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| Sponsor: | Scios, Inc. |
|---|---|
| Information provided by: | Scios, Inc. |
| ClinicalTrials.gov Identifier: | NCT00366639 |
Purpose
The purpose of the ADHERE study is to develop a multi-center, observational, open-label registry of the management strategies of patients treated in the hospital for acute Heart Failure in the United States.
| Condition | Intervention |
|---|---|
|
Heart Failure, Congestive Heart Decompensation |
Other: Acute Decompensated Heart Failure |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | ADHERE Core III - Acute Decompensated Heart Failure Registry |
| Enrollment: | 24118 |
| Study Start Date: | October 2001 |
| Study Completion Date: | February 2006 |
| Groups/Cohorts | Assigned Interventions |
|---|---|
| 001 |
Other: Acute Decompensated Heart Failure
Treatment & outcomes during hospital admission for Acute DHF
|
The objective is to compile a clinical database on the strategy for the medical management of patients hospitalized with acute Heart Failure (HF). Through the use of the information collected from acute care hospitals across the United States the following information may be coming out of this study: 1) Assist hospitals in evaluating and improving quality of care for patients with acute HF by tracking quality indicators and providing benchmark data reports; 2) Describe the demographic and clinical characteristics of patients who are hospitalized with acute HF; 3) Characterize the initial emergency department evaluation and subsequent inpatient management of patients hospitalized with acute HF; 4) Identify patient characteristics and medical care practices associated with improved health outcomes in those hospitalized with acute HF; 5) Characterize trends and changes over time in the management of acute HF; 6) Offer surveillance of adherence to practice guidelines as these emerge for the inpatient management of acute HF. Observational Study - No investigational drug administered
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
All consecutive adult patients admitted to an acute care hospital and treated actively for acute HF, where acute HF is defined clinically as a new onset with HF decompensation
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Responsible Party: | Scios ( Sr. Director, Clinical Team Leader ) |
| Study ID Numbers: | CR005194 |
| Study First Received: | August 18, 2006 |
| Last Updated: | October 29, 2009 |
| ClinicalTrials.gov Identifier: | NCT00366639 History of Changes |
| Health Authority: | United States: Institutional Review Board |
|
Heart failure, congestive Heart decompensation |
|
Heart Failure Heart Diseases Cardiovascular Diseases |