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Modified Enhanced Recovery After Oblique Lateral Interbody Fusion Surgery — MERAOLIS  

Lumbar Spinal Stenosis Clinical Trial

Official title:
Modified Enhanced Recovery After Oblique Lateral Interbody Fusion Surgery: a Randomised Controlled Trial

Clinical Trial Summary

The goal of this randomized clinical trial is to investigate whether modified enhanced recovery after surgery (ERAS) in oblique lumbar interbody fusion (OLIF) can shorten the postoperative hospital stay among patients with lumbar degenerative disease. The main questions it aims to answer are: Whether ERAS can shorten the postoperative hospital stay. Whether modified ERAS can improve postoperative functional recovery, improve functional score and pain score, reduce hospitalization costs, improve mental state, and improve abdominal indicators, etc. Participants will be randomized into modified ERAS group, or control group.

Clinical Trial Description

The main questions it aims to answer are: Whether ERAS can shorten the postoperative hospital stay. Whether modified ERAS can improve postoperative functional recovery, improve functional score and pain score, reduce hospitalization costs, improve mental state, and improve abdominal indicators, etc. Participants will be randomized into modified ERAS group, or control group. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05854043
Study type Interventional
Source Xuanwu Hospital, Beijing
Contact Lei Zhang, MD
Phone 17610549095
Email zhanglei@xwhosp.org
Status Recruiting
Phase N/A
Start date April 1, 2023
Completion date April 1, 2025
View Details
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