ESP Block vs. Traditional Pain Management for ERAS

Last updated: March 5, 2020
Sponsor: Soroka University Medical Center
Overall Status: Active - Recruiting

Phase

3

Condition

Acute Pain

Post-surgical Pain

Chronic Pain

Treatment

N/A

Clinical Study ID

NCT04299035
0355-19-SOR
  • Ages > 18
  • All Genders

Study Summary

Patients undergoing thoracotomy, thoracoscopy or other surgical procedures involving the integrity of the chest wall are always in a special point of interest of both surgical and anesthesiological specialities. Most of the patients will describe the pain after thoracic surgery as severe. It might lead to a number of serious complications: respiratory failure due to splinting; inability to clear secretions by effective coughing, with resulting pneumonia; and turning into a chronic pain: the post-thoracotomy pain syndrome.

Traditional pain management in these groups of patients — such as opiate treatment, thoracic epidural analgesia, and non-opioid drugs — may have serious side effects. Large doses of opiates suppress the cough reflex and lead to respiratory depression with subsequent re-intubation and re-ventilation. Thoracic epidural analgesia, though being considered paramount among other analgesic options, requires a significant clinical experience. Still, it might be insufficient for satisfactory pain control and even complicated with pneumothorax, total spinal anaesthesia and inadvertent intravascular injection. Non-steroidal anti-inflammatory drugs (NSAIDs) and Tramadol are weak analgesics inadequate for severe pain control and might be responsible for gastrointestinal bleeding.

We suggest performing erector spinae plane block for intraoperative and postoperative pain management due to the ease of use and better analgesic effect. What remains is hard proof for the clinical efficacy and safety of this block, followed by a demonstration of the uptake of it in the hands of non-regional anaesthetists.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • all consecutive adult patients who undergo thoracic, spinal or abdominal surgery inSoroka Medical Center, and agree to participate in the study, older than 18 years, whomeet criteria of ASA physical status I-II-III-IV class.

Exclusion

Exclusion Criteria:

  • Unconscious or mentally incompetent patients or those who refuse to participate in thestudy.

Study Design

Total Participants: 300
Study Start date:
March 05, 2020
Estimated Completion Date:
September 05, 2021

Connect with a study center

  • SorokaUMC

    Beersheba,
    Israel

    Active - Recruiting

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