Pectointercostal Fascial Plane Block Versus Transversus Thoracic Plane Block In Adult Cardiac Surgery Patients
NCT ID: NCT05323305
Last Updated: 2022-04-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
60 participants
INTERVENTIONAL
2022-03-30
2022-12-31
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
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Pectointercostal Group (n=30)
They will receive ultrasound-guided pectointercostal fascial block after induction of anesthesia with equal dose before extubation in the intensive care.
ultrasound guided regional block
Bupivacaine injection by the use of ultrasound in the pectointercostal fascial plane in one group and in the trasversus thoracic plane in the other group.
Transversus thoracic Group (n=30)
They will receive ultrasound-guided ultrasound-guided transversus thoracic plane block after induction of anesthesia with equal dose before extubation in the intensive care.
ultrasound guided regional block
Bupivacaine injection by the use of ultrasound in the pectointercostal fascial plane in one group and in the trasversus thoracic plane in the other group.
Interventions
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ultrasound guided regional block
Bupivacaine injection by the use of ultrasound in the pectointercostal fascial plane in one group and in the trasversus thoracic plane in the other group.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Elective cardiac surgery.
Exclusion Criteria
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
18 Years
ALL
No
Sponsors
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Alexandria University
OTHER
Responsible Party
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Principal Investigators
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islam Omar, MD
Role: STUDY_CHAIR
Lecturer of Anaesthesia and surgical intensive care, Faculty of medicine, Alexandria university
Ibrahim Ibrahim, MD
Role: PRINCIPAL_INVESTIGATOR
Lecturer of Anaesthesia and surgical intensive care, Faculty of medicine, Alexandria university
Moustafa Halwag, MD
Role: STUDY_DIRECTOR
Lecturer of Anaesthesia and surgical intensive care, Faculty of medicine, Alexandria university
Locations
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Alexandria University Hospitals
Alexandria, , Egypt
Countries
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Central Contacts
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Ibrahim Ibrahim, MD
Role: CONTACT
Other Identifiers
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0305468
Identifier Type: -
Identifier Source: org_study_id
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