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Does Fluid Replacement From Preoperative NPO Status Improve Postoperative Recovery

NCT02638623 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2020-11-20

Study results available
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Summary

The investigators are testing the hypothesis that administering 2L of body temperature warmed lactated ringer's intravenously prior to surgery can optimize the postoperative and recovery of patients undergoing total hip and total knee arthroplasty.

Conditions

Interventions

DRUG

Lactated Ringer

2L Lactated Ringer administered prior to primary knee or hip arthroplasty

DRUG

Placebo

No additional fluids will be administered

Sponsors & Collaborators

  • West Virginia University

    lead OTHER

Principal Investigators

  • Matthew J Dietz, MD · West Virginia University Department of Orthopaedics

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-10-31
Primary Completion
2016-10-31
Completion
2016-12-31

Countries

  • United States

Study Locations

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Entities

Drugs
Diseases

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 NCT02638623 on ClinicalTrials.gov