Skip to content

A Clinical trial to Compare the Pain reducing ability of Caudal Block with Multiple Injection Costotransverse Block in children undergoing renal surgery.

Comparison of Caudal epidural block with Multiple injection Costotransverse block for renal surgeries in paediatric patients: A prospective randomised, blinded clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/05/042639
Enrollment
56
Registered
2022-05-18
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N25-N29- Other disorders of kidney and ureter

Interventions

Intervention1: Group MICB: Ultrasound guided Multiple Injection Costotransverse Block (MICB) : Group MICB: Ultrasound guided Multiple Injection Costotransverse Block with ropivacaine (0.2%) 2mg/kg. L

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age-6months to 7years of age 2. American Society of Anaesthesiology (ASA) physical status- I & II 3. Paediatric renal surgeries

Exclusion criteria

Exclusion criteria: 1. Refusal by parents or guardians to participate in the study 2. Developmental delay and mental retardation 3. Coagulopathy 4. Infection at the puncture site 5. Significant cardiac, renal and liver diseases 6. Obesity

Design outcomes

Primary

MeasureTime frame
Comparing both the blocks and to find out the effective block amongst the two, by comparing Total fentanyl requirement post-surgery for 24 hours.Timepoint: 24hrs post surgery

Secondary

MeasureTime frame
Parental satisfaction scoreTimepoint: At the end of 24 hours ;Analgesic consumption at different time intervalsTimepoint: post operative period (0-6 hrs,6-12 hrs,12-24 hrs);Assessment of preoperative anxiety by Modified Yale Preoperative Anxiety Scale Timepoint: Before premedication in pre operative holding area and before induction of anaesthesia in ot;Comparing the post operative pain by FLACC scoreTimepoint: postoperative period (0 minutes, 30 minutes, 1st hour, 2nd hour, 4th hour, 6th hour, 12th and 24th hour);Complications like Vomiting, urinary retention and lower limb motor weakness using Modified Bromage ScaleTimepoint: postoperative period (0 minutes, 30 minutes, 1st hour, 2nd hour, 4th hour, 6th hour, 12th and 24th hour) ;Duration of analgesia - Time to first dose of analgesic (rescue analgesic - fentanyl)Timepoint: postoperative period (0 minutes, 30 minutes, 1st hour, 2nd hour, 4th hour, 6th hour, 12th and 24th hour);Hemodynamic changes (SBP, DBP, MAP and HR) Timepoint: Intraoperative period (every 10 mins) and postoperative period (0 minutes, 30 minutes, 1st hour, 2nd hour, 4th hour, 6th hour, 12th and 24th hour)

Countries

India

Contacts

Public ContactMeenakshi Sundharesan A

All India Institute of Medical Sciences, New Delhi

debeshbhoi@gmail.com7042129428

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026