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Comparing the effects of bupivacaine and bupivacaine-methylprednisolone in ultrasound guided erector spinae plane block on postoerative pain in Lumbar spine surgery

Comparing the effects of bupivacaine and bupivacaine-methylprednisolone in ultrasound guided erector spinae plane block on postoerative pain in Lumbar spine surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210415050983N6
Enrollment
64
Registered
2024-04-18
Start date
2024-05-21
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Lumbar discopathy. Other intervertebral disc degeneration, lumbar region

Interventions

Intervention 1: Control group: After anesthesia and change of position to peron before surgery, in sterile conditions, using peripheral nerve block needle (stimuQuik, ARROW use) with sonosite-Nerve U

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients 18-65 years old are candidates for two or three level spine surgery ASA score 1-2 Normal kidney and liver function Patient consent to perform the block No history of allergies to local anesthetics No drug addiction No diabetes

Exclusion criteria

Exclusion criteria: Increase the scope of surgery to more than three level Extending the length of surgery for more than 6 hours Block site infection or systemic History of anticoagulant use

Design outcomes

Primary

MeasureTime frame
Intraoperative isoflurane Consumption in tow groups. Timepoint: Before the start of anesthesia and after the end of anesthesia. Method of measurement: By a graduated glass based on mL.;Intraoperative fentanyl consumption in the two groups. Timepoint: End of surgery. Method of measurement: Dosage consumed based on mcg.;Pain after surgery. Timepoint: 0, 1 and 6 hours after surgery and one month after surgery. Method of measurement: NRS.;Blood sugar. Timepoint: After surgery up to 24 months. Method of measurement: Blood test.

Secondary

MeasureTime frame
Nausea and vomiting. Timepoint: 0, 1 and 6 hours after surgery. Method of measurement: Ask the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSogol Asgari

Shahid Beheshti University of Medical Sciences

Drasgari98429@gmail.com+98 21 5541 9005

Outcome results

None listed

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