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Enhanced recovery in lumbar spine surgeries

Enhanced recovery in elective lumbar spine surgeries- A randomized controlled study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068960
Enrollment
150
Registered
2024-06-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: ERAS protocol: Abstinence from alcohol and smoking 4 weeks prior to surgery, proton pump inhibitors pre-op, fasting 6 hours for light non fatty meal and 2 hours for clear liquids, thora

Sponsors

SIMS Hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grades 1 and 2, patients admitted for lumbar spine surgeries including transforaminal interlumbar body fusion, posterior lumbar decompression and stabilization, lumbar microdissectomy and percutaneous lumbar stabilization

Exclusion criteria

Exclusion criteria: ASA grades 3 and 4, patients with major comorbid conditions, pregnant and lactating mothers, obese individuals with BMI more than or equal to 30, patients with drug allergies or egg allergy , patients participating in any other clinical studies, patients with major neurological deficits

Design outcomes

Primary

MeasureTime frame
Postoperative length of stay and total hospitalisation costTimepoint: From time of admission to discharge

Secondary

MeasureTime frame
Readmission rates, postoperative complications, postoperative pain scores, peri operative opioid consumption, length of ICU stay, duration of drainage tube, time to first oral intake , postoperative functional recovery statusTimepoint: 30 days from discharge

Countries

India

Contacts

Public ContactDr Magimairaj

SIMS Hospital

mdavidjayapal@gmail.com9840757749

Outcome results

None listed

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