Transversalis Fascia Plane Block in Pediatric Patients

Not Applicable

Active, not recruiting

• Conditions: Parental Satisfaction; Regional Anesthesia; Pain, Postoperative
• Interventions: Procedure: Transversalis Fascia Plane Block

• Registration Number: NCT06391528
• Lead Sponsor: Zonguldak Bulent Ecevit University

Brief Summary

to investigate the effects of Transversalis Fascia Plan Block after induction of anesthesia on perioperative opioid consumption, hemodynamic changes, postoperative FLACC pediatric pain score, non-opioid analgesic use and parental satisfaction in pediatric patients undergoing unilateral inguinal hernia or undescended testicular repair under general anesthesia.

Detailed Description

Not available

Study Timeline

• Status Verified: 2024-04
• Study Start: 2024-04-01
• Study First Submitted: 2024-04-26
• Study First Submitted QC: 2024-04-26
• Last Update Submitted: 2024-04-26
• Study First Posted: 2024-04-30
• Last Update Posted: 2024-04-30
• Primary Completion: 2025-04-30
• Study Completion: 2025-06-30

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• 1-9 years old
• ASA I-II risk group
• Patients whose consent was obtained from their parents with an informed consent form
• Patients who will undergo Inguinal Hernia or Undescended Testi

Exclusion Criteria

• ASA >2
• History of allergy to local anesthetics
• Known coagulation disorders
• Infection near the entry site
• Body mass index >30
• Those whose parents refused to participate in the study
• Those contraindicated for regional anesthesia
• Those with neurological or neuromuscular disease
• Patients with psychiatric problems
• Patients with a history of opioid use
• Chronic analgesic use
• Operation duration exceeding 2 hours

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group FTB	Transversalis Fascia Plane Block	-

Primary Outcome Measures

Name	Time	Method
postoperative pain scores	up to 24 hour after surgery	Patients will be evaluated at regular intervals after surgery and their pain will be measured using a FLACC scores.

Secondary Outcome Measures

Name	Time	Method
parental satisfaction	during the procedure	asking parents about their satisfaction

Trial Locations

Locations (1)

Zonguldak Bülent Ecevit University medicine faculty; 🇹🇷 Zonguldak, Kozlu, Turkey