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Intra-Articular Catheter Total Knee Arthroplasty
Sponsor: OrthoCarolina Research Institute, Inc.
Summary
This is a prospective, randomized clinical trial evaluating three groups. The groups are: Group 1 (Control): Subjects that receive only the existing standard-of-care multimodal pain management protocol and do not receive post-operative intra-articular catheter. Group 2 (Investigational Treatment/Intervention): Subjects that receive the brand 1 intra-articular catheter pump with existing standard-of-care multimodal pain management protocol in the immediate post-operative period. Group 3 (Investigational Treatment/Intervention): Subjects that receive the newer brand 2 intra-articular catheter pump with existing standard-of-care multimodal pain management protocol in the immediate post-operative period.
Official title: Effectiveness of Continuous Local Infiltration Analgesia Intra-Articular Catheters for Pain Relief in Total Knee Replacement
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
65
Start Date
2025-03-14
Completion Date
2026-12-31
Last Updated
2026-04-06
Healthy Volunteers
No
Interventions
Intra-articular catheter
Intra-articular catheter pump with existing standard-of-care multimodal pain management protocol in the immediate post-op period
Routine Standard of Care Treatment
No changes to what would occur outside of the study.
Locations (1)
OrthoCarolina Research Institute, Inc.
Charlotte, North Carolina, United States