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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03027349
Other study ID # Primary hyperparathyroidism
Secondary ID
Status Completed
Phase N/A
First received January 18, 2017
Last updated February 14, 2017
Start date January 2011
Est. completion date February 2017

Study information

Verified date February 2017
Source Azienda USL Modena
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Background:

Primary hyperparathyroidism (PHPT) is often overlooked and underdiagnosed. At present the diagnosis of PHPT remains challenging and is based on serum calcium (Ca) and PTH.

As serum Ca and phosphorous (P) are inversely related in PHPT, the Ca/P ratio might be considered a good candidate tool in the diagnosis of PHPT.

AIM: The aim of this study is to investigate the diagnostic value of the Ca/P ratio in the diagnosis of PHPT.

Study design: Retrospective, observational, cross-sectional, case-control clinical trial will be carried out.

Biochemical measurements will include PTH, Vitamin D, serum Ca, P, albumin, and creatinine.


Recruitment information / eligibility

Status Completed
Enrollment 180
Est. completion date February 2017
Est. primary completion date February 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- elevated parathormone serum levels

- normal or elevated calcium serum levels

Exclusion Criteria:

- age younger than 18 years

- renal and liver failure and insufficiency

- active metabolic bone disease (such as Paget's disease of the bone, osteomalacia, rickets, etc)

- any type of cancer

- malnutrition, severe obesity (BMI > 40 kg/m2) and malabsorption

- transplantation

- sarcoidosis

- endocrinological disorders such as hypercortisolism, diabetes insipidus, hyperthyroidism, pseudohypoparathyroidism

- familial hypocalciuric hypercalcemia

- hypophosphoremia sustained by genetic causes or secondary to other causes.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No intervention are provided


Locations

Country Name City State
Italy Azienda USL of Modena Modena

Sponsors (1)

Lead Sponsor Collaborator
Azienda USL Modena

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Calcium Assay performed at the moment of diagnosis Enrollment time
Secondary Phosphorus Assay performed at the moment of diagnosis Enrollment time
Secondary Parathormone Assay performed at the moment of diagnosis Enrollment time
Secondary Creatinine Assay performed at the moment of diagnosis Enrollment time
Secondary Albumine Assay performed at the moment of diagnosis Enrollment time
Secondary Vitamin D Assay performed at the moment of diagnosis Enrollment time
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