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ENROLLING BY INVITATION
NCT06580899
PHASE4

Intra-Articular Catheter Total Knee Arthroplasty

Sponsor: OrthoCarolina Research Institute, Inc.

View on ClinicalTrials.gov

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

DEVICE

Intra-articular catheter

Intra-articular catheter pump with existing standard-of-care multimodal pain management protocol in the immediate post-op period

OTHER

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