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A clinical Trial to Assess the Efficacy of Enhanced Recovery After Surgery (ERAS) protocol in recovery of patients undergoing Elective Lumbar Spinal fusion

A Randomised Controlled Trial to Assess the Efficacy of Enhanced Recovery After Surgery (ERAS) protocol in Elective Lumbar Spinal fusion - ERAS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084026
Enrollment
70
Registered
2025-04-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified

Interventions

Intervention1: Enhanced Recovery After Surgery ERAS protocol in Elective Lumbar Spinal fusion: Patients undergoing elective lumbar spinal fusion will receive perioperative care based on the Enhanced R

Sponsors

Dr M Siva Prasad
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Age greater than 18 years 2) Undergoing elective lumbar spinal fusion

Exclusion criteria

Exclusion criteria: 1)Patients not consenting for the study. 2)Patients undergoing urgent or emergent surgery. 3)Vulnerable patients such as pregnant women. 4)Infective spine pathology, tumours.

Design outcomes

Primary

MeasureTime frame
Length of hospital stayTimepoint: 2 years—

Secondary

MeasureTime frame
Assessment of pain control in the hospital using Visual Analogue Scale (VAS) pain scores before surgery, at discharge, and average daily scores.Timepoint: 2 years;Total postoperative analgesic consumption during hospitalization and patient-reported analgesic usage one month post-surgery.Timepoint: 2 years;Postoperative mobilization and ambulation in the hospital, including time to ambulation and incidence of hospital falls. Mobilization refers to extremity movement and ambulation denotes walking with or without assistance.Timepoint: 2 years;Utilization and duration of Foley catheterization, as well as the need for postoperative straight catheterization.Timepoint: 2 years;Assessment of inflammatory markers.Timepoint: 2 years—

Countries

India

Contacts

Public ContactMUMMAKA SIVA PRASAD

SVIMS , TIRUPATI, INDIA

sivamsp143@gmail.com08317609601

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026