Institutional Registry of Hyponatremia (Hyponatremia)
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|ClinicalTrials.gov Identifier: NCT01370473|
Recruitment Status : Completed
First Posted : June 10, 2011
Last Update Posted : August 13, 2019
The purpose of this study is to create an institutional and population-based registry of Hyponatremia with a prospective survey based on epidemiological data, risk factors, diagnosis, prognosis, treatment, monitoring and survival.
This study will also describe the occurrence of hyponatremia in the population of HIBA in the Central Hospital, as well as the characteristics of clinical presentation, evolution and predisposing factors of hyponatremia.
|Condition or disease|
|Study Type :||Observational|
|Actual Enrollment :||2000 participants|
|Official Title:||Institutional Registry of Hyponatremia|
|Study Start Date :||December 2006|
|Actual Primary Completion Date :||May 2014|
|Actual Study Completion Date :||May 2014|
- clinical features [ Time Frame: feature clinics are evaluated during the acute episode and mortality were measured in the acute episode and in the semiannual monitoring by telephone ]Signs and symptoms Hospital Length of Stay Mortality Therapy
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01370473
|Hospital Italiano de Buenos Aires|
|Buenos Aires, Argentina, 1199|
|Principal Investigator:||Diego H Giunta, MD||Hospital Italiano de Buenos Aires|