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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06419270
Other study ID # VK-1-10-72-169-23
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 2024
Est. completion date December 2028

Study information

Verified date April 2024
Source University of Aarhus
Contact Sarah Thornhoj
Phone 40491821
Email sarthorn@rm.dk
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this observational study is to learn about long term effects to post surgical hypoparathyroidism. The main questions are: 1. Patients with hypoparathyroidism do not have an increased arterial stiffness compared to healthy controls. 2. Patients with hypoparathyroidism do not have an increased coronary artery plaque burden assessed by cardiac CT compared to healthy controls. 3. Patients with hypoparathyroidism do not have an increased prevalence of vertebral fractures compared to healthy controls. Results will be compared with gender and age matched controls from the general population. Participants will have a CT scan, DXA scan, tonometry, blood samples and questionaries performed and collect a 24-hour urine sample.


Description:

Hypoparathyroidism is a rare endocrine disorder characterized by hypocalcemia with low or undetectable levels of parathyroid hormone. The most common cause of hypoparathyroidism is following neck surgery, whereas approximately 25% of hypoparathyroidism patients are suffering from non-surgical hypoparathyroidism due to e.g., genetic or autoimmune causes. According to updated international guidelines, the condition is considered chronic if treatment with calcium and activated vitamin D is still needed a year after surgery. A large retrospective cohort study of patients with chronic hypoparathyroidism shows that patients with chronic hypoparathyroidism have a significantly higher risk of cardiovascular disease, compared to patients without hypoparathyroidism. Additionally, it is well known that patients with hypoparathyroidism are at increased risk of renal and extra-skeleton calcifications, although cardiovascular calcifications are only sparsely investigated. Furthermore, both higher arterial stiffness assessed by pulse wave velocity and an increased heart rate have previously been shown in patients with non-surgical hypoparathyroidism. It is largely unknown whether this also applies to patients with post-surgical hypoparathyroidism. The overall aim of the project is to investigate cardiovascular, renal, and skeletal indices in patients diagnosed with Post Surgical hypoparathyroidism and test the following (null-)hypotheses: 1. H0: Patients with post-surgical hypoparathyroidism do not have an increased arterial stiffness compared to healthy controls. 2. H0: Patients with post-surgical hypoparathyroidism do not have an increased coronary artery plaque burden assessed by cardiac CT compared to healthy controls. 3. H0: Patients with post-surgical hypoparathyroidism do not have an increased prevalence of vertebral fractures compared to healthy controls. Patients and controls who accept participation will undergo a detailed examination in terms of: Medical history, physical examination, questionnaires, blood and 24-hour urine samples, DXA scan, HRpQCT, tonometry, 12-lead electrocardiogram, 24-hour blood pressure and a CT scan Data are analyzed according to their distribution using parametric or non-parametric statistics. To address the hypotheses, statistical power calculations have been performed. 50 patients with post-surgical hypoparathyroidism will be matched on sex and age (± 2 years) with 50 randomly selected otherwise healthy controls from the general population.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date December 2028
Est. primary completion date May 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: Patients only: - Chronic post surgical hypoparathyroidism diagnosed > 5 years ago. (In case recruitment is too challenging, we will accept duration of disease of minimum one year. Including patients with longest duration of disease first.) - Require treatment with active vitamin D = 1 µg/day Controls only: - No history of neck surgery - No history of parathyroid disease All participants: - Age = 18 years - 25(OH)D vitamin = 50 nmol/L - Serum magnesium = 0,50 mmol/L - Able to read and understand Danish - Willing and able to sign the informed consent form Exclusion Criteria: - Estimated glomerular filtration rate (eGFR) < 30 ml/min/1.73 m3 - Active cancer or former (except thyroid and basal cell skin) cancer treatment < 5 year ago - Pregnancy, or breastfeeding < 1 year ago - Untreated thyroid or liver diseases during the last year - Treatment with lithium within the last 4 weeks - Known allergy or sensitivity to iodine - Any reason that in the opinion of the investigator, that would prevent the patient from completing the study.

Study Design


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of Aarhus Gødstrup Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Arterial stiffness aortic pulse wave velocity in m/s 24 months
Primary Vertebral fractures VFA assessing fractures in numbers 24 months
Primary coronary artery plaque burden Heart CT scan assessing coronary artery calcium score 24 months
Secondary Renal indices Description of calcifications 24 months
Secondary bone indices Description of bone status 24 months
Secondary Cardiovascular indices Description of calcifications 24 months
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