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NCT04830280 Clinical Trial

Effect Posterior QLB on Atelectasis

Pediatrics Clinical Trial

Official title:
The Effect of Ultrasound-guided Posterior Quadratus Lumborum Block on Atelectasis in Pediatric Patients

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04830280
Other study ID # 2021/03-11
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 1, 2021
Est. completion date September 30, 2021

Study information
Verified date June 2021
Source Zonguldak Bulent Ecevit University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

We aimed to investigate the effect of posterior quadratus lumborum block on postoperative atelectasis in inguinal hernia surgery in pediatric patients.

Recruitment information / eligibility
Status Recruiting
Enrollment 2
Est. completion date September 30, 2021
Est. primary completion date August 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A to 2 Years
Eligibility Inclusion Criteria: - under 2 years old, - ASA I-II risk group - Patients who underwent an inguinal hernia operation under general anesthesia, posterior quadratus lumborum block for postoperative analgesia or pain treatment with conventional method - Patients whose informed consent was read and approval was obtained from him and his guardian Exclusion Criteria: - who do not want to participate in the study, - ASA III-IV-V patients

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• posterior quadratus lumborum block
administration local anesthetic solution between the middle layer of the thoracolumbar fascia and QL muscle at the posterior edge of the quadratus lumborum muscle

Locations
Country Name City State
Turkey Zonguldak Bülent Ecevit University Medicine Faculty Zonguldak Kozlu

Sponsors (1)
Lead Sponsor Collaborator
Zonguldak Bulent Ecevit University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary lung ultrasound score atelectasis up to 1 hour after surgery
Secondary pain scores Flacc scores up to 6 hour after surgery
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