Nausea and vomiting
Conditions
Interventions
Randomised double blind controlled trial
Group 1: Children will receive 20 ml/kg of IV compound sodium lactate solution intra-operatively
Group 2: Children will receive no intravenous fluid intra-op
Sponsors
Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 300 children between 2 and 12 years
Exclusion criteria
Exclusion criteria: Does not match inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of nausea and vomiting | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United Kingdom
Outcome results
None listed