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NCT05286671 Clinical Trial

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

Femoral Neck Fractures Clinical Trial

— ANTICOGER  

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05286671
Other study ID # LOCAL/2022/CC-01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 1, 2022
Est. completion date March 11, 2022

Study information
Verified date March 2022
Source Centre Hospitalier Universitaire de Nimes
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date March 11, 2022
Est. primary completion date March 11, 2022
Accepts healthy volunteers No
Gender All
Age group 75 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Chu Nimes Nimes

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nimes

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Rate of compliance with the recommendations for direct oral anticoagulants (DOAC).. Rate of compliance with the french working group on perioperative haemostasis (GIHP) recommendations for DOACrecommendations for DOA. Day 0
Primary Rate of compliance with the recommendations for vitamin K antagonists (VKA). Rate of compliance with the french health authority (HAS) recommendations for VKA Day 0
Secondary Number of pharmaceutical interventions Number of pharmaceutical interventions regarding anticoagulant prescriptions Day 0
Secondary description of pharmaceutical interventions description of pharmaceutical interventions Day 0
Secondary Evaluation of the morbi-mortality Mortality, re-hospitalizations at 30 days, characterization of bleeding complications, characterization of thrombotic complications Day 0
Secondary Description of the evolution of the plasma dosage of DOAC and the international normalized ratio (INR) and analysis of the operative delay Value of preoperative DOAC plasma dosage, value of INR dosage pre- and post-op, analysis of the operative delay Day 0
Secondary description of the population age, weight, height, body mass index, comorbidities Day 0
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