Fasting
Conditions
Interventions
This is an quasi-experimental study, open and non-randomized, with three groups of participants: morning control group – subjected to the traditional preoperative fasting routine performed by the heal
afternoon control group – subjected to the traditional preoperative fasting routine performed by the healthcare unit and surgically approached in the afternoon
and the intervention group – which will receive a drink containing maltodextrin in two periods before surgery (fasting abbreviation protocol): 1st: 6 hours before surgery – 400ml of drink containing m
Sponsors
Hospital Central do Exército
Instituto de Nutrição Josué de Castro/ Universidade Federal do Rio de Janeiro
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Woman from 18 years old; with indication of elective surgery for treatment of breast cancer.
Exclusion criteria
Exclusion criteria: Women with severe gastroesophageal reflux; chronically uncompensated diabetes mellitus; megaesophagus; esophageal and/or intestinal obstruction; gastroparesis; pyloric stenosis and patients with previous gastrointestinal surgery with compromised gastric emptying.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find a reduction in the profile of metabolic and inflammatory markers, verified through blood analyzes of participants who received the intervention, based on the finding of a variation of at least 5% in measurements between control and intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected. | — |
Countries
Brazil
Contacts
Public ContactAndressa Ohana
Hospital Central do Exército
Outcome results
None listed