Safety of Total Knee Replacement Surgery Before and After the Implementation of Enhanced Recovery Program
NCT ID: NCT05028426
Last Updated: 2022-07-07
Study Results
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View full resultsBasic Information
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COMPLETED
455 participants
OBSERVATIONAL
2015-01-31
2019-10-31
Brief Summary
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Detailed Description
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At la Rochelle hospital, the decision to take the step happened at the end of 2016. It was proposed by a young surgeon that have been trained on this new approach during his studies and who convinced the head of the surgery department of the benefits for the patients, the healthcare workers, and the institution. The transition took place in two stages, first operative and postoperative techniques were modified, and then preoperative education and counselling were added.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Traditional method of care
Patients managed according to the traditional care protocol without an enhanced recovery program
No interventions assigned to this group
Some elements of a fast-track program
operative and postoperative techniques were modified according to a fast-track program
Enhanced recovery program
Enhanced recovery programs are a multimodal approach to optimize patients' physiological and psychological states in the preoperative, intraoperative and postoperative care domains.
Full enhanced recovery program
Patients were managed in an enhanced recovery program (elements of the previous fast-track program were modified and preoperative education was added)
Enhanced recovery program
Enhanced recovery programs are a multimodal approach to optimize patients' physiological and psychological states in the preoperative, intraoperative and postoperative care domains.
Interventions
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Enhanced recovery program
Enhanced recovery programs are a multimodal approach to optimize patients' physiological and psychological states in the preoperative, intraoperative and postoperative care domains.
Eligibility Criteria
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Inclusion Criteria
* unilateral arthroplasty
* a known address for mailing the study information letter
Exclusion Criteria
* patients who refused to the use of their data
18 Years
ALL
No
Sponsors
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Groupe Hospitalier de la Rochelle Ré Aunis
OTHER
Responsible Party
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Principal Investigators
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Vivien Fontaine, MD
Role: STUDY_DIRECTOR
Groupe Hospitalier La Rochelle Ré Aunis
Locations
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Groupe Hospitalier la Rochelle Ré Aunis
La Rochelle, , France
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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2018/P01/266
Identifier Type: -
Identifier Source: org_study_id
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