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Bilateral Bi-level Erector Spine Plane Block as a Component of General Anesthesia in Surgical Correction of Spinal Deformations

Unknown statusNot applicableNCT04697498
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Improving the anesthesiology management for surgical correction of spinal deformations with introducing the diagnostic methods and treatment strategy of acute pain, preventing the evolution of chronic pain. Development and implementation in clinical practice perioperative intensive care protocols for surgical correction of spinal deformities.

Study details

Official title
Bilateral Bi-level Erector Spine Plane Block as a Component of General Anesthesia in Surgical Correction of Spinal Deformations
Conditions
  • Scoliosis
  • Spinal Deformity
  • Acute Pain
  • Chronic Pain
  • Postoperative Pain
  • Anesthesia
  • Regional Anesthesia Morbidity
  • Anesthesia, Local
  • Anesthesia Complication
  • Hyperalgesia
  • Intraoperative Complications
  • Intraoperative Hypotension
  • Intraoperative Blood Loss
  • Intraoperative Bleeding
  • Intraoperative Neurological Injury
  • Intraoperative Injury
  • Coagulation Disorder
  • Postoperative Nausea and Vomiting
  • Postoperative Cognitive Dysfunction
  • Neuropathic Pain
  • Nutrient Deficiency
  • Nutrition Disorders
  • Ventilator-Induced Lung Injury
Interventions
  • Procedure: Bilateral bi-level Erector spine plane block
  • Procedure: General anaesthesia
Sponsor
Lviv National Medical University
Start date
2020-12-16
Primary completion
2025-12
Sex
All
Age range
from 12 Years to 90 Years
Results posted
No results posted in this snapshot
Countries
Ukraine
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Informed consent of the patient or his legal representatives to participate the study. 2. Spinal deformity that requires surgical correction. 3. No known allergies to local anaesthetics. 4. Negative intradermal test for sensitivity to local anaesthetics. Exclusion Criteria: 1. Refusal of the patient or his legal representatives to participate the study 2. Diabetes mellitus, known allergy to local anaesthetics 3. Acute spinal cord injury 4. Physical status according to classification ASA III and more 5. A positive intradermal test for sensitivity to a local anaesthetic.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04697498