MedTrace Logo

IPACK and Adductor Canal Catheter Patient Outcomes for TKAs?

NCT03774966 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2020-02-19

No results posted yet for this study

Summary

This study evaluates the addition of the IPACK block to the adductor canal block and catheter in the pain management of total knee arthroplasty. Half of participants will receive the adductor canal block and catheter with the IPACK block, while the other half will receive the adductor canal block and catheter only.

Conditions

  • Surgery
  • Acute Pain

Interventions

PROCEDURE

Adductor Canal Block + Catheter & IPACK block

Adductor Canal Block + Catheter \& IPACK block

PROCEDURE

Adductor canal block + catheter

Adductor canal block + catheter

Sponsors & Collaborators

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-02-12
Primary Completion
2019-05-28
Completion
2019-05-28
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03774966 on ClinicalTrials.gov