Comparative analgesic study of supra-inquinal fascia iliaca compartment block and continuous lumbar epidural for total hip replacement; A retrospective study

Recruiting

• Conditions: umeric rating score (NRS) at rest and movement from 0 (no pain) to 10 (worst imaginable pain) at 24 hours postoperative in patients who were undergone total hip replacement; Supra-inquinal fascia iliaca compartment block; Continuous lumbar epidural analgesia; Total hip replacement; Retrospective study

• Registration Number: TCTR20210825003
• Lead Sponsor: Faculty of Medicine Ramathibodi Hospital, Mahidol University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-08-25
• Study Completion: 2021-09-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 58

Inclusion Criteria

Patients who were undergone total hip replacement using supra-inquinal fascia iliaca compartment block and continuous lumbar epidural technique from January 2018 to December 2020

Exclusion Criteria

Completeness (percent of data fields having values entered) of less than 50%.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain intensity 24 hours postoperatively Numeric rating score (NRS) at rest and movement from 0 (no pain) to 10 (worst imaginable pain) at 24 hours postoperative

Secondary Outcome Measures

Name	Time	Method
Cumulative morphine consumption 48 hours postoperatively Report from the device used,Hypotension Only 1 time Incidence (%),Weakness Only 1 time Incidence (%),Nausea/vomit Only 1 time Incidence (%),Length of hospital stay Only 1 time Duration from the report (days),Patient satisfaction on overall postoperative pain management Only 1 time Likert scale (0-10)