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Hyperparathyroidism, Primary clinical trials

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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: NCT03027557 Completed - Clinical trials for Primary Hyperparathyroidism

Treatment of Primary Hyperparathyroidism With Denosumab and Cinacalcet.

DENOCINA
Start date: March 1, 2017
Phase: Phase 3
Study type: Interventional

The only known cure for primary hyperparathyroidism is surgical removal of one or more parathyroid glands. Some patients however, do not fulfill criteria for surgery or do not want to undergo a procedure due to fear of the associated risks. Therefore a medical alternative is warranted. This study aims to evaluate the effects of Denosumab alone, and in combination with Cinacalcet, as a medical treatment for patients suffering from primary hyperparathyroidism, with mild osteoporosis. To the best of our knowledge no previously reported randomized controlled trial has investigated the use of denosumab in primary hyperparathyroidism. 60 patients will be enrolled in three different treatment-groups: 20 receiving both Denosumab and Cinacalcet, 20 Denosumab and placebo and 20 placebo and placebo. Patients included do not meet the criteria for, or have no wish for a surgical procedure. By combining the two drugs, this study could possibly contribute to the discovery of a realistic medical alternative to surgery. It is expected that the therapy will be able to both control s-calcium and s-intact parathyroid hormone (iPTH), and simultaneously enhance bone-structure. The therapy thus has the potential of preventing fractures and possibly other long-term effects of primary hyperparathyroidism such as formation of kidney stones, and coronary calcification. Another objective of this project is to investigate whether the combined therapy can facilitate an actual reset of the Calcium-sensing receptor, and thereby de facto cure the disease.

NCT ID: NCT03011736 Completed - Clinical trials for Primary Hyperparathyroidism

Omission of Intact Parathyroid Hormone Testing During Surgery in Treating Patients With Primary Hyperparathyroidism

Start date: May 12, 2016
Phase: N/A
Study type: Interventional

This clinical trial studies the omission of intact parathyroid hormone testing during surgery in treating patients with primary hyperparathyroidism. Omission of intact parathyroid hormone testing during parathyroid gland removal may help patients with primary hyperparathyroidism to decrease their time under anesthesia, and decrease the overall time and cost of surgery.

NCT ID: NCT02989428 Completed - Clinical trials for Primary Hyperparathyroidism

Effect of Parathyroidectomy on Cardiovascular Health

Start date: February 3, 2017
Phase: N/A
Study type: Interventional

The aim of this study is to establish whether patients with mild primary hyperparathyroidism (PHPT) have an increased risk of cardiovascular diseases. The primary outcome is to determine whether arterial stiffness and blood pressure will decrease in patients with mild PHPT 3-month after parathyroidectomy (PTX).

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: NCT02711059 Withdrawn - Diabetes Clinical Trials

Insulin Resistance in Primary Hyperparathyroidism

IRIPH
Start date: October 2015
Phase: N/A
Study type: Interventional

The aims of this study is to analyse if insulin resistance in primary hyperparathyroidism (pHPT) is normalised after parathyroid adenomectomy and if glucose tolerance test may be useful as a diagnostic tool by predicting potential improvement of insulin sensitivity after biochemical cure of pHPT.

NCT ID: NCT02539498 Completed - Clinical trials for Primary Hyperparathyroidism

Bone Architectural Parameters in Postmenopausal Women Affected With Primary Hyperparathyroidism

MicrOs
Start date: April 2012
Phase: N/A
Study type: Interventional

Bone lesions are frequent in primary hyperparathyroidism (PHPT). Conventional measurement by Dual-Energy X-ray Absorptiometry does not provide enough information about the bone impact of excessive parathyroid hormone (PTH) secretion. High-Resolution peripheral Quantitative Computed Tomography (HR-pQCT) assesses separately cortical and trabecular bone sites as well as geometric characteristics of peripheral skeleton. In postmenopausal women, HR-pQCT has shown that decreased microarchitectural parameters are associated with reduced bone strength independently of BMD. The purpose of this study is to characterize the impact of PHPT in cortical and trabecular bone measured by HR-pQCT in postmenopausal women with PHPT followed for one year, in comparison with control postmenopausal women.

NCT ID: NCT02525796 Completed - Clinical trials for Primary Hyperparathyroidism

Evaluating Alternative Medical Therapies in Primary Hyperparathyroidism

Start date: January 2016
Phase: Phase 2/Phase 3
Study type: Interventional

This study will evaluate whether blocking the mineralocorticoid receptor, alone, or in combination with the calcimimetic cinacalcet, can lower parathyroid hormone and calcium levels in primary hyperparathyroidism.

NCT ID: NCT02417389 Completed - Osteoporosis Clinical Trials

Efficacy of Cinacalcet in the Control of Primary Hyperparathyroidism

CA-PHP
Start date: May 2008
Phase: Phase 4
Study type: Interventional

To assess the efficacy and safety of treatment with cinacalcet and with cinacalcet plus alendronate in controlling bone loss induced by primary hyperparathyroidism.