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A clinical study to compare the ultrasound guided caudal block and sacral erector spinal block in paediatric patients undergoing hypospadias repair

Comparison of ultrasound guided caudal block and sacral erector spinae block in paediatric patients undergoing hypospadias repair

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050959
Enrollment
50
Registered
2023-03-22
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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: Ultrasound guided caudal block: In hypospadias patients, After induction of general anaesthesia in a standardized manner, patient will be turned to lateral position for performing cauda

Sponsors

Pt. B.D. Sharma PGIMS Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Paediatric male patients aged 2 to 7 years with American Society of Anesthesiologists (ASA) physical status I or II scheduled to undergo surgery for hypospadias repair will be included in the study .

Exclusion criteria

Exclusion criteria: Patients with :- - history of developmental delay, - allergic reactions to local anaesthetic, -infection at the puncture site -bleeding disorders and on anticoagulants - parental refusal shall not be included in the study.

Design outcomes

Primary

MeasureTime frame
Time for requirement of first rescue analgesic Timepoint: Pain assessment will be done postoperatively using FLACC score at 0 hr, every 15 mins upto 1 hr, every half an hour upto 2 hours, 2 hrly upto 12 hours and then at 18th hour and 24th hour postoperatively

Secondary

MeasureTime frame
1.Total intraoperative fentanyl consumption 2.Post-operative pain score using The Faces Legs Activity Cry Consolability (FLACC) Scale.[15] 3.Post-operative analgesic consumption in 24 hours. 4.Complications, if any[Respiratory depression ,vomiting, others if any, shall be recorded and managed accordingly] Timepoint: Participants will be assessed intially during baseline parameters before induction of general anaesthesia ,before the block, after the block,prior to incision, immediately after the incision and then every 10 minutes till the end of surgery. Total intraoperative fentanyl consumption. Postoperative pain score using the FLACC scale, post operative analgesic consumption in 24 hours.

Countries

India

Contacts

Public ContactDr Praveen kumar R

Pt. B.D. Sharma PGIMS ROHTAK

praveenpkkumar96@gmail.com8903757979

Outcome results

None listed

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