Preoperative Oral Hydration in the Ambulatory Arthroplasty Population

Description

The purpose of this study is to investigate if the consumption of a complex carbohydrate drink preoperatively, decreases the length of stay and causes for failure to launch in patients undergoing ambulatory total joint arthroplasty.

Conditions

Same-day Discharge, Length of Stay

Talk to us

Study Overview

On this page

Study Details

Study overview

The purpose of this study is to investigate if the consumption of a complex carbohydrate drink preoperatively, decreases the length of stay and causes for failure to launch in patients undergoing ambulatory total joint arthroplasty.

Preoperative Oral Hydration in the Ambulatory Arthroplasty Population :A Single-Blinded Randomized Control Trial

Preoperative Oral Hydration in the Ambulatory Arthroplasty Population

Condition
Same-day Discharge
Intervention / Treatment

-

Contacts and Locations

New York

Hospital for Special Surgery, New York, New York, United States, 10021

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Candidates for ambulatory total knee arthroplasty
  • * Candidates for ambulatory total hip arthroplasty
  • * Candidates for ambulatory revision knee arthroplasty (liner exchange only)
  • * Candidates for ambulatory revision hip arthroplasty (liner exchange only)
  • * Case scheduled before noon (12 pm)
  • * Patient agrees to same-day discharge and has a responsible adult to spend the night on the day of discharge
  • * BMI less than 18.5 or greater than 37.0
  • * Patients with diabetes, chronic kidney disease, clotting disorders, or neurological conditions preventing control of the affected limb.
  • * Pregnant women
  • * Patients scheduled as ambulatory due to insurance mandates
  • * Patients with a history of active ischemia, significant valvular disease, significant arrhythmias, obstructive sleep apnea as per Hospital for Special Surgery guidelines, chronic opioid dependence (chronic daily opioid use for six or more months), and glomerular filtration rate \< 60ml/min.

Ages Eligible for Study

18 Years to 75 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Hospital for Special Surgery, New York,

Jose A Rodriguez, MD, PRINCIPAL_INVESTIGATOR, Hospital for Special Surgery, New York

Study Record Dates

2025-01-24