NCT01910233

Brief Summary

This is a prospective registry of patients presenting with acute dyspnea to the emergency department of the city hospital in Nuremberg. There is evidence that acute dyspnea is associated with a mortality rate of 10%, however acute dyspnea is not perceived as a life-threatening condition, both in public and in health care providers. Our aim is to describe the patient collective concerning their demographics, baseline characteristics, type of referral and disposition, medical care processes and prognosis. Secondly, we want to evaluate if the subjective risk assessment of emergency department personnel matches with objective risk stratification tools and the actual outcome of the studied patients.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
947

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2013

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

May 1, 2013

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

July 25, 2013

Completed
4 days until next milestone

First Posted

Study publicly available on registry

July 29, 2013

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2015

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2015

Completed
Last Updated

April 1, 2016

Status Verified

March 1, 2016

Enrollment Period

2 years

First QC Date

July 25, 2013

Last Update Submit

March 31, 2016

Conditions

Keywords

dyspnearegistrybaseline characteristicsmortalityrisk assessmentemergency department

Outcome Measures

Primary Outcomes (1)

  • all cause mortality

    6 months

Secondary Outcomes (3)

  • demographics and baseline characteristics

    1 month

  • medical care processes

    1 day

  • subjective and objective risk assessment

    1 month

Study Arms (1)

adult patients with acute dyspnea in ED

Eligibility Criteria

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

Patients presenting to the emergency department of the city hospital Nuremberg

You may qualify if:

  • expression of acute dyspnea in the emergency department

You may not qualify if:

  • age \< 18 years

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Emergency and Critical Care Medicine, City Hospital Nuremberg

Nuremberg, Bavaria, 90471, Germany

Location

MeSH Terms

Conditions

DyspneaHeart FailurePulmonary Disease, Chronic ObstructiveEmergencies

Condition Hierarchy (Ancestors)

Respiration DisordersRespiratory Tract DiseasesSigns and Symptoms, RespiratorySigns and SymptomsPathological Conditions, Signs and SymptomsHeart DiseasesCardiovascular DiseasesLung Diseases, ObstructiveLung DiseasesChronic DiseaseDisease AttributesPathologic Processes

Study Officials

  • Michael Christ, Prof.

    Klinikum Nürnberg

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
6 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof. Dr. med. Michael Christ

Study Record Dates

First Submitted

July 25, 2013

First Posted

July 29, 2013

Study Start

May 1, 2013

Primary Completion

May 1, 2015

Study Completion

December 1, 2015

Last Updated

April 1, 2016

Record last verified: 2016-03

Locations