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Real-world retrospective study of incidence of and risk factors for moderate-to-severe pain after knee arthroplasty

Real-world retrospective study of incidence of and risk factors for moderate-to-severe pain after knee arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20190624001
Enrollment
Unknown
Registered
2019-06-24
Start date
2017-01-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

knee arthroplasty Real&#45

Interventions

All patients were divided into two main groups according to the maximum NRS score reported in the first postoperative day. Patients with a maximum NRS score of > 4 out of 10 during the first 12 hours
24 hours after surgery were allocated to the moderate&#45
severe pain group&#44
whereas those with a maximum NRS score of 4 at only one occasion during the first 24 hours after surgery were allocated to the mild pain group. Factors associated with moderate&#45
severe postoperative pain were analyzed.
Screening
severe pain (NRS>4)

Sponsors

None listed

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All the consecutive patients who underwent unicompartmental knee arthroplasty (UKA) or total knee arthroplasty (TKA) were eligible for inclusion.

Exclusion criteria

Exclusion criteria: Patients were excluded, if they underwent simultaneous bilateral knee arthroplasty or revision knee arthroplasty, underwent knee arthroplasty due to having bone tumor, admitted to the intensive care unit (ICU) after surgery, or had incomplete electronic medical records.

Design outcomes

Primary

MeasureTime frame
incidence of severe and moderate pain the first 24 hours after surgery the numerical rating scale

Secondary

MeasureTime frame
risk factors for moderate-to-severe pain the first 24 hours after surgery the numerical rating scale

Countries

Thailand

Contacts

Public ContactArissara Iamaroon

Mahidol University

arisa21@gmail.com+6624197978

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026