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Clinical Trials/NCT06710457
NCT06710457CompletedNot Applicable

Effect of Erector Spinae Plane Block on Postoperative Nausea and Vomiting in Lumbar Disc Herniation Surgery

Ankara City Hospital Bilkent1 site in 1 country81 target enrollmentStarted: December 11, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
81
Locations
1
Primary Endpoint
PONV

Study Overview

Brief Summary

This study will investigate the hypothesis that preoperative erector spinae plane (ESP) block will reduce the incidence of postoperative nausea and vomiting (PONV) in patients undergoing elective lumbar disc herniation (LDH) surgery. PONV was defined as the presence of nausea and vomiting within 24 hours postoperatively.

Detailed Description

The study will include patients aged 18 years and older, with (American Society of Anesthesiologists) ASA physical status I and II, and scheduled for single-level lumbar disc herniation surgery under general anesthesia. Patient characteristics (age, gender, body mass index, etc.), Apfel score, postoperative nausea and vomiting (PONV) status, intraoperative opioid use requirement, surgical duration, postoperative pain status, rescue analgesic and emetic requirement will be recorded. The primary outcome parameter will be the PONV incidence within the postoperative 24 hours. PONV severity during this period will be assessed using a Likert scale from 0 to 10. PONV will be defined as vomiting, marked nausea (numerical rating scale [NRS] ≥4), and/or need for rescue medication. Patients will be assessed for PONV at 0, 2, 4, 12, and 24 hours using the Likert scale. Nausea and its severity, vomiting attacks, need for intraoperative opioid use, pain and its severity, need for additional analgesics, and administration of antiemetic rescue medication will be evaluated as secondary outcome parameters.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age 18 and above
  • •ASA physical status I to II
  • •One lumbar disc herniation surgery under general anesthesia

Exclusion Criteria

  • •body mass index >35 kg/m²)
  • •history of drug use
  • •nausea and vomiting before surgery
  • •psychiatric disorders
  • •use of antipsychotic or antiemetic drugs
  • •severe heart disease
  • •central nervous system diseases
  • •vertebrobasilar artery insufficiency
  • •cytostatic therapy
  • •vestibular diseases
  • •renal and/or hepatic dysfunction
  • •pregnant patients
  • •presence of bleeding diathesis
  • •patients in a condition where cooperation cannot be established in the post-operative period (mental retardation etc.)
  • •patient's refusal to accept the block procedure
  • •allergy to local anesthetics
  • •injection site infection

Arms & Interventions

Erector spinae plane (ESP) block

Active Comparator

Patients will receive an erector spinae plane (ESP) block in addition to standard medical treatment to prevent PONV and postoperative pain.

Intervention: ESP (Other)

No Erector spinae plane (ESP) block

Active Comparator

Patients will receive standard medical treatment to prevent PONV and postoperative pain.

Intervention: No ESP (Other)

Outcomes

Primary Outcomes

PONV

Time Frame: 24 hours

The primary outcome of the study was the incidence of postoperative nausea and/or vomiting

Secondary Outcomes

  • Severity of nausea(24 hours)
  • 11 - point numerical rating scale (NRS)(24 hours)
  • Rescue antiemetic requirement(24 hours)
  • Rescue analgesic requirement(24 hours)
  • intraoperative opioid requirement(intraoperative time)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Gökhan Erdem

Anesthesiology and Reanimation specialist doctor

Ankara City Hospital Bilkent

Study Sites (1)

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