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Heart FailureCVD-PHPTNCT07870369

Cardiovascular Risk in Patients With Primary Hyperparathyroidism

An observational study of Heart Failure and Atrial Fibrillation (AF), run by Medical University of Sofia at 1 site in Bulgaria.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

Patients with primary hyperparathyroidism versus healthy controls assessed for their cardiovascular risk and overt CVD Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
How many people
77 participants
Where
1 siteBulgaria
Study dates
1 Jan 2023to 31 Dec 2025
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: 54 patients with PHPT and 23 controls

Who may be able to join

  • confirmed primary hyperparathyroidism

Who cannot join

  • secondary hyperparathyroidism

Trial locations and contacts

1 site in 1 country.

Bulgaria1 site
  • KPVB

    Sofia, 1680

Other trials in Bulgaria

About this study

Patients with primary hyperparathyroidism versus healthy controls assessed for their cardiovascular risk and overt CVD

Read the detailed description

A cross-sectional, non-interventional single-center study includding 54 patients with primary hyperparathyroidism and 23 healthy controls. The participants have been examined clinically and with certain instrumental investigations: laboratorys, ECG, Holter ECG echocardiography. We have evaluated comparatively the cardiovascular risk and the over cardiac events in both groups and sought for determinants of cardiaovascular complications in primary hyperparathyoridism.

Keywords
primary hyperparathyoidism, cardiovascular, risk, arrhythmias, hypertension, heart failure
Medical subject headings
Heart Failure, Atrial Fibrillation, Arrhythmias, Cardiac, Coronary Artery Disease, Hypertension

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07870369
Study groupRoleWhat they receive
Primary hyperparathyroidismPatients with primary hyoerparathyroidism
Control groupPatients withthout primary pyperparathyroidism mateched for age and sex

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Cardiovascular events

    Any cardiac events

    Measured: 24 months

  2. Cardiovascular complications

    Any cardiovascular disease

    Measured: january 1st 2023 - december 31st 2025

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Oct 2026
  2. Study start1 Jan 2023
  3. Primary completion31 Dec 2025
  4. Study completion31 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
77 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07870369
Sponsor's protocol ID
PHPT-CVD-2023
Acronym
CVD-PHPT
Status last verified
Oct 2026
First submitted
6 Oct 2026
Last updated
13 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

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