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Efficacy of Erector Spinae Plane Block Analgesia After Off Pump Cardiac Surgery

Efficacy of Erector Spinae Plane Block on Postoperative Analgesia and Recovery After Off Pump Cardiac Surgery: A Randomised Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05769309
Acronym
ESPB
Enrollment
50
Registered
2023-03-15
Start date
2023-03-22
Completion date
2023-12-25
Last updated
2024-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Brief summary

In this study the investigators will investigate the efficacy of ESPB as a part of Enhanced recovery after surgery on postoperative analgesia and recovery criteria after off pump cardiac surgery.

Detailed description

General anaesthesia will be induced by 0.05 mg/kg midazolam, 3 µg/kg fentanyl, 1-2mg/kg propofol, and 0.5mg/kg of Atracurium. After induction, bilateral erector spinae plane block will be performed in the block group. Intraoperative analgesia will be achieved by fentanyl boluses of 0.5-to-1 µg/kg titrated according to haemodynamic parameters. Postoperative analgesia will be managed by paracetamol 1000 mg /6hours and morphine 1-2mg boluses when pain score ≥4 1 to 2 mg to be repeated every 5 minutes if needed.

Interventions

PROCEDUREErector spinae block

After induction, the patients will be administered bilateral Erector spinae block with 20 ml of 0.25 % bupivacaine

DRUGFentanyl

fentanyl boluses of 0.5-to-1 µg/kg titrated according to haemodynamic parameters.

Sponsors

Menoufia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* age 18-70 years * ejection fraction of \> 45% * undergoing elective off-pump cardiopulmonary bypass surgery

Exclusion criteria

* vertebral anomalies * intra-aortic balloon pump in the preoperative period * acute myocardial infarction * local infection at the site of block * allergy to the local anesthetic used * morbid obesity, psychiatric disorders, neurologic deficits, alcohol and chronic opioid abuse, and patients with bleeding diathesis.

Design outcomes

Primary

MeasureTime frameDescription
Total intraoperative and postoperative opioid consumption48 hoursMicrogram and mg

Secondary

MeasureTime frameDescription
mean arterial blood pressure48 hoursmmHg
pain intensity at rest and movement48 hoursnumerical rating score from zero to ten ( 0=no pain, 10 =severe pain )
time to first rescue analgesia24housminutes
Duration of mechanical ventilation24 hourshours
The heart rate48 hoursBeats per minutes
time to ambulation24hourshours
time to oral intake48 hourshours
time of chest drain removal5 dayshours
time of intensive care unit stayone weekhours
time to extubation24hoursmin

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026