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Completed

NCT Number: NCT02886117

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

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHRU de Brest

Brest, 29609, France

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. hemostasis tests (normal or abnormal)

    Time frame: Inclusion

Sponsors and collaborators

Lead sponsor

University Hospital, Brest

Other

Registry information

Official study title

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

Acronym: HEMOSTASE

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Sep 1, 2016
Registry last updated
Sep 1, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.