Clinical Trials Directory

Trials / Completed

CompletedNCT06124170

Improved Pain Management in Knee Osteoarthritis-related Surgeries

Evaluating the Effectiveness of Continuously Improved Pain Management in Knee Osteoarthritis-related Surgeries

Status
Completed
Phase
Study type
Observational
Enrollment
714 (actual)
Sponsor
Peng Liu · Academic / Other
Sex
All
Age
50 Years – 80 Years
Healthy volunteers
Not accepted

Summary

In recent years, pain management coordinated with enhanced recovery after surgery (ERAS) has been widely applied and rapidly developed in orthopedics, showing promising prospects. Since 2016, our hospital has used a series of continuously improved pain management schemes for patients with knee OA who underwent total knee arthroplasty (TKA), unicompartmental knee arthroplasty (UKA), and high tibial osteotomy (HTO). Here, we retrospectively analyze these patients' clinical data to compare the effects of different pain intervention measures during the perioperative period on postoperative pain, functional exercise, hospital stay, and prognosis of the three surgical methods in an attempt to provide a feasible solution for pain management of these patients.

Detailed description

We retrospectively analyzed the clinical data of patients with knee osteoarthritis (OA) who received surgical treatment to provide a feasible solution for perioperative pain management of these patients. The medical records of 714 patients with knee OA who had undergone total knee arthroplasty (n=551), unicompartmental knee arthroplasty (n=92) and high tibial osteotomy (n=71) were retrospectively analyzed and the cases were divided into Groups A, B, and C, according to the continuously optimized pain management. Clinical data including anesthesia grade, surgery time, functional exercise, hospital stay, pain, emotion, complications and prognosis were compared.

Conditions

Interventions

TypeNameDescription
PROCEDUREPreoperative pain managmentpropaganda and education on pain; Preemptive analgesia with celecoxib (200 mg bid) 2 days before surgery
PROCEDUREIntraoperative pain managmentSqueeze to expel blood (tourniquet); Before skin suture, 20 mL 0.5% ropivacaine was given subcutaneously for local infiltration anesthesia;
PROCEDUREPostoperative pain managmentThe intravenous analgesia pump was placed until 48 h after surgery;On the second day after surgery, celecoxib (200 mg bid) was administered orally, and buprenorphine transdermal patch was applied externally until hospital discharge;FNB catheter was placed under the guidance of ultrasound and connected with an analgesic pump, the anesthesia lasted until 48 h after surgery ‡

Timeline

Start date
2016-03-01
Primary completion
2022-03-02
Completion
2023-03-02
First posted
2023-11-09
Last updated
2023-11-09

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06124170. Inclusion in this directory is not an endorsement.