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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03132831
Other study ID # RNI2016-34 Pr Mertl
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 1, 2018
Est. completion date December 1, 2018

Study information

Verified date May 2023
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Reducing the length of stay (LOS) after primary arthroplasty is a relatively new target that arouses the attention of orthopedic surgeons in order to return home early through the fast recovery protocols but this goal is also wanted in public health for the sake of overall decline health spending in public costs.


Description:

Reducing the length of stay (LOS) after primary arthroplasty is a relatively new target that arouses the attention of orthopedic surgeons in order to return home early through the fast recovery protocols but this goal is also wanted in public health for the sake of overall decline health spending in public costs. Reducing the LOS after primary hip arthroplasty and knee is studied through many publications that found an LOS influenced by the own medical factors of patients (ref) However, no study to our knowledge research the influence of the operative day and the LOS. For historical reasons, the organization of care is modified on the weekend (Saturday and Sunday) in particular by reducing the caregiver and also the lack of physical therapist to make the early postoperative get up (D0 or D1). The hypothesis is that a patient operated the friday did not have the same care the first 48 hours that a patient who had surgery at the beggening of the week and that his recovery was therefore extended. The investigator can also suppose that LOS was shorter for patients returning home for those who were transferred to a rehabilitation center or other structure. The results will be adjusted according to the literature data on the age more than 80 years, sex, diabetes, cardiovascular diseases, respiratory diseases.


Recruitment information / eligibility

Status Completed
Enrollment 1663
Est. completion date December 1, 2018
Est. primary completion date December 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All major patients operated at the University Hospital of Amiens between 1 January 2015 and 31 December 2016 for primary hip and knee arthroplasty Exclusion Criteria: - All patients undergoing surgery for hip or knee surgery (reoperation). - All patients undergoing total arthroplasty on fracture of the femoral neck from all causes.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Determine the DMS of the Total Hip Prosthesis of the University Hospital of Amiens (PTH) and the Total Knee Prosthesis (PTG)
To determine the DMS of the orthopedic department of the Amiens University Hospital after Total Hip Prosthesis (PTH) and First-line Total Knee Prosthesis (PTG) with its confidence interval and to compare it according to the patient's day of operation

Locations

Country Name City State
France CHU Amiens Picardie Amiens Picardie

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Analysis of the average length of stay in total hip and knee arthroplasty (defined as the time in days between in and out of the orthopedic unit for all destinations) Analysis of the average length of stay in total hip and knee arthroplasty (defined as the time in days between in and out of the orthopedic unit for all destinations) 1 year
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