Status:
TERMINATED
Serratus Anterior or Erector Spinae Block for Hybrid Arrhythmia Ablation Surgery
Lead Sponsor:
Universitair Ziekenhuis Brussel
Conditions:
Arrhythmia
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
The purpose of this study is to evaluate differences between single-shot EQUAL ropivacaine doses of the serratus anterior plane block (SAPB) or erector spinae plane block (ESPB) injection, when used a...
Detailed Description
This clinical investigation is an interventional uni-center, prospective, open, randomized, double arm, blinded to the pain physician and the patient, clinical evaluation. To ensure the same number o...
Eligibility Criteria
Inclusion
- Age 18-80 years.
- Provision of signed informed consent prior to any study-specific procedure
- Selected for Hybrid Rhythm ablation surgery (ISNT, VT, AF)
- American Society of Anesthesiologist physical Status I to III
- Dutch, French or English speaking
- Ability to follow the study protocol
- BMI \> 35 kg/m2 . BMI or Body mass index will be obtained from body weight in kg divided by the square of the length in meter and is expressed in kg/m2
- \-
Exclusion
- a. History of chronic pain or drug treatment abuse
- b. Depression, psychiatric morbidity or mal-adaptive coping behaviour
- c. Neuropathy
- d. Severe anxiety or other mental ailment, taking drugs affecting their capacity to assess pain (gabapentin, pregabalin, opiod use)
- e. Chronic or acute skin infection of the back or the lateral thorax
- f. Hypersensitivity to ropivacaine
- g. Severe hepatic, renal , pulmonary or cardiac (EF \< 30%) disease or refuse to participate to the study..
Key Trial Info
Start Date :
October 2 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2024
Estimated Enrollment :
28 Patients enrolled
Trial Details
Trial ID
NCT04868058
Start Date
October 2 2020
End Date
December 1 2024
Last Update
December 18 2025
Active Locations (1)
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1
Universitair Ziekenhuis
Brussels, Brussels Capital, Belgium, 1090