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Hyperparathyroidism, Primary clinical trials

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NCT ID: NCT04299425 Completed - Clinical trials for Primary Hyperparathyroidism

Evaluating Impact of NIRAF Detection for Identifying Parathyroid Glands During Parathyroidectomy

NIRAF
Start date: March 13, 2020
Phase: N/A
Study type: Interventional

This study describes a single center, randomized, single-blinded clinical trial to assess the clinical benefits of the use of near infrared autofluorescence (NIRAF) detection with an FDA-cleared device 'Parathyroid Eye (PTeye)' for identifying parathyroid glands (PGs) during parathyroidectomy (PTx) procedures. It compares risk-benefits and outcomes in PTx patients where NIRAF detection with PTeye for parathyroid identification is either used or not used.

NCT ID: NCT04126954 Not yet recruiting - Clinical trials for Hyperparathyroidism, Secondary

Study on the Use of Cinacalcet in Phosphocalcic Context.

CALCI-CINA
Start date: January 2020
Phase:
Study type: Observational

Currently, the indications used for MA (Marketing Authorization) Cinacalcet in France are hyperparathyroidism (hyperPTH) in adults, whether primary (for patients in whom parathyroidectomy is theoretically indicated but in whom it is contraindicated or not is not clinically appropriate) or secondary to a chronic kidney disease, and parathyroid carcinomas. In pediatric patients, data on its use are restricted due to its recent marketing authorization (2017) and limited to dialysis patients suffering from secondary hyperPTH. Nevertheless, some patients with phosphocalcic pathologies without renal insufficiency must be treated off-label by cinacalcet in the presence of severe hyperPTH, without any other chronic treatment available to date. The objective of this study is therefore to evaluate the use in France of cinacalcet in phosphocalcic pathologies without renal insufficiency, in order to obtain efficacy and safety data in order to improve our knowledge on the management of these orphan diseases.

NCT ID: NCT04085419 Enrolling by invitation - Osteoporosis Clinical Trials

Osteoporosis in Primary Hyperparathyroidism

Start date: May 8, 2019
Phase: Phase 4
Study type: Interventional

Investigators will prospectively include 40 postmenopausal women with secondary osteoporosis due to primary hyperparathyroidism who have refused surgery. Participants will be randomized in two groups and treated either with zoledronic acid 5 mg iv once a year or with denosumab 60 mg sc every 6 months. Investigators will compare the effect of both drugs on bone turnover markers and basic laboratory parameters after 3, 12 and 24 months of treatment, and on the bone mineral density after 12 and 24 months of treatment. All participants will take cholecalciferol 800 - 1000 IU daily.

NCT ID: NCT04040946 Completed - Hyperparathyroidism Clinical Trials

Trial Comparing 2 Diagnostic Strategies for Preoperative Localization of Parathyroid Adenoma in Primary Hyperparathyroidism:TEMP / CT With Tc99m-sestaMIBI or PET / CT With F18-choline in First Intention

APACH2
Start date: September 19, 2019
Phase: Phase 3
Study type: Interventional

The investigators hypothesize that positron emission tomography with fluorocholline (F18-choline PET) will reduce the proportion of unnecessary invasive surgery decisions and that the higher cost of positron emission tomography versus MIBI scintigraphy (Tc99m-sestaMIBI ) will be offset by lower cost in terms of type. surgery performed wisely and complications.

NCT ID: NCT04013100 Terminated - Clinical trials for Primary Hyperparathyroidism

Cohort Trial on Perioperative Localization Techniques of Parathyroid Adenomas

ParaCatI
Start date: January 1, 2014
Phase:
Study type: Observational [Patient Registry]

A prospective database of consecutive patients with hyperparathyroidism subject to surgery is created. Preoperative workup and operative findings are recorded in this registry to allow comprehensive analysis.

NCT ID: NCT03968510 Completed - Hyperparathyroidism Clinical Trials

Swalqol in Primary Hyperparathyroidism

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

Swallow related quality of life before and after parathyroidectomy will be evaluated in patients with primary hyperparathyridism.

NCT ID: NCT03935984 Recruiting - Clinical trials for Primary Hyperparathyroidism

Calcitonin Pre-treatment to Improve SPECT-CT Sensitivity

Start date: May 29, 2019
Phase: Phase 4
Study type: Interventional

Patients with biochemically confirmed primary hyperparathyroidism and non-localizing SPECT-CT exam within the past year will be included. Subjects will be treated with calcitonin to lower calcium levels immediately prior to reimaging. The goal of this study is to determine whether lowering calcium will improve uptake/retention of sestamibi and improve sensitivity of SPECT-CT to localize parathyroid adenoma.

NCT ID: NCT03931109 Active, not recruiting - Clinical trials for Osteoporosis, Postmenopausal

Circulating miRNA in Primary Hyperparathyroidism

Start date: September 7, 2018
Phase:
Study type: Observational [Patient Registry]

The goal of this study is to: 1. Analyze the expression levels of circulating (serum) miRNAs in primary hyperparathyroidism patients with and without osteoporosis, and patients with osteoporosis undergoing thyroidectomy, and to correlate with clinical markers of bone remodeling including biochemical and radiologic studies. 2. To evaluate serum miRNA levels after treatment with parathyroidectomy.

NCT ID: NCT03831620 Completed - Clinical trials for Primary Hyperparathyroidism

The Crosstalk Between Calcium-sensing Receptor Signaling and Endocannabinoid System in Primary Hyperparathyroidism

Targeting CaSR
Start date: February 1, 2019
Phase:
Study type: Observational [Patient Registry]

Despite the strong association of hyperparathyroidism with arachidonic acid related lipid signals, little research has been performed over the years. A better understanding of the link between arachidonic acid remodeling, prostaglandin and endocannabinoid production with primary hyperparathyroidism in primary tissue/cells might open up new avenues for biomarker and thus to a potential therapeutic target. Arachidonic acid remodeling might also have an impact on depression and elevated cytokines in patients with primary hyperparathyroidism. The investigators therefore will assess the correlation between postoperative improvement of PHQ-9 and cytokine levels with arachidonic acid remodeling.

NCT ID: NCT03776058 Completed - Clinical trials for Primary Hyperparathyroidism

Safety, Tolerability, and Clinical Effects of Twice-daily Doses of Cinacalcet (AMG 073) in Adults With Primary Hyperparathyroidism (HPT)

Start date: June 15, 2000
Phase: Phase 2
Study type: Interventional

The primary objectives were to assess the safety and tolerability of twice daily (BID) doses of 65 mg cinacalcet administered orally to adults with primary HPT.