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Does ESP Block Reduce Pain and Opiates Consumption After Surgery

Unknown statusNot applicableNCT05512897
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)

The patients will be randomly assigned to standard therapy or standard therapy+ESP nerve block. After surgery pain level and narcotic consumption will be measured, and vital signs and side effects will bo monitored for up to 72 hours. 6 months after surgery a phone interview will be conducted to asses chronic pain

Study details

Official title
Compared Erector Spinae Plane Block (ESP) Block for Pain Control With Traditional Pain Management Techniques in Patient Undergoing Thoracic and Abdominal Surgery
Conditions
Interventions
  • Procedure: erector spinea plane block
Sponsor
Michael Dubilet MD
Organization
Soroka University Medical Center
Start date
2020-09-01
Primary completion
2023-09
Sex
All
Age range
from 18 Years
Healthy volunteers
true
Results posted
No results posted in this snapshot
Countries
Israel
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. All patients undergoing thoracic surgery, older ≥18 years 2. Patients who meet criteria of ASA (american society of anesthesiologists) physical status I-II-III class. Exclusion Criteria: 1. Patients who will be unconscious or mentally incompetent 2. Patients refusal to participate in the study 3. ASA -IV -V 4. Patient with coagulopathy 5. Hemodynamically unstable (systolic blood pressure \< 90, heart rate (HR) \> 100) 6. Allergy to local anesthetic drugs or opioids 7. Pregnant patient 8. History of opioid abuse

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05512897