FindTrial
Sign In

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

A self-control, single-blind trial: 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-17011021
Enrollment
Unknown
Registered
2017-03-30
Start date
2017-04-10
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

group1, group2:oral preoperative regimens

Sponsors

General Hospital of Guangzhou MilitaryCommand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Aged 18 years and more; 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
time for gastric emptying;glucose;insulin;—

Countries

China

Contacts

Public ContactXiao Guizhen

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