None listed
Conditions
Interventions
Procedure/Surgery : ? All subjects with diabetes are randomly assigned to either the intervention group or the control group after receiving an explanation of the study and signing the consent form th
Nucare NoNPO®
Daesang Wellife, Seoul, Korea) three hours before the surgery starts.
? Both groups manage their blood glucose levels using the modified Albert protocol during the fasting periods before and after th
Sponsors
Samsung Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: ASA class II-III adult patients (ages 19 - 69) Patients undergoing gynecological surgery via laparoscopy Patients diagnosed with diabetes mellitus before surgery
Exclusion criteria
Exclusion criteria: 1) Children (< 19 years of age) 2) Elderly (= 70 years) 3) Pregnant and nursing mothers 4) Patients with unstable vital signs 5) Patients at high risk of pulmonary aspiration 6) Individuals taking medications that can affect gastrointestinal motility (opioids, antispasmodics) 7) Patients receiving enteral tube nutrition 8) Emergency surgery 9) Patients who do not consent to participate in the study 10) Patients with liver or kidney disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Gastric fluid volume;Gastric fluid acidity | — |
Secondary
| Measure | Time frame |
|---|---|
| Pre-, Peri-, Post-operative glucose level; Patient's hunger, thirst, and anxiety levels;Insulin resistance;Degree of recovery; Recovery of bowel function (time to first flatus); Postoperative recovery satisfaction;Cortisol level;CRP level;Postoperative complication | — |
Countries
Korea, Republic of
Contacts
Public ContactYu Jeong Bang
Samsung Medical Center
Outcome results
None listed