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Effects of perioperative glucose supplementation on postoperative nausea and vomiting and postoperative delirium in patients undergoing endoscopic surgery

Effects of perioperative glucose supplementation on postoperative nausea and vomiting and postoperative delirium in patients undergoing endoscopic surgery

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039285
Enrollment
Unknown
Registered
2020-10-22
Start date
2020-11-30
Completion date
Unknown
Last updated
2021-01-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Perioperative management

Interventions

Oral glucose group:Oral 5% glucose solution 5ml/kg 2 h before operation (<=400ml)
Intravenous glucose group:After anesthesia - induced intubation, 250ml 5% glucose solution was administered intravenously

Sponsors

The First Affiliated Hospital of Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 50-70 years; 2. ASA I-II; 3. The anesthesia time for the patients with the estimated operation time of 1-3 hours during daytime endoscopic surgery is 2-4 hours; 4. Patients with no history of allergy to narcotic drugs; 5. Patients without dyspnea or contraindications for intubation or LMA use; 6. Patients without mental disorder and related history; 7. Patients who were not operated for the second time in recent 3 months; 8. Patients who voluntarily entered the clinical trial.

Exclusion criteria

Exclusion criteria: 1. Patients with fasting blood glucose more than 6.1mmol/l or diabetes history; 2. Patients with important organ diseases or endocrine disorders; 3. Patients who received antiemetic or steroid therapy before operation; 4. Patients who have recently used drugs that affect glucose metabolism and insulin secretion; 5. The object of pregnancy; 6. Subjects with history of taking psychotropic drugs or definite history of mental illness; 7. Subjects with a history of alcohol abuse or drug dependence; 8. Subjects with history of POCD, cerebral organic disease or cerebrovascular accident; 9. Those who have been educated for less than 6 years; 10. People who are unable to communicate, such as impaired visual and auditory perception, language disorder, severe dementia or coma; 11. The subjects with positive cam score before operation.

Design outcomes

Primary

MeasureTime frame
Incidence of PONV;Incidence of postoperative delirium;

Secondary

MeasureTime frame
Blood ketone;blood glucose;

Countries

China

Contacts

Public ContactWang Yuelan/ SunYongtao

The First Affiliated Hospital of Shandong First Medical University

wyldgf@163.c0m+86 15953105780; +86 18660795201

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026