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Traditional vs Oral Fluid Management in Total Knee Arthroplasty

NCT03719378 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2021-03-16

Study results available
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Summary

Purpose: Evidence-based guidelines on optimal perioperative fluid management have not been established in patients undergoing orthopaedic surgery. Recent randomized trials in major abdominal surgery suggest that large amounts of IV fluid may increase morbidity and hospital stay. This study will investigate the effects of two regimens of intraoperative fluid management ("traditional" vs. "oral") with physiologic and patient function as primary outcome measures after surgery.

Conditions

  • Arthroplasty, Replacement, Knee

Interventions

OTHER

Pre Operative Oral Fluids

Patients will be self hydrating prior to their total knee replacement.

Sponsors & Collaborators

  • Colorado Joint Replacement

    lead OTHER

Principal Investigators

  • Jason Jennings, MD · Colorado Joint Replacement

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-10-13
Primary Completion
2018-09-10
Completion
2018-09-10

Countries

  • United States

Study Locations

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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 NCT03719378 on ClinicalTrials.gov