Fact CheckerSign in

NCT07388914Not yet recruiting

Aldosterone Variations in Patients With Primary Hyperparathyroidism After Surgery

Aldosterone Variations in Patients With Primary Hyperparathyroidism Before Surgery and in the Year Following Surgery for Parathyroid Disease.

Source: ClinicalTrials.gov · Last updated 5 Feb 2026

Brief summary (registry, in English)

Primary hyperparathyroidism is a disorder of calcium and phosphorus metabolism linked to dysfunction of one or more parathyroid glands. The latest recommendations from the American Association of Endocrine Surgeons (7) consider the presence of hypertension as an argument for proposing the removal of a parathyroid adenoma in the context of primary hyperparathyroidism. The renin-angiotensin-aldosterone system is involved in regulating blood pressure. The main objective of this study is to assess aldosterone level in patients with primary hyperparathyroidism before surgery and its variation in the year following surgery for parathyroid disease. Secondary objectives are to assess aldosterone variations after surgery at 3 months * Assess aldosterone variations after surgery at 6 months * Assess aldosterone variations after surgery at 12 months * Blood pressure changes before and after surgery (5 pre- and post-operative measurements) * Assess the number of antihypertensive treatments before and after surgery * Assess antihypertensive treatment according to the WHO-DDD classification before and after surgery Compare aldosterone levels in the 'primary hyperparathyroidism' group with a control group of patients from the general population (using the STANISLAS cohort). * Compare aldosterone levels in the HPT group with aldosterone levels in a group of patients after myocardial infarction (cardiovascular patient group )

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
400 (estimated)
First submitted
27 Jan 2026
Start date
1 Feb 2026
Primary completion date
Sept 2026
Lead sponsor
Central Hospital, Nancy, France
NCT number
NCT07388914

What you commit to

  • Study type: Observational
  • Planned participants: 400
  • From 1 Feb 2026 to the primary completion date, Sept 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Age

  • age\< 18 years patients with renal insufficiency (CKDEpi \<60ml/mn) pregant women

Other

  • \-

Who the study is looking for

  • patients with primary hyperparathyroidism candidate to surgery
  • age\>/=18 years

Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre Hospitalier Universitaire De Nancy
Coordinator of this site? Confirm its status
NancyFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.