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Comparison of Perioperative Outcomes Between Enhanced Recovery After Surgery (ERAS) Protocol and Standard Care in Patients Undergoing Lumbar Spinal Fusion Surgery

Comparison of Perioperative Outcomes Between Enhanced Recovery After Surgery (ERAS) Protocol and Standard Care in Patients Undergoing Lumbar Spinal Fusion Surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250730003
Enrollment
36
Registered
2025-07-30
Start date
2025-07-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Degenerative lumbar spine disease requiring spinal fusion surgery, including conditions such as lumbar spinal stenosis, degenerative disc disease, spondylolisthesis, and other causes of chronic lumbar instability or deformity. Spinal fusion surgery ERAS ERAS protocol Enhanced recovery after surgery Standard care Perioperative outcomes

Interventions

The multidisciplinary ERAS protocol aims to enhance postoperative recovery, reduce complications, shorten hospital stay, and improve overall patient outcomes. The ERAS protocol includes: 1. Preoperati
Experimental Procedure/Surgery,Experimental Procedure/Surgery
Enhanced recovery after surgery (ERAS) protocol ,Standard care

Sponsors

Institute of Orthopaedics, Lerdsin Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective lumbar spinal fusion 2. Aged 18-65 years 3. ASA classification 1-3

Exclusion criteria

Exclusion criteria: 1. Previous history of spinal infection 2. Previous history of spinal fracture 3. Patients with spinal tumors or congenital spinal abnormalities 4. Patients with chronic kidney disease 3-5 5. Having communication problems and difficulty answering research questions 6. Allergy to drug in protocol

Design outcomes

Primary

MeasureTime frame
Length of stay Postoperative Day 0 to Discharge Measured in days from the day of surgery to the day of discharge.

Secondary

MeasureTime frame
Operation time Intraoperative Measured in minutes from skin incision to closure (recorded by surgical team),Intraoperative blood loss Intraoperative Measured in milliliters (mL), based on surgical suction canister volume and gauze weight.,Visual Analog Scale (VAS) Postoperative day 1, day 2, day 3 A 10-cm horizontal line where patients indicate their current level of pain, ranging from 0 (no pain) to 10 (worst imaginable pain),Postoperative opioid consumption Postoperative Day 0 to Discharge Total opioid use converted to morphine equivalent dose (mg), calculated from medication administration records.,Time to mobilization Postoperative Day 0 to Discharge Measured in hours from the end of surgery to the first successful mobilization (sitting, standing, or walking), documented by nursing or physiotherapy staff.,Complication Postoperative Day 0 to Postoperative 3 months Documented clinical complications (e.g., infection, ileus, urinary retention, DVT) recorded from the patient chart and daily progress notes.,30-day readmission Follow-Up at 30 Days Postoperative Percentage of patients readmitted within 30 days post-discharge, verified via hospital records or patient follow-up.,Oswestry Disability Index (ODI) Postoperative 3 months A validated questionnaire assessing disability related to lumbar spine pathology

Countries

Thailand

Contacts

Public ContactNatthason Phusawat

Institute of Orthopaedics, Lerdsin Hospital

natthason.p1996@gmail.com023539844

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026