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Management of Patients on Long Term Anticoagulation Therapy Undergoing a Primary Total Hip of Knee Replacement (ADELC)

A

Association pour le Développement et l'Enseignement de la Chirurgie Réparatrice et Orthopédique

Status

Unknown

Conditions

Postoperative Complications

Treatments

Drug: anticoagulation

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

It is a multicenter, prospective, observational study of standard care. This study analyses the care of patients on long term effective anticoagulation therapy (ADELC) during a primary hip or knee arthroplasty.

The objectives of the study are to:

  1. Identify clinical practices set up for patient care
  2. Assess the type and the frequency of perioperative complications
  3. Look for factors, related to patients or treatments, associated with the occurrence of these complications.

The main objective is to estimate the risks, adjusted and not, of postoperative complications associated to a long term anticoagulation by comparing patients under anticoagulation to a control group of patients having the same interventions but who are not under anticoagulation.

Enrollment

600 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult ≥ 18 years
  • Programmed for primary hip or knee arthroplasty.
  • Effective dose of anticoagulant drugs intake for more than 1 month with the intention to resume it after the intervention for ADELC cohort; no effective dose of anticoagulant drugs intake for the control cohort.

Exclusion criteria

  • Patient non opposition

Trial design

600 participants in 2 patient groups

ADELC
Description:
Cohort of patients on long term anticoagulation and undergoing a primary hip or knee replacement.
Treatment:
Drug: anticoagulation
CONTROL
Description:
Cohort of patients not on long term anticoagulation and undergoing a primary hip or knee replacement.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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