Medical University of South Carolina
Charleston, South Carolina, 29425, United States
NCT Number: NCT02186795
The goal of this retrospective chart review is to evaluate if the implementation of lumbar plexus block placement for postoperative pain and administration of multimodal oral analgesia have improved conditions in the postoperative period for patients undergoing total hip arthroplasty when compared to the placement of epidurals for postoperative pain management.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Charleston, South Carolina, 29425, United States
Primary outcome: 48 hour opiate consumption in patients following THA. ' Secondary outcome: Time to first ambulation, assitstance needed with ambulation, opiate and regional related side effects, time to discharge orders.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
-
Exclusion criteria
Exclusion criteria include THA Revision, ICU admission postoperatively, and dementia, not allowing pain score communication.
-
Time frame: 48 hours postoperative
Cumulative 48 Hours Opiate Consumption in Intravenous (IV) Morphine mg Equivalents (MME)
Medical University of South Carolina
Other
Improvement in Total Hip Arthroplasty Patient Outcomes With Regional Anesthesia and Multimodal Analgesia: A Retrospective Analysis
Acronym: THA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT00762944
Arthritis, Arthroplasty
Indianapolis, Indiana, United States
View Trial DetailsNCT04849884
Arthroplasty, Knee
New York, United States
View Trial DetailsNCT07574775
Arthritis, Arthroplasty
Paris, France
View Trial DetailsNCT05449327
Arthroplasty, Cardiovascular Diseases
Chiayi City, Taiwan
View Trial Details