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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02932982
Other study ID # 29BRC16.0143
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date October 21, 2016
Est. completion date May 9, 2018

Study information

Verified date November 2018
Source University Hospital, Brest
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Dyspnea and chest pain represent 1.5% of general practice consultations. They may be a sign of many diseases, potentially serious. The concept of Gut Feelings brings a sense of alarm and reinsurance. The sense of alarm reflects a sense of mistrust about the patient's clinical situation, in the absence of objective argument. The sense of reinsurance reflects a sense of confidence about the patient's situation, in the absence of objective argument. Gut Feelings plays a key role in the diagnostic reasoning in general practice. A questionnaire measuring the Gut Feelings was validated in French after a linguistic validation procedure.


Description:

Dyspnea and chest pain represent 1.5% of general practice consultations. They may be a sign of many diseases, potentially serious. The concept of Gut Feelings brings a sense of alarm and reinsurance. The sense of alarm reflects a sense of mistrust about the patient's clinical situation, in the absence of objective argument. The sense of reinsurance reflects a sense of confidence about the patient's situation, in the absence of objective argument. Gut Feelings plays a key role in the diagnostic reasoning in general practice. A questionnaire measuring the Gut Feelings was validated in French after a linguistic validation procedure.

The objective of the research is to calculate the precision of the sense of alarm the general practitioner facing a consultant for chest pain or dyspnea and patient


Recruitment information / eligibility

Status Terminated
Enrollment 241
Est. completion date May 9, 2018
Est. primary completion date May 9, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients between 18 and 80 years

- Patients consulting on primary care for chest pain or dyspnea

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France ABALAIN-VOREUX Aurélie Brest
France SIMON Benjamin Brest
France AUFFRET Jean François Camaret Sur Mer
France POINOT Anne Guerlesquin
France LE GOFF Delphine La Forêt Landerneau
France BEURTON-COURAUD Lucas Pleyben
France LE DUFF Nicolas Ploudalmezeau
France BODIN Bénédicte Plounéour Trez
France CAM Françoise Plouzané
France LOSQUIN André Pont l'Abbé
France MAHE Gwénaëlle Saint Nicolas du Pelem

Sponsors (3)

Lead Sponsor Collaborator
University Hospital, Brest Ecole doctorale de Bretagne en biologie de santé, University of Anvers

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary calculate the accuracy of the sense of alarm the general practitioner face a patient consultant for chest pain or dyspnea. Questionary 4 weeks
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