UnknownNot Applicable

Does ESP Block Reduce Pain and Opiates Consumption After Surgery

Israel300 participantsStarted 2020-09-01

Plain-language summary

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

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. All patients undergoing thoracic surgery, older ≥18 years
✓. Patients who meet criteria of ASA (american society of anesthesiologists) physical status I-II-III class.

Exclusion criteria

✕. Patients who will be unconscious or mentally incompetent
✕. Patients refusal to participate in the study
✕. ASA -IV -V
✕. Patient with coagulopathy
✕. Hemodynamically unstable (systolic blood pressure \< 90, heart rate (HR) \> 100)
✕. Allergy to local anesthetic drugs or opioids
✕. Pregnant patient
✕. History of opioid abuse

What they're measuring

VAS score

Timeframe: postoperative - 1 hour

VAS score

Timeframe: postoperative - 4 hour

VAS score

Timeframe: postoperative - 8 hour

VAS score

Timeframe: postoperative - 12 hour

VAS score

Timeframe: postoperative - 24 hour

VAS score

Timeframe: postoperative - 48 hour

VAS score

Timeframe: postoperative - 72 hour

VAS score

Timeframe: day 7 postoperative

VAS score

Timeframe: day 14 postoperative

Trial details

NCT IDNCT05512897

SponsorMichael Dubilet MD

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-09

Contact for this trial

michael dubilet, md

972-54-6260728 mikl.dubilet@gmail.com

View on ClinicalTrials.gov More Post Operative Pain trials