Serratus Intercostal Block Versus Epidural Analgesia in Eventration: Prospective Observational Study
NCT ID: NCT06014749
Last Updated: 2025-03-14
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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COMPLETED
80 participants
OBSERVATIONAL
2022-09-01
2025-03-01
Brief Summary
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We conducted an observational study with a low level of intervention. Epidural analgesia prior to general anesthesia and serratus-intercostal block prior to general anesthesia) following the criteria applied in each case according to the operating room anesthesiologist until reaching the sample size and fulfilling the criteria of: abdominal eventration repair, over 18 years of age, ASA I-III. Signature of the IC.
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Detailed Description
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The investigators conducted an observational study with a low level of intervention. Epidural analgesia prior to general anesthesia and serratus-intercostal block prior to general anesthesia) following the criteria applied in each case according to the operating room anesthesiologist until reaching the sample size and fulfilling the criteria of: abdominal eventration repair, over 18 years of age, ASA I-III. Signature of the IC.
We will assess the analgesia provided by both techniques and to compare the results.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Patient under serratus intercostal plane block
patients who will undergo a modified bilateral ultrasound-guided BRILMA block (SIPB) using a high-frequency linear probe (6-15 Hz) and 80 mm needle.
undergo
regional anesthesia
ultrasound
ultrasound guided
Local anesthetic
local anesthetic
patient under epidural analgesia
patients who undergo Epidural Analgesia prior to General Anesthesia and fentanyl 1 mcg/kg approx according to characteristics and needs and upon arrival at the URPA is connected to the PC Levobupi 0.125% at 6 ml / h + rescue boluses of Levobupi 0.125% 4 ml if needed in the 1st hours.
undergo
regional anesthesia
ultrasound
ultrasound guided
Local anesthetic
local anesthetic
Interventions
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undergo
regional anesthesia
ultrasound
ultrasound guided
Local anesthetic
local anesthetic
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* over 18 years old,
* ASA I-III.
* Signature of the IC.
Exclusion Criteria
18 Years
85 Years
ALL
No
Sponsors
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Hospital del Rio Hortega
OTHER
Responsible Party
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Judith Andres
MD
Principal Investigators
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María T Fernandez, MD
Role: STUDY_DIRECTOR
Hospital del Rio Hortega
Locations
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Judith Andres
Valladolid, Castille and León, Spain
Countries
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Other Identifiers
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22-EO132
Identifier Type: -
Identifier Source: org_study_id
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