy Not yet recruiting
• UOC Endocrinologia e Prevenzione e Cura del Diabete, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Dipartimento di Scienze Mediche e Chirurgiche (DIMEC), Alma Mater Studiorum Università di Bologna
  Bologna, Italy Not yet recruiting

Study contacts

• Study coordinator: Maria Luisa Brandi, MD, PhD
• Email: marialuisa@marialuisabrandi.it
• Phone: 0039-055-2336663

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.