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Clinical Trials/NCT07286799
NCT07286799
Completed
Not Applicable

Comparison of the Analgesic Efficacy of Posterior Quadratus Lumborum Block and Transversalis Fascia Plane Block in Children Undergoing Orchiopexy

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization1 site in 1 country54 target enrollmentStarted: May 1, 2025Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
Enrollment
54
Locations
1
Primary Endpoint
Time to First Analgesic Requirement After Surgery

Overview

Brief Summary

It was planned to compare the analgesic efficacy of the transversalis fascia plane block and the posterior quadratus lumborum block in children aged 1 to 7 years undergoing orchiopexy, by evaluating their FLACC scores and the time to first postoperative analgesic requirement.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
1 Year to 7 Years (Child)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Children aged 1 to 7 years with ASA physical status I-II undergoing unilateral orchiopexy surgery.

Exclusion Criteria

  • ASA physical status ≥ III
  • History of prematurity (gestational age \< 37 weeks) Known coagulation disorders or bleeding tendency
  • Infection, inflammation, or skin lesion at the injection site
  • Known neurological or neuromuscular diseases
  • Presence of significant cardiac or pulmonary disease (e.g., congenital heart disease, active asthma)
  • Hepatic or renal dysfunction
  • Known allergy or hypersensitivity to local anesthetics (e.g., bupivacaine, lidocaine)
  • Developmental delay or cognitive impairment that prevents accurate pain assessment
  • Use of additional regional analgesia techniques (e.g., caudal block) during surgery
  • Block failure or intraoperative complications requiring exclusion from protocol analysis

Outcomes

Primary Outcomes

Time to First Analgesic Requirement After Surgery

Time Frame: First 24 hours postoperatively

The time elapsed from the end of surgery to the administration of the first rescue analgesic.

Secondary Outcomes

  • FLACC Pain Scores at Specified Time Intervals(First 24 hours postoperatively)

Investigators

Sponsor
Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Reyhan Kucuk Erturk

Resident Doctor

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

Study Sites (1)

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