NCT01081925

Brief Summary

The purpose of the study is to recognize main causes of acute decompensation of chronic congestive heart failure.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Feb 2010

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2010

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

March 4, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

March 5, 2010

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2012

Completed
Last Updated

March 5, 2010

Status Verified

February 1, 2010

Enrollment Period

2 years

First QC Date

March 4, 2010

Last Update Submit

March 4, 2010

Conditions

Congestive Heart Failure

Keywords

Congestive Heart FailureCardiac Failure

Study Arms (1)

Congestive heart failure

Patients suffering from sudden worsening of congestive heart failure

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients suffering from sudden worsening of congestive heart failure, who are examined at the Emergency department or admitted to University Hospital

You may qualify if:

  • able to provide informed consent
  • aged 19 years or more
  • history of heart failure of at least one month
  • examined or hospitalized for acute dyspnea at rest or with minimal exertion
  • clinical signs of fluid overload defined as at least one of following:
  • rales
  • jugular venous distension
  • peripheral edema
  • pulmonary congestion on X-ray
  • NT-proBNP above 210 pmo/l

You may not qualify if:

  • none

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital Hradec Kralove

Hradec Králové, 50005, Czechia

RECRUITING

MeSH Terms

Conditions

Heart Failure

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Officials

  • Radek Pelouch, MD

    University Hospital Hradec Kralove

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Radek Pelouch, MD

CONTACT

00420495834740pelouch@centrum.cz

Jiri Ceral, MD

CONTACT

00420495832652ceral@seznam.cz

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER

Study Record Dates

First Submitted

March 4, 2010

First Posted

March 5, 2010

Study Start

February 1, 2010

Primary Completion

February 1, 2012

Study Completion

February 1, 2012

Last Updated

March 5, 2010

Record last verified: 2010-02

Locations

CZ(1)