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Pectointercostal Fascial Plane Block Versus Transversus Thoracic Plane Block In Adult Cardiac Surgery Patients

A

Alexandria University

Status

Enrolling

Conditions

Pain, Post Operative

Treatments

Procedure: ultrasound guided regional block

Study type

Interventional

Funder types

Other

Identifiers

NCT05323305
0305468

Details and patient eligibility

About

The study will be designed to compare the analgesic effect of ultrasound-guided pectointercostal fascial plane block versus tansversus thoracic plane block in adult cardiac surgery.

Full description

A prospective study will be carried out in Alexandria Main University Hospitals on 60 adult patients planned for elective cardiac surgery, after approval of the Ethical Committee of Faculty of Medicine, Alexandria, and having an informed written consent taken from patients included in the study. Patients will be categorized into two equal groups; group P (n=30)) will receive ultrasound-guided pectointercostal fascial plane block and group T (n=30) will receive ultrasound-guided transversus thoracic plane block.

All patients will receive the ultrasound-guided block after induction of anesthesia and an equal booster dose of the same block before extubation in the ICU. Patients in both groups will also receive an ultrasound-guided bilateral serratus anterior plane block before extubation.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Adult patient.
  2. Elective cardiac surgery.

Exclusion criteria

  1. Refusal to participate.
  2. Redo or urgent cardiac surgery.
  3. Local infection of the skin at the site of needle puncture.
  4. Allergy to bupivacaine.
  5. Coagulation disorders.
  6. Clinically significant liver or kidney disease, heart failure, moderate to severe pulmonary hypertension.
  7. when extubation is intentionally planned to be delayed

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

60 participants in 2 patient groups

Pectointercostal Group (n=30)
Active Comparator group
Description:
They will receive ultrasound-guided pectointercostal fascial block after induction of anesthesia with equal dose before extubation in the intensive care.
Treatment:
Procedure: ultrasound guided regional block
Transversus thoracic Group (n=30)
Active Comparator group
Description:
They will receive ultrasound-guided ultrasound-guided transversus thoracic plane block after induction of anesthesia with equal dose before extubation in the intensive care.
Treatment:
Procedure: ultrasound guided regional block

Trial contacts and locations

1

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Central trial contact

Islam Omar, MD; Ibrahim Ibrahim, MD

Data sourced from clinicaltrials.gov

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