ANTICOGER: Evaluation of Perioperative Management of Curative Anticoagulants in the Geriatric Perioperative Unit in Patient Hospitalized for Femoral Neck Fracture.

Sponsor
Centre Hospitalier Universitaire de Nīmes (Other)
Overall Status
Completed
CT.gov ID
NCT05286671
Collaborator
(none)
30
1
1.2
24

Study Details

Study Description

Brief Summary

Pilot study to evaluate the management of curative anticoagulant prescriptions pre- and postoperatively in elderly patients hospitalized for femoral neck fracture.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    30 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Evaluation of Perioperative Management of Curative Anticoagulants in the Geriatric Perioperative Unit in Patient Hospitalized for Femoral Neck Fracture.
    Actual Study Start Date :
    Feb 1, 2022
    Actual Primary Completion Date :
    Mar 11, 2022
    Actual Study Completion Date :
    Mar 11, 2022

    Outcome Measures

    Primary Outcome Measures

    1. Rate of compliance with the recommendations for direct oral anticoagulants (DOAC).. [Day 0]

      Rate of compliance with the french working group on perioperative haemostasis (GIHP) recommendations for DOACrecommendations for DOA.

    2. Rate of compliance with the recommendations for vitamin K antagonists (VKA). [Day 0]

      Rate of compliance with the french health authority (HAS) recommendations for VKA

    Secondary Outcome Measures

    1. Number of pharmaceutical interventions [Day 0]

      Number of pharmaceutical interventions regarding anticoagulant prescriptions

    2. description of pharmaceutical interventions [Day 0]

      description of pharmaceutical interventions

    3. Evaluation of the morbi-mortality [Day 0]

      Mortality, re-hospitalizations at 30 days, characterization of bleeding complications, characterization of thrombotic complications

    4. Description of the evolution of the plasma dosage of DOAC and the international normalized ratio (INR) and analysis of the operative delay [Day 0]

      Value of preoperative DOAC plasma dosage, value of INR dosage pre- and post-op, analysis of the operative delay

    5. description of the population [Day 0]

      age, weight, height, body mass index, comorbidities

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    75 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patient 75 years or older

    • Hospitalized in the geriatric perioperative unit for a femoral neck fracture between 18/11/2019 and 30/06/2021

    • Treated with a curative anticoagulant at entry

    • Patient enrolled in or receiving a social security plan

    Exclusion Criteria:
    • Orthopedic patient housed in the geriatric perioperative unit

    • Patient who objected to the use of their data

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Chu Nimes Nimes France 30029

    Sponsors and Collaborators

    • Centre Hospitalier Universitaire de Nīmes

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Centre Hospitalier Universitaire de Nīmes
    ClinicalTrials.gov Identifier:
    NCT05286671
    Other Study ID Numbers:
    • LOCAL/2022/CC-01
    First Posted:
    Mar 18, 2022
    Last Update Posted:
    Apr 26, 2022
    Last Verified:
    Mar 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Centre Hospitalier Universitaire de Nīmes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 26, 2022