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A self-control, single-blind trial: The effect of oral preoperative regimens on gastric emptying

The effect of oral preoperative regimens on gastric emptying in healthy adults

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-16009559
Enrollment
Unknown
Registered
2016-10-23
Start date
2016-10-08
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

surgery

Interventions

Case series:oral preoperative regimens

Sponsors

General Hospital of Guangzhou MilitaryCommand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 60 years; 2. BMI 18.5 kg/m2 to 23.5 kg/m2; 3. The written informed consents were obtained after being fully informed of its goal and methots.

Exclusion criteria

Exclusion criteria: 1. Have diabetes (2014 ADA); 2. gastrointestinal disease/surgery; 3. have endocrine disease: thyroid, pituitary, parathyroid gland or adrenal lesions; 4. risk of aspiration, gastroplegia; 5. liver disfunction (AST, ALT more than normal); 6. kidney disfunction (BUN, Cr more than normal); 7. using hormones or medicine of gastric emptying in 1 week; 8. pregnancy or lactation women; 9. Researchers think that doesn't fit in any situation of this study.

Design outcomes

Primary

MeasureTime frame
Gastric emptying;—

Secondary

MeasureTime frame
glucose;insulin;—

Countries

China

Contacts

Public ContactXiao Guizhen

Department of Nutrition, General Hospital of Guangzhou Military Command

gzjane999@163.com+86 020-88653440

Outcome results

None listed

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