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Hyperparathyroidism clinical trials

View clinical trials related to Hyperparathyroidism.

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NCT ID: NCT03434067 Recruiting - Thyroidectomy Clinical Trials

The Application of Rapid PTH Test Paper in Operation of Hyperparathyroidism

Start date: January 1, 2018
Phase:
Study type: Observational [Patient Registry]

The half-life of the parathyroid hormone is about 4min, blood pth test is use in operation to confirm that parathyroid tumor is removed. but the blood pth test is time consuming and unpractical in most of hospital. this study will compare the application of rapid PTH test paper in operation of hyperparathyroidism.PTH test were measured in operation in different way. it will test at the time of preoperation, 15 minutes after surgery, 1 hour after surgery and 24 hours after surgery. thus evaluate the reliability and accuracy of PTH test paper in evaluating the Miami principles with the linear relation of blood PTH and the PTH test paper method.

NCT ID: NCT03203668 Recruiting - Hyperparathyroidism Clinical Trials

18F-fluorocholine PET/CT Imaging in Hyperparathyroidism

Start date: January 1, 2013
Phase: N/A
Study type: Interventional

To assess the efficiency of 18F-fluorocholine PET/CT in localization of hyperfunctioning parathyroid tissue in hyperparathyroidism, thereby enabling minimally invasive surgical approaches with fewer complications and comparable success rates

NCT ID: NCT03194087 Recruiting - Clinical trials for Secondary Hyperparathyroidism

the Study on Prognostic for Hemodialysis Patients

Start date: January 1, 2017
Phase: N/A
Study type: Observational

Results from KDOQI guidelines, parathyroid hormone (PTH) level within target range is 150-300pg/ml. Both lower PTH levels and higher PTH levels were associated with higher risk of all-cause mortality. However, in out of target range, it is still unknown which mortality higher. so, in this prospective, observational clinical trial study. the investigators will observe the mortality and cardiovascular incidence rate between SHPT(>800pg/ml) and low serum PTH levels(<60pg/ml). Both two groups of patients will receive a reasonable treatment according to the suggestions in K/DOQI guidelines.

NCT ID: NCT03082742 Recruiting - Clinical trials for Chronic Kidney Disease

The Effect of Diuretics on Mineral and Bone Disorder in Chronic Kidney Disease Patients

Start date: August 1, 2015
Phase: N/A
Study type: Interventional

Chronic kidney disease (CKD) patients often have associated systemic hypertension due to volume retention, as one of the mechanisms, therefore the use of diuretics is widespread in this population. One of the major complications of CKD is mineral and bone metabolism disorder (CKD-MBD), which include changes in the levels of calcium, phosphorus, vitamin D deficiency, increased circulating levels of fibroblast growth factor (FGF-23) and parathyroid hormone (PTH). These alterations are responsible for fractures, cardiovascular disease and mortality among patients with CKD. According to diuretic mechanism of action, sometimes increasing serum calcium (in the case of furosemide), sometimes decreasing it (in the case of thiazide), it is expected that the serum calcium may be altered, even within the range of normality, with consequent impact on the levels of PTH. Although most studies have shown that the use of thiazide diuretics decreases the risk of fractures, some showed the opposite. Similarly, although most studies have shown increased risk of fracture in association to loop diuretics use, some have failed in demonstrated this outcome. Only one study, a cohort study in a population of CKD, showed that furosemide was directly related to increased calciuria and PTH levels and the use of thiazide, in turn, showed completely opposite effect. However, certain issues are still not completely solved, for example, the interference of renal function itself on calciuria. It is possible that calciuria is not a so simple explanation that justifies the PTH levels changes, as no correlation was seen between calciuria and PTH levels. Better understanding of the exact relationship between the use of diuretics and the impact on CKD-MBD may be an alternative intervention, easily accessible and relatively inexpensive. The purpose of this study is to evaluate the impact of diuretic, specifically hydrochlorothiazide and furosemide, on bone architecture and mineral metabolism.

NCT ID: NCT03053999 Recruiting - Hyperparathyroidism Clinical Trials

Variables That Are Correlated to Developing Multiple Endocrine Neoplasia (MEN) and Pancreatic Neuroendocrine Tumors (PNET)

Start date: October 9, 2012
Phase:
Study type: Observational

The study aims to identify predictors of disease in patients with hyperparathyroidism (HPTH) who undergo surgery.

NCT ID: NCT03052075 Recruiting - Clinical trials for Primary Hyperparathyroidism

Percent Change in Baseline Bone Mineral Density (BMD) After Parathyroidectomy in Patients With Primary Hyperparathyroidism

Start date: September 3, 2014
Phase:
Study type: Observational

The primary objective of this study is to estimate the percent change in baseline bone mineral density (BMD) starting at one year after parathyroidectomy and all the following available dates in patients presenting with primary hyperparathyroidism. The secondary objective is to identify patient factors associated with change in BMD.

NCT ID: NCT03039439 Recruiting - Clinical trials for Primary Hyperparathyroidism

Molecular and Immunohistochemical Profiling of Tumors in Patients With Parathyroid Tumors

Start date: November 24, 2015
Phase:
Study type: Observational

This trial studies molecular and immunohistochemical profiling of tumors in patients with parathyroid tumors. Studying molecular and immunohistochemical profiling of tumors may help doctors avoid inconsistencies in diagnosis, unnecessary or incomplete surgery, surgical morbidity, psychological stress, and inadequate follow up.

NCT ID: NCT02986607 Recruiting - Hyperparathyroidism Clinical Trials

Corticosteroid Rhythms in Hypoparathyroid Patients

Start date: March 2016
Phase: Early Phase 1
Study type: Interventional

The investigators hypothesise that parathyroid hormon (PTH) depletion interferes with normal activity of the hypothalamus-pituitary-adrenal (HPA)-axis and the renin-angiotensin-aldosterone-system (RAAS), which in turn may impact morbidity and quality of life. The main objective of the current study is to test if PTH deficiency influences the secretion of corticosteroids and whether any abnormalities in the HPA-axis and the RAAS-system can be reversed by PTH infusion.

NCT ID: NCT02854345 Recruiting - Clinical trials for Primary Hyperparathyroidism

Preliminary Study Concerning the Validity of Parathyroid Exploration on a CZT Camera

PARAT-CZT
Start date: September 2014
Phase: N/A
Study type: Interventional

The goal of this study is to assess the performance of parathyroid imaging on a cardiac-dedicated CZT camera, compared to planar pinhole imaging, in patients referred for primary hyperparathyroidism.

NCT ID: NCT02332135 Recruiting - Clinical trials for Secondary Hyperparathyroidism

The Efficacy and Safety of Microwave Ablation for Mild-to-moderate Secondary Hyperparathyroidism Patients Undergoing Hemodialysis

Start date: January 2015
Phase: N/A
Study type: Interventional

Microwave ablation, as a new method to therapy secondary hyperparathyroidism(SHPT), now is developing rapidly. However, it is still unknown whether it is effective to accept microwave ablation for hemodialysis patients with mild-to-moderate SHPT. In this prospective, randomised control and paried clinical trial study, the investigators will observe the efficiency and safety of microwave ablation in hemodialysis patients with mild-to-moderate secondary hyperparathyroidism. The patients in age-matched control group will accept active Vitamin D therapy.