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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02437058
Other study ID # 2011111045
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2011
Est. completion date May 2015

Study information

Verified date July 2020
Source Hospital Galdakao-Usansolo
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The scales measuring the severity of acute decompensate heart failure (ADHF) in emergency departments have not achieved an adequate discriminative ability for decision making. Objectives: 1) Identify baseline variables, and evolutionary variables that may provide a good predictive ability of the model.2) Create and validate clinical predictive rules of mortality during admission/a week after ED visit in those discharged from ED, 30 and 60 days after ED visit as well as identify predicitive factors of short-term readmission (90 days)Design: Prospective cohort study. The sociodemographics and clinical variables will be collected from emergency medical records to identify predictors. Outcome variables and evolution of variables will be collected from hospital medical records / ambulatory during admission and up to 90 days after the episode of ADHF. Baseline predictors and evolutionary variables will be identified through logistic regression models using 60% of the final sample. The models that best fit will be applied in 40% of the sample to assess the predictive validity of this scale.


Recruitment information / eligibility

Status Completed
Enrollment 1854
Est. completion date May 2015
Est. primary completion date April 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- They were diagnosed as heart failure) HF is defined, clinically, as a syndrome in which patients have typical symptoms (e.g.breathlessness, ankle swelling, and fatigue) and signs (e.g. elevated jugular venous pressure, pulmonary crackles, and displaced apex beat) resulting from an abnormality of cardiac structure or function.(8) We included the following presentation of acute heart failure (AHF) at ED: acute decompensated heart failure, hypertensive acute heart failure, pulmonary oedema, cardiogenic shock, and high output failure. (9;10)

Exclusion Criteria:

- Patients whose main diagnosis in the ER is different than acute heart failure and those not wishing to participate in the study or signing the informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
preidictive model


Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
Hospital Galdakao-Usansolo Hospital de Basurto, Hospital Donostia

Outcome

Type Measure Description Time frame Safety issue
Primary Poor evolution 3 months
Secondary readmission 3 months
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