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A study of comparison between the conventional anatomy based caudal analgesia and ultrasound guided caudal analgesia in paediatric patients undergoing surgeries below the level of umbilicus

A comparative study of ultrasound guided caudal block versus anatomical landmark based caudal block in paediatric patients undergoing infra-umbilical surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/02/040291
Enrollment
150
Registered
2022-02-14
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Realtime Ultrasound Imaging: Caudal block will be given in the selected study population group under real-time ultrasound guidance by experienced anaesthesiologists. Duration of interve

Sponsors

Department of Anaesthesiology IPGMER and SSKM Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a) Patients belonging to either sex of age 1 month to less than 12 years. b) Patients of ASA physical status I and II. c) Patients scheduled to undergo various elective infra-umbilical surgeries

Exclusion criteria

Exclusion criteria: a) Patients aged less than 1 month b) Refusal from parents to give consent for the procedure. c) Patients with evidence of peripheral neuropathy, neurological deficit or motor weakness. d) Patients with significant cardiac, respiratory, hepatic or renal disorders or any other uncontrolled systemic illness e) Bleeding diatheses or history of using anticoagulation medications f) History of pneumothorax g) History of allergy to amide local anaesthetics. h) Infection at the site of needle insertion. i) History of seizures

Design outcomes

Primary

MeasureTime frame
1) proper needle placement 2) no aspiration of blood 3) no aspiration of cerebrospinal fluid 4) no swelling in the sacral regionTimepoint: Outcome will be monitored during performing the procedure. This is not a therapeutic study hence duration of the procedure (from placing the ultrasound probe to placement of the needle in the caudal epidural space) will be considered as time points.

Secondary

MeasureTime frame
An effective caudal analgesia without major hemodynamic alterations and avoiding inadvertent intravascular injection or dural punctureTimepoint: Intraoperative and 30 minutes after the surgery

Countries

India

Contacts

Public ContactDr Maitreyee Mukherjee

IPGMER AND SSKM HOSPITAL, KOLKATA

maitreyee1980.mm@gmail.com9830415924

Outcome results

None listed

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