At a glance
ClinicalIndex Comparison RecordN/ACompleted· 52 enrolled
Drug / intervention
Lactated Ringer +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Does Fluid Replacement From Preoperative NPO Status Improve Postoperative Recovery and Reduce Complications in Arthroplasty Patients?
In Brief
A clinical study evaluating Lactated Ringer and Placebo for Osteoarthritis. Completed, enrolled 52 participants across 1 site.
Detailed 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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsOsteoarthritis
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartOct 2015
First PostedDec 2015
Primary CompletionOct 2016
Study CompletionDec 2016
TodayJul 2026
First PostedDec 23, 2015
Enrollment StartOct 1, 2015
Primary CompletionOct 1, 2016
Study CompletionDec 1, 2016
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 10.5 years ago
Interventions
Lactated Ringerdrug
2L Lactated Ringer administered prior to primary knee or hip arthroplasty
Placebodrug
No additional fluids will be administered