Effects of different examination time on anesthesia demand, intestinal cleanliness and postoperative sleep quality in patients with painless gastroenteroscopy

Status

Recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2400081820

Enrollment

Unknown

Registered

2024-03-13

Start date

2024-03-31

Completion date

Unknown

Last updated

2024-03-18

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

Conditions

Gastrointestinal disease

Interventions

Morning group 8:00 ~12:00:A painless gastroscopy was performed in the morning

Afternoon group 14:00 ~18:00:A painless gastroscopy was performed in the morning

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients presented to our hospital for painless gastroenteroscopy were of all genders, aged 18-65 years, American Society of Anesthesiologists (ASA) grade I or II, BMI 18-25 kg/?, and Malampati airway grade I or II

Exclusion criteria

Exclusion criteria: Sleep disorders, constipation, bowel surgery, intestinal tumors, intestinal bleeding, cardiovascular disease, sleep apnea syndrome, psychosis, history of opioid use, abnormal recovery from surgery or anesthesia, reluctance to provide informed consent, or language difficulties.

Design outcomes

Primary

Measure	Time frame
The dosage of propofol in two groups (mg/kg);Intraoperative intestinal cleanliness;The sleep quality of the two groups was examined;	—

Secondary

Measure	Time frame
Operation time of gastroenteroscopy;hypotension;bradyarrhythmia;hyoxemia;Coughing and moving;nausea and vomiting;Endoscopist and patient satisfaction scores;	—

Countries

China

Contacts

Public Contactdezhi wang

Xi'an Honghui Hospital

84791472@qq.com+86 138 3421 4598

Outcome results

None listed

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