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NCT05998538 Clinical Trial

Patients With Higher BMI Produces More Postoperative Drainage Volume and Length of Stay in Cross-Sectional Study

Osteoarthritis, Knee Clinical Trial

Official title:
Patients With Higher BMI Produces More Postoperative Drainage Volume and Longer Length of Stay in Cross-Sectional Study: a Comparison of Total vs Partial Knee Arthroplasty

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05998538
Other study ID # 23082020
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 23, 2019
Est. completion date December 7, 2022

Study information
Verified date August 2023
Source Indonesia University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Partial knee arthroplasty theoretically produces less blood loss compared to total knee arthroplasty (TKA) due to a lesser invasive procedure. Medial unicompartmental knee arthroplasty (UKA) is the most common partial knee arthroplasty performed due used due to the most commonly impacted medial knee. This study compared the postoperative drainage volume and length of stay (LOS) of TKA vs UKA and evaluated its comparison with patient characteristics.

Description:

Theoretically, UKA will produce less blood loss due to a shorter skin incision, quadriceps sparing muscle approach, persistence of cruciate ligaments, and less femorotibial dislocation.7 However, studies investigating drainage volume in UKA are still limited. In this study, we compared the drainage volume of patients undergoing TKA vs UKA and evaluated several parameters that contributed the production. This study has not received any funding or grant.

Recruitment information / eligibility
Status Completed
Enrollment 120
Est. completion date December 7, 2022
Est. primary completion date October 21, 2022
Accepts healthy volunteers No
Gender All
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria: - grade 4 Osteoarthritis Exclusion Criteria: - previous trauma - infection - blood coagulation disorder

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Knee Replacement
Total vs Partial Knee Replacement

Locations
Country Name City State
Indonesia Pondok Indah Hospital Jakarta

Sponsors (1)
Lead Sponsor Collaborator
Indonesia University

Country where clinical trial is conducted

Indonesia, 

Outcome
Type Measure Description Time frame Safety issue
Primary Drainage Volume total drainage volume 3-5 days post op
Secondary LOS length of stay pre-op until drainage removed, 3-6 days post op
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