Postoperative complications
Conditions
Interventions
The population studied will be subdivided into two groups: intervention and control, through randomization stratified by type of surgery. The CHO group is called light tea with 12.5% maltodextrin and
Dietary supplement
SP6.051.227
Sponsors
Instituto Nacional de Câncer
Instituto Nacional de Câncer
Eligibility
Age
19 Years to 99 Years
Inclusion criteria
Inclusion criteria: All patients who are candidates for elective surgeries; who are 19 years of age or older; and consent to participate in the study through the signing of the Informed Consent Form.
Exclusion criteria
Exclusion criteria: Volunteers inability to receive oral feeding in the preoperative period; without adherence to any of the phases of the study protocol; in use of prophylactic antiemetics 24 hours before surgery and in the immediate postoperative period; with previous diagnosis of diabetes mellitus, chronic kidney disease and / or liver disease, obesity (WHO, 2000); with presence of gastroesophageal reflux; intestinal obstruction and cases of gastroparesis and / or pyloric stenosis and surgeries with low nutritional impact (base of skull, maxillary sinuses, thyroid gland, parotid glands, cutaneous and ocular).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Increased muscle strength in the group receiving CHO-P, compared to the CHO group, around 10% higher, verified by assessment of palmar grip strength. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 1: Reduction in response to insulin resistance, measured by the HOMA-IR and QUICKI indices, more effective in the CHO-P group with a difference of p <0.05 in relation to the CHO group. Expected outcome 2: Lower incidence of postoperative complications, assessed by self-collected data sheet, in the CHO-P group compared to the CHO group. There is no expected reduction parameter. | — |
Countries
Brazil
Contacts
Public ContactLeonardo Murad
Instituto Nacional de Câncer
Outcome results
None listed