Polymorphisms of the Thiazide's Receptor Gene SLC12A3 and Development of Hyponatremia

NCT ID: NCT01346891

Last Updated: 2011-07-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-07-31

Brief Summary

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The purpose of this study is to detect if there are any differences in the coding region of SLC12A3 gene in individuals who have had hyponatremia associated to the use of thiazides, and those thiazides consumers without hyponatremia that have demonstrated good tolerance to the drug.

Detailed Description

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This is a Case Control study to compare the coding region of SLC12A3 gene in individuals who have had hyponatremia associated to the use of thiazides, and those thiazides consumers without hyponatremia that have demonstrated good tolerance to the drug.

Conditions

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Thiazide Diuretics Induced Hyponatremia

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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Hyponatremia Group (Cases)

Patients over 21 years old, with confirmed antecedent of thiazide-induced hyponatremia who required hospitalization with a serum sodium concentration lower than 125 meq/L.

No interventions assigned to this group

Good Thiazide Tolerance (Controls)

Patients over 21 years old, who have consumed thiazide diuretics for more than 2 years, with a serum sodium concentration persistently over 135 meq/L.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

1. Patients older than 21 years, belonging to one of the following groups:

1. Patients who have had Thiazide induced hyponatremia with serum sodium lower than 125 meq/L included in the Institutional Registry of Hyponatremia (Cases)
2. Patients with good tolerance to chronic treatment with Thiazides tha never had associated hyponatremia (Controls)
2. Patients with normal serum sodium measurements before the start of the Thiazides

Exclusion Criteria

1. Refusal to participate or to the informed consent process
2. Unclear cause of hyponatremia, or other hyponatremia cause concomitant to Thiazide diuretics
3. Patients related to other individuals already included in the study
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sociedad Argentina de Hipertension Arterial (SAHA)

OTHER

Sponsor Role collaborator

Hospital Italiano de Buenos Aires

OTHER

Sponsor Role lead

Responsible Party

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Hospital Italiano de Buenos Aires

Principal Investigators

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Diego H Giunta, MD

Role: PRINCIPAL_INVESTIGATOR

Hospital Italiano de Buenos Aires

Locations

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Hospital Italiano de Buenos Aires

Capital Federal, Buenos Aires F.D., Argentina

Site Status

Countries

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Argentina

Other Identifiers

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1579

Identifier Type: -

Identifier Source: org_study_id

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