inguinal hernia
Conditions
Interventions
1.Term: From the induction of anesthesia to discharge, and following 24hours at home. 2.Dose: Total dose is given to one layer. 3.Times: Once
1.Term: From the induction of anesthesia to discharge,
Sponsors
Tokyo Metropolitan Children's Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Patients who undergo scheduled inguinal hernioplasty as outpatient. 2.ASA physical status 1 or 2. 3.Patients whose guardians agree with participation of the study and sign the agreement form.
Exclusion criteria
Exclusion criteria: 1.Patients who have surgical or traumatic scars in abdominal wall. 2.Patients who undergo both sides hernioplasty in the same day 3.Patients who are not appropriate to receive surgery as out patients 4.Patients who are not appropriate for the study judged by the primary researcher
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary aim was to evaluate postoperative analgesia as the FLACC score at 45minutes after surgery and the requirement for other analgesics in recovery room and at home | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) the requirement for other analgesics in recovery room and at home within 24hours after surgery 2) evaluate the immediate effect of the II/IH nerve block on body movement at the incision site | — |
Countries
Japan
Contacts
Public ContactNoriko Miyazawa
Tokyo Metropolitan Children's Medical Center Anesthesiology
Outcome results
None listed