Acute pain. Acute pain
Conditions
Interventions
Placebo
Intervention 1: In the intervention group, patients received 5 ml/kg of 12.5% CHO solution two hours before surgery. Intervention 2: In the control group, patients received 5 ml/kg of plain water two
Treatment - Drugs
In the intervention group, patients received 5 ml/kg of 12.5% CHO solution two hours before surgery.
In the control group, patients received 5 ml/kg of plain water two hours before surgery.
Sponsors
Vice Chancellor for Research & Technology, Kashan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
6 Years to 16 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Age 6-16 years old ;elective unilateral herniorrhaphy; Exclusion Criteria: history of diabetes; autoimmune disease; use of non-steroidal analgesics drugs
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: 2-6-12-24 hours. Method of measurement: Visual Analog Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Nausea and vomiting. Timepoint: 2-6-12-24 hours. Method of measurement: Number of cases occurred. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Reza Fazel
Kashan University of Medical Sciences
Outcome results
None listed