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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06321952
Other study ID # GTanareesuchoti
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 17, 2021
Est. completion date February 1, 2024

Study information

Verified date March 2024
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A randomized controlled trial was conducted with 72 participants who had moderate knee osteoarthritis (Kellgren and Lawrence grade 2-3). The patients were randomly assigned to either the robotic-assisted or gyroscopic-assisted group. Baseline characteristics, including age, body mass index, length of stay, and estimated blood loss, were recorded. The primary outcome measure was the accuracy of the hip knee angle, measured by scannogram film preoperatively and postoperatively at 3 months. Secondary outcomes included functional outcomes (KOOS, Oxford knee score, EQ-5D-5L, range of motion) assessed preoperatively and postoperatively at 3 months, as well as at 6 months postoperatively.


Description:

Introduction: Primary total knee arthroplasty is considered the gold standard treatment for end-stage osteoarthritis of the knee. The primary objective of this surgical procedure is to restore mechanical alignment. At Siriraj Hospital, we employ technology to enhance the accuracy of our surgical procedures. The purpose of this study is to compare the accuracy of robotic-assisted surgery (ROSA) and gyroscope-based surgery in primary total knee arthroplasty. Methods: A randomized controlled trial was conducted with 72 participants who had moderate knee osteoarthritis (Kellgren and Lawrence grade 2-3). The patients were randomly assigned to either the robotic-assisted or gyroscopic-assisted group. Baseline characteristics, including age, body mass index, length of stay, and estimated blood loss, were recorded. The primary outcome measure was the accuracy of the hip knee angle, measured by scannogram film preoperatively and postoperatively at 3 months. Secondary outcomes included functional outcomes (KOOS, Oxford knee score, EQ-5D-5L, range of motion) assessed preoperatively and postoperatively at 3 months, as well as at 6 months postoperatively.


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date February 1, 2024
Est. primary completion date October 22, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 55 Years and older
Eligibility Inclusion Criteria: - primary osteoarthritis knee with indicated for total knee replacement - age equal or more than 55 years old Exclusion Criteria: - revision surgery - deformity greater than 15ยบ - Intra/Post operative complication

Study Design


Related Conditions & MeSH terms


Intervention

Device:
ROSA robotic assist TKA
total knee replacement with ROSA robotic assist
Procedure:
iassist TKA
total knee replacement with iassist

Locations

Country Name City State
Thailand Siriraj Hospital Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary accuracy of Robotic Assisted Surgery and Gyroscopic Based Instrument accuracy of the hip knee angle, measured by scannogram film preoperatively and postoperatively at 3 months preoperative and postoperative 3months
Secondary Functional Outcome of Robotic Assisted Surgery and Gyroscopic Based Instrument functional outcomes (KOOS score) score 0-100 in each domain of 4 domains 0=worst, 100=good preoperative and postoperative 3months and 6months
Secondary Functional Outcome of Robotic Assisted Surgery and Gyroscopic Based Instrument functional outcomes (Oxford knee score) score 0-48 0=worst, 48=good preoperative and postoperative 3months and 6months
Secondary Functional Outcome of Robotic Assisted Surgery and Gyroscopic Based Instrument functional outcomes (EQ-5D-5L) score 5-25, score5=good, 25=worst preoperative and postoperative 3months and 6months
Secondary Functional Outcome of Robotic Assisted Surgery and Gyroscopic Based Instrument functional outcomes (range of motion) preoperative and postoperative 3months and 6months
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