NCT07276061

Brief Summary

Outpatient TKA is a controversial topic due to concerns about its safety as an outpatient procedure, and remains a marginal procedure. Advances in enhanced postoperative rehabilitation protocols, coupled with advances in minimally invasive surgery, have made it possible to operate on an increasing number of patients on an outpatient basis. However, there are no studies in the literature analyzing functional recovery after outpatient TKA in France. The objective of this study was to compare postoperative recovery, assessed by the QoR-15F score, in patients undergoing outpatient TKA compared to those undergoing a conventional hospitalization.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
440

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Mar 2024

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 11, 2024

Completed
1 year until next milestone

First Submitted

Initial submission to the registry

March 25, 2025

Completed
9 months until next milestone

First Posted

Study publicly available on registry

December 10, 2025

Completed
21 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

December 10, 2025

Status Verified

March 1, 2025

Enrollment Period

1.8 years

First QC Date

March 25, 2025

Last Update Submit

December 8, 2025

Conditions

Knee Arthroscopy

Keywords

knee arthroscopy

Outcome Measures

Primary Outcomes (1)

  • QoR-15F score

    at Day 1,Day 3, Day 14 and Day 28 post-operative

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Male or female, 18 years of age or older (no upper age limit) undergoing scheduled unilateral total knee replacement surgery between January 1, 2020 and June 30, 2023 at the Strasbourg University Hospitals

You may qualify if:

  • Male or female, 18 years of age or older (no upper age limit)
  • Undergoing scheduled unilateral total knee replacement surgery between January 1, 2020 and June 30, 2023 at the Strasbourg University Hospitals
  • Assessed using the QoR-15F score

You may not qualify if:

  • Subject who has expressed opposition to the reuse of their data for scientific research purposes.
  • Revision, emergency, oncological, bilateral, or septic surgery.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Service d'Anesthésie - Réanimation & Médecine Périopératoire - CHU de Strasbourg - France

Strasbourg, 67091, France

RECRUITING

Central Study Contacts

Eric NOLL, MD, PhD

CONTACT

33 3 88 12 70 76eric.noll@chru-strasbourg.fr

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 25, 2025

First Posted

December 10, 2025

Study Start

March 11, 2024

Primary Completion

December 31, 2025

Study Completion

December 31, 2025

Last Updated

December 10, 2025

Record last verified: 2025-03

Locations

FR(1)