Does Fluid Replacement From Preoperative NPO Status Improve Postoperative Recovery
Completed · Not applicable · Has a placebo group
Conditions studied: Osteoarthritis
In brief
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.
Key facts
- Study ID
- NCT02638623
- Run by
- West Virginia University
- People needed
- 52
- Starts
- 2015-10-01
- Expected to finish
- 2016-12-01
- Last updated by the study team
- 2020-11-20
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- All patients >= 18 years of age, undergoing a total primary knee or hip arthroplasty
You may not qualify if…
- Patients weighing less than 80 kg.
- Patients undergoing irrigation and debridement, explantation, or revision will not be eligible.
- history of kidney disease, congestive heart failure, pulmonary edema, cirrhosis of the liver, or history of systemic fluid overloard will be excluded from the study.
- No one will be excluded based on gender, ethnicity or race.
Where it is running
- WVU Medicine Department of Orthopaedics — Morgantown, West Virginia, United States
Full record on ClinicalTrials.gov
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