prospective study
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ASA I, II
Exclusion criteria
Exclusion criteria: coagulopathies, infection at the block targeted site, or with known allergy to any of the drugs included in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the duration of the postoperative caudal analgesia and severity of postoperative pain | — |
Secondary
| Measure | Time frame |
|---|---|
| Number of rescue analgesic doses, residual motor block, and side effects like nausea and vomiting | — |
Countries
Africa
Contacts
Minya University, Faculty of medicine anesthesia and intensive care department