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Recruiting Not applicable NCT07540689

The Analgesic Efficacy of M-TAPA for Laparoscopic Abdominal Surgery in Children

No applicable phase (e.g. observational)
Conditions: Post Operative Pain

Sponsor: Kasr El Aini Hospital

trial.available_in: БГ
Overview
This investigation aims to assess the efficacy of M-TAPA in children undergoing laparoscopic abdominal surgery. Sixty pediatric patients undergoing laparoscopic abdominal surgery under general anesthesia will be enrolled in this single-center study. Preoperatively, participants will be randomly assigned to receive either port-site local anesthetic infiltration or M-TAPA.
Description
This investigation aims to assess the efficacy of M-TAPA in children undergoing laparoscopic abdominal surgery. Sixty pediatric patients undergoing laparoscopic abdominal surgery under general anesthesia will be enrolled in this single-center study. Preoperatively, participants will be randomly assigned to a port site local anesthetic infiltration. or M-TAPA. 1. port-site local anesthetic infiltration Before the skin incision, the surgeon will inject 0.17 mL/kg of 0.25% bupivacaine (up to 2 mg/kg) via infiltration into the skin, subcutaneous tissue, and muscle fascia at the three laparoscopic ports. 2. M-TAPA. Before skin incision, Ultrasound will be used to perform bilateral M-TAPA.0.25 mL/kg of 0.25% bupivacaine will be administered at each side.
Who can participate
Inclusion Criteria: * Age (1-7) years. * Both genders. * American Society of Anaesthesiologists (ASA) - physical status I-II. * Children undergoing elective laparoscopic abdominal surgery. Exclusion Criteria: * Parental refusal. * Bleeding disorders with INR \> 1.5 and/or platelets \< 50 000. * History of allergic reactions to local anesthetics. * Rash or signs of infection at the injection site.
Interventions
port site infiltration
PROCEDURE
M-TAPA
PROCEDURE
Locations 1
Egypt (1)
Kasralainy Hospital
Cairo , Elmanial
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
1 Year
Maximum age
7 Years
Healthy volunteers
No
Start date
01.05.2026
Completion date
01.04.2027
Registry ID
NCT07540689
Source
clinicaltrials.gov
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