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Comparison of Erector Spina Block with Ropivacaine and Erector Spina Block with Ropivacaine and Epinephrine on Intraoperative Bleeding and Duration of Analgesia in Posterior Lumbar Spine Fusion Surgery

Comparison of Erector Spina Block with Ropivacaine and Erector Spina Block with Ropivacaine and Epinephrine on Intraoperative Bleeding and Duration of Analgesia in Posterior Lumbar Spine Fusion Surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210415050983N12
Enrollment
64
Registered
2025-06-24
Start date
2025-09-23
Completion date
Unknown
Last updated
2025-07-21

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

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 or systemic infection 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 , 6 , 12 and 24 hours after surgery. Method of measurement: Numeric Rating Scale(NRS).

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