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Comparison of perioperative analgesia in patients undergoing lumbar spine surgery

Comparison of intrathecal morphine vs erector spine plane block for perioperative analgesia in patients undergoing lumbar spine surgery: A prospective single blind randomized controlled trial - NA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057847
Enrollment
74
Registered
2023-09-19
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Health Condition 1: G541- Lumbosacral plexus disorders

Interventions

Intervention1: PONV will be treated with Ondansetron 0.15 mg kg intravenously: 24hrs Control Intervention1: PONV will be treated with Ondansetron 0.15 mg kg intravenously: 24hrs

Sponsors

Department of Neurosurgery
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient of either sex, Age group of20-65years ASA I or II Lumbar spine surgery

Exclusion criteria

Exclusion criteria: Patient Refusal Coagulation disorders Allergies to morphine or study drugs Revision lumbar surgeries Severe respiratory illness (COPD, OSA) Psychiatric illness Pregnancy or Lactation Chronic opioid or analgesic use/abuse

Design outcomes

Primary

MeasureTime frame
oTo compare the analgesia using numeric rating scale (NRS) in intrathecal morphine vs erector spine plane block for perioperative analgesiain patient undergoing lumbar spine surgery.Timepoint: 24 to 48hrs

Secondary

MeasureTime frame
o To compare the sedation score o To compare the patient satisfaction score o To compare the consumption of rescue analgesic o To compare the hemodynamic (HR, SBP, DBP, MAP, RR, SpO2) o To study the complications (PONV, Respiratory depression, Bradycardia, Pruritus) Timepoint: 48hrs

Countries

India

Contacts

Public ContactProf GP Singh

King Georges Medical University Lucknow

gpsinghkgmu@gmail.com9415023076

Outcome results

None listed

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