Erector Spinae Plane Block for Peroperative Analgesia and Intraabdominal Tissue Oxygenation (NCT03808129) | Clinical Trial Compass
CompletedNot Applicable
Erector Spinae Plane Block for Peroperative Analgesia and Intraabdominal Tissue Oxygenation
Turkey (Türkiye)49 participantsStarted 2019-01-18
Plain-language summary
Brief summary: Regional anesthesia decreases the need for intravenous analgesia in the peri-operative period. Erector spinae plane (ESP) is a regional anesthesia technique shown to be effective at the dorsal and ventral rami of the thoracic spinal nerve along with sympathetic nerve fibers. The purpose is to demonstrate the contribution of ESP block to the postoperative analgesia by ultrasonography and to increase intraabdominal tissue oxygenation compared to the control group.
Who can participate
Age range
6 Months – 2 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Children aged 6 months to 2 years
. According to American Anesthesia Society Anesthesia Risk Scale ASA I-II class patients
. Patients with lower abdominal surgery
Exclusion criteria
. Children under 6 months and older than 2 years
. According to American Anesthesia Society Anesthesia Risk Scale Patients with ASA III-IV class
. Patients with contraindication to regional anesthesia
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
FLACC scale
Timeframe: From recovery of anesthesia to end of study ( postoperative 24 hours)
2
NIRS
Timeframe: Before anesthesia induction to end of operation ( intraoperative 2 hours )