Comparative study of analgesic quality in two methods of bilateral ilioinguinal block and caudal block

Comparative study of analgesic quality in two methods of bilateral illioinguinal block and caudal block with rupivacaine 0.2% in patients aged 3 to 8 years undergoing bilateral inguinal hernia surgery under general anesthesia in the Childern's Medical Center Hospital, 2021-22

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20200521047530N3

Enrollment

Registered

2023-08-25

Start date

2021-06-22

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

Bilateral inguinal hernia surgery.

Interventions

Intervention 1: Intervention group 1: Patient under bilateral ilioinguinal block with rupivacaine 0.2%( manufactured by MOLTENI farmaceutici) under ultrasound guide. After determining the sedation sco

Eligibility

Sex/Gender

All

Age

3 Years to 8 Years

Inclusion criteria

Inclusion criteria: All children from 3 to 8 years old Candidate for bilateral inguinal hernia surgery Under general anesthesia ASA class 1 and 2

Exclusion criteria

Exclusion criteria: Allergy to local anesthetics Non-Persian speaking patients Sacral infection Coagulation disorders History of seizures Weight more than 20 kg Patients who are being treated with a variety of painkillers and psychiatric medications for any reason

Design outcomes

Primary

Measure	Time frame
Pain score based on CHEOPS criteria. Timepoint: After the patient enters the recovery ward, the pain score is recorded. Method of measurement: Children's Hospital of Eastern Ontario Pain Scale.;PAED Delirium Score. Timepoint: After the patient enters the recovery ward, it is recorded. Method of measurement: It is obtained based on The Pediatric Anesthesia Emergence Delirium criteria.	—

Secondary

Measure	Time frame
Recovery time. Timepoint: It is recorded and calculated between the time the patient enters the recovery ward and the patient leaves it. Method of measurement: It is recorded and calculated between the time the patient enters the recovery ward and the patient leaves it.;Need for additional drugs (fentanyl). Timepoint: Additional dose of fentanyl prescribed after surgical incision or in the recovery ward. Method of measurement: Additional dose of fentanyl prescribed after surgical incision or in the recovery ward in micrograms per kilogram.	—

Measure

Time frame

Recovery time. Timepoint: It is recorded and calculated between the time the patient enters the recovery ward and the patient leaves it. Method of measurement: It is recorded and calculated between the time the patient enters the recovery ward and the patient leaves it.;Need for additional drugs (fentanyl). Timepoint: Additional dose of fentanyl prescribed after surgical incision or in the recovery ward. Method of measurement: Additional dose of fentanyl prescribed after surgical incision or in the recovery ward in micrograms per kilogram.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactNima Nazari

Tehran University of Medical Sciences

n-nazari@sina.tums.ac.ir00982161479

Outcome results

None listed

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