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Completed No phase listed Observational

Hyponatremia Registry for Patients With Euvolemic and Hypervolemic Hyponatremia

ClinicalTrials.gov ID: NCT01240668

Public ClinicalTrials.gov record NCT01240668. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 8:22 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Observational Prospective Registry to Identify Demographic and Clinical Characteristics of Patients Hospitalized With Euvolemic and Hypervolemic Hyponatremia and Assess the Comparative Effectiveness of Available Treatments and the Impact on Resource Utilization

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The registry is a multi-center, prospective, observational study designed to collect data in patients with euvolemic and hypervolemic hyponatremia in the hospital setting in the USA and hyponatremia secondary to syndrome of inappropriate antidiuretic hormone secretion (SIADH) in Europe; patients with hypovolemic hyponatremia will be excluded from the registry. The registry is observational in design, and the registry will collect data on patients with a serum sodium ≤130 mmol/L. Data from the patients' chart will be collected throughout the duration of the hospital, from admission to discharge, and the data will be entered into the case report form (CRF) or into an electronic data capture (EDC) system. These patients will be entered into the registry over the duration of 18 months at community, tertiary, and academic medical centers from diverse multiple regions of the USA and Europe. A patient's treatment will be determined by their caregiver and not by this protocol. Thus, the registry will provide a unique opportunity to evaluate how the patients are managed under real-world management conditions.

Study identification

NCT ID
NCT01240668
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Otsuka America Pharmaceutical
Industry
Enrollment
5,028 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2010 (Type not available)
Primary completion
Jun 2013 (Actual)
Completion
Aug 2013 (Actual)
Last update posted
May 15, 2015

2010 – 2013

United States locations

U.S. sites
72
U.S. states
23
U.S. cities
61
Facility City State ZIP Site status
North America Research Institute Azusa California — —
Chrishard Medical Group Inglewood California — —
UCLA Los Angeles California — —
Regional Cardiology Associates Sacramento California — —
Portercare Adventist Health System Denver Colorado — —
Georgetown University Hospital Washington D.C. District of Columbia — —
Memorial Healthcare System Hollywood Florida — —
Jacksonville Cardiovascular Center Jacksonville Florida 32216 —
Kidney & HTN Specialists of Miami Miami Florida — —
Naples Community Hospital Naples Florida — —
Florida Hospital Orlando Florida — —
Coastal Nephrology Associates Research Port Charlotte Florida — —
St. Joseph's Hospital of Atlanta Atlanta Georgia — —
Joseph M Still Research Foundation, Inc Augusta Georgia 30909 —
Northwestern Memorial Hospital Chicago Illinois — —
Rush University Medical Center Chicago Illinois — —
Loyola University Medical Center Maywood Illinois — —
Research Integrity, LLC Owensboro Kentucky — —
Ochsner Multi-Organ Transplant Center New Orleans Louisiana — —
Detroit Medical Center Detroit Michigan — —
Detroit Receiving Hospital Detroit Michigan — —
Central Michigan Community Hospital Mount Pleasant Michigan — —
Providence Park Hospital Novi Michigan — —
Northern Michigan Hospital Petoskey Michigan — —
Covenant Heart Specialists Saginaw Michigan — —
Hennepin County Medical Center Minneapolis Minnesota — —
Saint Louis University Hosptial St Louis Missouri — —
Creighton University Omaha Nebraska — —
University Medical Center of Southern Nevada Las Vegas Nevada 89106 —
Hackensack University Medical Center Hackensack New Jersey — —
Hypertenstion and Renal Group Livingston New Jersey — —
St Joseph's Regional Medical Center Paterson New Jersey — —
Princeton Hypertension Nephrology Associates Princeton Junction New Jersey — —
Tufts New England Medical Center Boston New York — —
Buffalo General Hospital Buffalo New York — —
The Jamaica Hospital Medical Center Jamaica New York — —
Winthrop-University Hospital Mineola New York — —
Beth Israel Medical Center-Petrie Division New York New York — —
Center for Liver Disease and Transplantation New York New York — —
Mount Sinai School of Medicine New York New York — —
NYU New York New York — —
Rochester General Rochester New York — —
University of Rochester Rochester New York — —
St Catherine of Siena Medical Center Smithtown New York — —
Jack D. Weiler Hospital The Bronx New York — —
Montefiore Medical Center The Bronx New York — —
Duke University Durham North Carolina — —
Piedmont Respiratory Research Greensboro North Carolina — —
Mercy Hospital Canton Ohio — —
University of Cinncinati Cincinnati Ohio — —
Metrohealth Medical Center Cleveland Ohio 44109 —
Cleveland Clinic Cleveland Ohio — —
Mercy Hospital Fairfield Fairfield Ohio 45104 —
Kettering Health Network Kettering Ohio — —
Kidney Care Specialists Kettering Ohio — —
St Elizabeth Health Center Youngstown Ohio — —
NE Clinical Research Center Bethlehem Pennsylvania — —
Delaware County Memorial Hospital Drexel Hill Pennsylvania — —
Heart Specialists of Lancaster PC Eprata Pennsylvania — —
Laurel Health System Mansfield Pennsylvania — —
UPMC Center for Liver Disease Pittsburgh Pennsylvania — —
SC Nephrology & Hypertension Ctr Orangeburg South Carolina — —
Southeast Renal Research Institute Chattanooga Tennessee — —
Saint Thomas Hospital Nashville Tennessee — —
Baylor University Medical Center Dallas Texas — —
Cardiopulmonary Research Science & Technology Institute Dallas Texas — —
Baptist Hospital Downtown San Antonio Texas 78205 —
Renal Associates, PA San Antonio Texas — —
Clinical Research and Consulting Centter Fairfax Virginia — —
Sentara Norfolk General Hospital Norfolk Virginia — —
Virginia Commonwealth University Medical Center Richmond Virginia — —
CAMC Institute Inc. Charleston West Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01240668, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 15, 2015 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01240668 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →