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NCT02186795 Clinical Trial

Total Hip Arthroplasty Outcomes With Regional and Multimodal Analgesia

Arthritis Clinical Trial

— THA  

Official title:
Improvement in Total Hip Arthroplasty Patient Outcomes With Regional Anesthesia and Multimodal Analgesia: A Retrospective Analysis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02186795
Other study ID # THA Retrospective Analysis
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 2013
Est. completion date March 2014

Study information
Verified date June 2018
Source Medical University of South Carolina
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility
Status Completed
Enrollment 117
Est. completion date March 2014
Est. primary completion date March 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Primary total hip arthroplasty, (identified by current procedural terminology (CPT) code 27130) and

2. Either a) Epidural or b) Lumbar plexus peripheral nerve block with the administration of multimodal medication after July 2012.

Exclusion Criteria:Exclusion criteria include THA Revision, ICU admission postoperatively, and dementia, not allowing pain score communication.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Medical University of South Carolina Charleston South Carolina

Sponsors (1)
Lead Sponsor Collaborator
Medical University of South Carolina

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Opiate Consumption Cumulative 48 Hours Opiate Consumption in Intravenous (IV) Morphine mg Equivalents (MME) 48 hours postoperative
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