Ultrasound Guided Posterior Versus Lateral Transversus Abdominis Plan Block for Prolonged Postoperative Analgesic Effect in Children

Pain, Postoperative Clinical Trial

Official title:

Ultrasound Guided Posterior Versus Lateral Transversus Abdominis Plan Block for Prolonged Postoperative Analgesic Effect in Children . Randomized Controlled Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04049838
• Other study ID #: 011223456
• Status: Recruiting
• Phase: N/A
• Start date: February 16, 2019
• Est. completion date: December 5, 2019

Study information

• Verified date: October 2019
• Source: Kasr El Aini Hospital
• Contact: Mohamed M Kamel, MD
• Phone: 01005238534
• Email: mohamedmaher959[@]yahoo.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Ultrasound Guided Posterior Versus Lateral Transversus Abdominis Plan Block for Prolonged Postoperative Analgesic Effect in Children

Description:

the investigators will compare the effect of posterior Transversus abdominis plan block versus the effect of lateral transversus abdominis plan bock regarding the duration of analgesia and patients satisfaction the study will be conducted on 69 children aged from 1 to 7 years presented for lower abdominal surgery.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 69
• Est. completion date: December 5, 2019
• Est. primary completion date: November 5, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 1 Year to 7 Years

Eligibility

Inclusion Criteria:

• children from 1- 7 years

• scheduled to undergo lower abdominal surgery

Exclusion Criteria:

• bleeding disorders

• emergency surgery

• skin lesion at site of needle insertion

Related Conditions & MeSH terms

• Pain, Postoperative

Intervention

Procedure:
• postoperative analgesia for lower abdominal surgery in children
compare lateral and posterior approaches of trannsversus abdominis plane block for analgesia after lower abdominal surgery in children

Locations

Country	Name	City	State
Egypt	Kasr Al Aini	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Kasr El Aini Hospital

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	postoperative pain assessment by the CHEOPS score	Children's Hospital of Eastern Ontario Pain Scale (CHEOPS) for Post-Op Pediatric Pain the score is based on 6 crtiteria: crying; facial expression; child verbal expression; body positiion; touching or grabbing at wound; legs position criterion 1 is given a score of 1-3, criterion 2 and 3 are given score 0-2, criterion 4,5 and 6 are given a score 1-2 making the worst possible score 13 while the least possible score is 4.; a total score of 6 or less indicates adequate analgesia	the first 24 hours postoperative
Secondary	heart rate	Measurement of heart rate (beats per minute)	at 2,4,8,12 and 24 hours postoperative
Secondary	Mean arterial blood pressure	Measurement of Mean arterial blood pressure ( mm Hg)	at 2,4,8,12 and 24 hours postoperative