Skip to content

Effect of two hours of fasting on the vital signs, comfort, and safety of patients with painless gastroendoscopy: A randomized controlled trial in China

Experimental study on alleviation of hunger and anxiety in patients with digestive endoscopy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17011022
Enrollment
Unknown
Registered
2017-03-30
Start date
2017-04-01
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

Digestive system disease

Interventions

The control group:The control group of patients was forbidden to drink for 4 h in accordance with the conventional met
The intervention group:The intervention group patients fasting in accordance with traditional methods were assisted by the professionals with their oral administration of 200 ml of 5% glucose 2 h befo

Sponsors

First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Aged between 18 and 65 years; (2) Agreement in participation, both from the patient and its physician; (3) It adopts unified anesthesia, namely, anesthesia ASA grades I–II, during the examination process.

Exclusion criteria

Exclusion criteria: (1) Nasoenteral feeding tube; (2) Unstable clinical condition; (3) Morbid obesity; (4) Active GI bleeding; (5) Speech disorder or mental illness; and (6) Gastroesophageal surgery.

Design outcomes

Primary

MeasureTime frame
vital signs;comfort;

Secondary

MeasureTime frame
safety;gastric mucosal clarity ;

Countries

China

Contacts

Public ContactWang Xiu

Nursing School of Jilin University

wangxiu1649@163.com+86 13756661649

Outcome results

None listed

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