Viewing Study NCT06417268



Ignite Creation Date: 2024-05-19 @ 5:33 PM
Last Modification Date: 2024-10-26 @ 3:29 PM
Study NCT ID: NCT06417268
Status: RECRUITING
Last Update Posted: 2024-05-16
First Post: 2024-03-20

Brief Title: Combined Pericapsular Nerve Group Block and Lateral Femoral Cutaneous Nerve Block for Pediatric Hip Surgeries
Sponsor: Kasr El Aini Hospital
Organization: Kasr El Aini Hospital

Study Overview

Official Title: Ultrasound-Guided Combined Pericapsular Nerve Group Block and Lateral Femoral Cutaneous Nerve Block Versus Caudal Block for Postoperative Analgesia in Pediatric Hip Surgeries A Randomized Controlled Study
Status: RECRUITING
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: combined pericapsular nerve group PENG block and lateral femoral cutaneous nerve block may be effective in reducing post-operative pain after open hip surgery in children
Detailed Description: All children will be assessed clinically and investigations will be done to exclude the exclusion criteria mentioned above Laboratory works needed complete blood count CBC prothrombin time concentration partial thromboplastin time Midazolam 05mgkg will be given orally to each child in both groups as a premedication half an hour before the procedure

General anesthesia will be induced in a supine position under standard basic monitoring of vital signs with inhalational anesthetic using 100 O2 Sevoflurane

Group C will receive caudal analgesia Bupivacaine 025 at a dose of 1 mlkg Group B will receive PENG block Bupivacaine 025 at a dose of 1 mlkg and lateral femoral cutaneous nerve block Bubivacaine 025 at 01 mlkg

After receiving the block a surgical incision will be done after 15 minutes Continuous recording of heart rate and blood pressure will be carried out from the moment of injection at timely intervals intra-operative Intra-operatively an increase in hemodynamics in response to the skin incision by more than 30 from baseline values 5 min after intubation or thereafter is managed by intravenous administration of fentanyl 1 µgkg to a maximum dose of 2 µgkg Postoperative pain assessment using the FLACC score will then follow for 24 hours

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None