Auto-administered Questionnaire by Screening of Disorder of the Haemostasis in Preoperative

Completed

• Conditions: Preoperative Assessment of Hemostasis

• Registration Number: NCT02886117
• Lead Sponsor: University Hospital, Brest

Brief Summary

The main objective of this study is to determine the capacity of a questionnaire to predict a normal balance sheet of haemostasis.

Detailed Description

Recent recommendations formalized by experts of the French society of anaesthesiology on systematic pre-interventional examinations recommend assessing the risk of bleeding from personal and family history of bleeding diathesis and after physical examination . They recommend not to prescribe a systematic hemostasis laboratory tests in patients with a history and physical examination do not suspect a disorder of hemostasis.

However, there is currently no validated questionnaire in the general population to assess the preoperative bleeding risk allowing a reliable assessment of the personal and family bleeding diathesis.

The establishment of a structured questionnaire, the patient could filled before surgery consultation to guide the possible prescription of a balance sheet, could meet the new recommendations.

It seems therefore important to establish this type of questionnaire in order to optimize the operation of the structure, and to limit the requirements of routine hemostasis balance sheets. To do this, the investigator wants to carry out a preliminary study to ensure the interest of the established questionnaire.

The questionnaire assessed in this study is drawn from existing specialized questionnaires, the description of hemostasis disorders described factor for deficits from the doctor in charge of hemophilia expertise center and expertise of a psychologist, to refine best.

Study Timeline

• Study Start: 2014-10
• Primary Completion: 2015-08
• Study Completion: 2015-08
• Status Verified: 2016-08
• Study First Submitted: 2016-08-29
• Study First Submitted QC: 2016-08-31
• Last Update Submitted: 2016-08-31
• Study First Posted: 2016-09-01
• Last Update Posted: 2016-09-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 2511

Inclusion Criteria

• All adults addressed in programmed anesthesia consultation, regardless of whether surgery and consultation site

Exclusion Criteria

• Patients minors
• Physical or mental disability in Patient to agree and complete the questionnaire
• Major patients undergoing a protective measure
• Refusal of participation

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
hemostasis tests (normal or abnormal)	Inclusion

Trial Locations

Locations (1)

CHRU de Brest; 🇫🇷 Brest, France