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Parasternal Block Combined With Rectus Sheath Block for Cardiac Surgery Under Sternotomy

NCT05764616 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 58

Last updated 2023-11-27

No results posted yet for this study

Summary

The aim of this randomized controlled trial is to examine the effect of ultrasound guided bilateral Parasternal Nerve Block combined with rectus sheath block on preoperative analgesia, opioid consumption and respiratory function in patients undergoing cardiac surgery via sternotomy. Half of participants will receive General Anesthesia combined with bilateral parasternal block and rectus sheath block while the other half receive General Anesthesia combined with bilateral parasternal block and infiltration of drainage exits sites with local anesthetic (without performing rectus sheath block)

Conditions

  • Cardiac Disease
  • Surgery
  • Analgesia
  • Acute Pain
  • Postoperative Pain

Interventions

PROCEDURE

PARASTERNAL BLOCK

After induction of general anesthesia, an ultrasound-guided Parasternal Block will be performed with 20 mL of ropivacaine 0.5 % per side.

PROCEDURE

LOCAL INFILTRATION OF DRAINAGE EXIT SITES

At the end of surgery, a local infiltration of drainage exit sites will be performed with 10 mL of ropivacaine 0.25% per side

PROCEDURE

RECTUS SHEATH BLOCK

At the end of surgery, a rectus sheath block will be performed with 10 mL of ropivacaine 0.25% per side.

Sponsors & Collaborators

  • Campus Bio-Medico University

    lead OTHER

Principal Investigators

  • Giuseppe Pascarella, MD · University Hospital Campus Biomedico of Rome

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-21
Primary Completion
2023-10-10
Completion
2023-11-10

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05764616 on ClinicalTrials.gov