Comparison of the postoperative analgesia between the caudal and ilioinguinal/ iliohypogastric blocks

Phase 3

Recruiting

Conditions: Postoperative pain.
Acute postoperative pain, not elsewhere classified
MG31.2

Registration Number: IRCT20170516033992N11

Lead Sponsor: Oroumia University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 60

Inclusion Criteria

Patients with physical status equal to or greater than two according to the criteria of the American Anesthesia Association (II>ASA)
Aged between 6 months and 5 years
Not having a spinal deformity

Exclusion Criteria

Coagulation problems such as hemophilia, DIC
Severe infections such as septicemia, meningitis
Brain tumors with increased intracranial pressure
Allergy to local anesthetics
Chemotherapy with drugs such as cisplatin
Hypovolemia
Skin or subcutaneous lesions like infection, angioma at the puncture site

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain score. Timepoint: in recovery, 6, 12 and 24 hours after surgery. Method of measurement: Face, Legs, Activity, Cry, Consolability (FLACC) pain scale.;Prescribing an analgesic. Timepoint: after surgery. Method of measurement: yes/no.;The time of the first request for an analgesic. Timepoint: after surgery. Method of measurement: Minute.

Secondary Outcome Measures

Name	Time	Method
Hart rate. Timepoint: In recovery, 6, 12 and 24 hours after surgery. Method of measurement: Monitoring.;Systolic blood pressure. Timepoint: In recovery, 6, 12 and 24 hours after surgery. Method of measurement: Monitoring.;Diastolic blood pressure. Timepoint: In recovery, 6, 12 and 24 hours after surgery. Method of measurement: Monitoring.;Nausea and vomiting. Timepoint: After surgery. Method of measurement: yes/no.