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Total Knee Replacement Under Spinal Anesthesia, Comparison of Postoperative Recovery Versus General Anesthesia

Total Knee Replacement Under Spinal Anesthesia, Comparison of Postoperative Recovery Versus General Anesthesia: A Retrospective Single-Center Observational Comparative Superiority Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07275983
Acronym
PTG-RachiVsAG
Enrollment
500
Registered
2025-12-10
Start date
2024-05-03
Completion date
2025-12-03
Last updated
2025-12-10

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

Conditions

Total Knee Replacement

Keywords

knee, Total Knee Replacement, Spinal Anesthesia

Brief summary

Intraoperative anesthetic management for total knee replacement (TKR) can be performed under general or spinal anesthesia. These two techniques have their own characteristics and may impact postoperative recovery differently. However, there are no studies in the literature analyzing postoperative functional recovery after TKR surgery according to the type of anesthesia. The objective of this study is to compare postoperative recovery, assessed by the QoR-15F score, in patients undergoing TKR under spinal anesthesia versus surgery under general anesthesia.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* Male or female, 18 years of age or older (no upper age limit) * Underwent total knee replacement surgery between January 1, 2020 and June 30, 2023 * Assessed using the QoR-15F score

Exclusion criteria

* Subject (and/or their legal representative, if applicable) who expressed their opposition to the reuse of their data for scientific research purposes. * Revision, emergency, oncological, bilateral, or septic surgery

Design outcomes

Primary

MeasureTime frame
QoR-15F scoreat Day 1, Day3, Day 14, and Day 28 postoperatively

Countries

France

Contacts

Primary ContactEric NOLL, MD, PhD
eric.noll@chru-strasbourg.fr33 3 88 12 70 76

Outcome results

None listed

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