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Clinical Trials/NCT02886117
NCT02886117
Completed
Not Applicable

Creation and Evaluation of a Auto-administered Questionnaire by Screening of Disorder of the Haemostasis in Preoperative

University Hospital, Brest1 site in 1 country2,511 target enrollmentOctober 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Preoperative Assessment of Hemostasis
Sponsor
University Hospital, Brest
Enrollment
2511
Locations
1
Primary Endpoint
hemostasis tests (normal or abnormal)
Status
Completed
Last Updated
9 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 2014
End Date
August 2015
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

hemostasis tests (normal or abnormal)

Time Frame: Inclusion

Study Sites (1)

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