Skip to content

Fast-track Rehabilitation After Total Knee or Hip Arthroplasty

Fast-track Rehabilitation After Total Knee or Hip Arthroplasty: an Observational Prospective Case-control Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03035435
Enrollment
58
Registered
2017-01-30
Start date
2016-01-31
Completion date
2016-09-30
Last updated
2017-07-26

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

Conditions

Hip Arthroplasty, Knee Arthroplasty

Keywords

fast-track rehabilitation, fast-track surgery

Brief summary

In the last years, a lot of surgical fast track programs (SFTP) have been created and developed. This is due to the steady growing number of interventions on knee and hip; after the surgical treatment, a period of physical rehabilitation (PR) is established to be useful and effective, it usually takes 2-3 weeks. The recovery of strength, range of motion (ROM), independence, the reduction of pain and disability are the aims of PR. With the SFTP and a specific rehabilitation program named fast track rehabilitation (FTR) these times can be reduced. First of all because the length of stay (LOS) it's also caused by organizational problems of the hospitals, not only for the factors related to the patient. It's already been demonstrated that an early mobilization decreases the risk of thromboembolic complications and of pain, furthermore an early rehabilitation increase the patient autonomy and reduces the lost of residual abilities. Moreover a PR program studied for fast track patient will reduce minimum by a 50% the LOS in hospital, decreasing so the sanitary efforts that are always a problem for all the countries. The aim of this study is therefore to propose a fast track rehabilitation program based on an 8 days program for hip and knee arthroplasty being operated with an SFTP.

Interventions

Sponsors

Fondazione Don Carlo Gnocchi Onlus
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* adult people (\>18 years), both sex, admitted for elective total knee or hip arthroplasty, with a clinical stability (Hb\>9 g/l).

Exclusion criteria

* the presence of pain measured with NRS (NRS\>4) * rheumatoid arthritis, past surgery * cancer * neurological and psychiatric disorders * dementia with Minimental Test\<24 * pregnancy * participation in the other clinical studies.

Design outcomes

Primary

MeasureTime frame
International Knee Society ScoreChange from Baseline fast-track rehabilitation at 8th and 15th day
Merle D'Aubigne' scaleChange from Baseline fast-track rehabilitation at 8th and 15th day

Secondary

MeasureTime frame
Barthel IndexChange from Baseline fast-track rehabilitation at 8th and 15th day

Outcome results

None listed

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