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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03780790
Other study ID # 2018/1076
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 28, 2018
Est. completion date February 25, 2021

Study information

Verified date March 2022
Source Istanbul University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates analgesic effects of ultrasound-guided (USG) regional anesthetic techniques; caudal block , transversus abdominis plane (TAP) block and quadratus lumborum block (QLB) by comparing postoperative pain scores [ Face, Legs, Activity, Cry, Consolabilty(FLACC) and Visual Analogue Scale (VAS)], first analgesic requirement time and total analgesic consumption in pediatrics undergoing lower abdominal surgery. We also aim to observe the side effects of these techniques such as nausea, vomiting, bradycardia, hypotension, respiratory depression.


Description:

Lower abdominal surgeries affect dermatomes T10-L1 and blocking these nerve roots provides effective postoperative analgesia. Neuroaxial blocks such as epidural and caudal blocks is considered the gold standart regional technique for pain management after lower abdominal surgery, blocking both somatic and visceral pain. Nowadays,US is increasingly used to perform caudal block, demostrating cannule placement and precise deposition of local anesthetic in the epidural space. On the other side truncal blocks as US-guided TAP block covers T10-L1 dermatomes and provides postoperative pain relief after lower abdominal surgery with lower complication rate rather than caudal block but it may not prevent traction on the peritoneal sac. QLB is rather a new regional technique blocking nerve roots close to paravertebral area affecting somatic and visceral nerve fibers. In our study we aim to compare postoperative analgesic effects of these three techniques in paediatrics. Our primary outcomes are pain scores(FLACC/VAS) and first additional analgesic requirement time. Secondary outcomes are total analgesic consumption, side effects (nausea, vomiting, itching, urinary retention, bradycardia, hypotension, respiratory depression), length of hospitalization and chronic pain due to incision after 2 months.


Recruitment information / eligibility

Status Completed
Enrollment 135
Est. completion date February 25, 2021
Est. primary completion date February 1, 2021
Accepts healthy volunteers No
Gender All
Age group 12 Months to 12 Years
Eligibility Inclusion Criteria: - undergoing lower abdominal surgery - ASA(American Society of Anestesiology)1-2 Exclusion Criteria: - denial of patient or parents, - infection on the local anesthetic application area - infection in central nervous system - coagulopathy - brain tumours - known allergy against local anesthetics - anatomical difficulties - with preexisting cardiac dysfunction - with history of renal and/or hepatic dysfunction

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Bupivacaine
% 0,25

Locations

Country Name City State
Turkey Istanbul University Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Istanbul University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Other Incidence of side effects Nausea, vomiting up to 48 hours
Other Incidence of complications Hematoma, dural puncture, infections up to first week
Other Time to first mobilization Time to first mobilization up to 48 hours
Primary Face, Legs Activity, Cry, Consolability (FLACC) scores It includes five categories of behavior, each scored on 0-2 point scale so that total score ranges from 0 to 10. Total scores of 0-3 is defined as mild or no pain, 4-7 as moderate, and 8-10 as severe pain. up to 48 hours
Secondary Hospital stay Hospitalisation Through study completion, an average of 1 week
Secondary Number of patients who require rescue analgesic Number of patients who require IV tramadol (1 mg/kg) at the first 2 hours and parasetamol in the 48 hours up to 48 hours
Secondary First analgesic requirement time Duration of postoperative analgesia Up to 48 hours
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