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Aspirin Thromboprophylaxis After First-line Total Hip and Knee Replacement

Aspirin Thromboprophylaxis After First-line Total Hip and Knee Replacement. Comparison With Baseline Low Molecular Weight Heparin Prophylaxis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05128214
Acronym
TBP-ASPIR
Enrollment
200
Registered
2021-11-19
Start date
2021-06-18
Completion date
2021-12-31
Last updated
2021-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip and Knee Prosthesis Implantation

Keywords

Hip prosthesis implantation, Knee prosthesis implantation, Aspirin thromboprophylaxis, Heparin prophylaxis, Thromboembolic complications, Bleeding complications

Brief summary

Annually, more than 100,000 total hip prostheses (THA) and more than 100,000 total knee prostheses (TKA) are implanted for osteoarthritis in France, and these figures are set to increase significantly in the future as in all industrialized countries. . Venous thrombosis is a potentially serious complication after PTH and PTG, justifying various prophylactic measures. In France, aggressive prophylaxis with low molecular weight heparin (LMWH) or direct oral anticoagulants (DOA) was until recently recommended, because this drug is considered to be the most effective, at the cost of a bleeding risk implicitly assumed but often poorly. evaluated. A recent publication suggests that the risk of bleeding is currently greater than the risk of a thromboembolic event. More recently, foreign or international recommendations have broadened the range of these recommendations, notably by introducing aspirin as a possible prophylactic agent. While this molecule is potentially less effective than LMWHs or ADOs, it could decrease the risk of iatrogenic hemorrhage. The introduction of enhanced recovery procedures after surgery (RAAC) could decrease the risk of thrombosis without modifying the risk of bleeding, and thereby improve the cost-benefit ratio of aspirin, justifying its recent inclusion in the current French recommendations when The operated follows such a protocol.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Adult patient (≥ 18 years old); * Patient operated on for a first-line total hip or knee replacement by the principal investigator; * Patient not having expressed his opposition, after information, to the reuse of his data for the purposes of this research.

Exclusion criteria

\- Subject having expressed opposition to participating in the study

Design outcomes

Primary

MeasureTime frame
Study of the postoperative thromboembolic complications after implantation of hip and knee prosthesesFiles analysed retrospectively from July 01, 2016 to December 31, 2020 will be examined]

Countries

France

Contacts

Primary ContactJean-Yves JENNY, MD, PhD
jean-yves.jenny@chru-strasbourg.fr33 3 68 76 52 87
Backup ContactSaïd CHAYER, PhD, HDR
said.chayer@chru-strasbourg.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026