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Influence of EndoAngel on comfort medical treatment of patients undergoing painless gastrointestinal endoscopy

Influence of EndoAngel on comfort medical treatment of patients undergoing painless gastrointestinal endoscopy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042621
Enrollment
Unknown
Registered
2021-01-24
Start date
2021-01-25
Completion date
Unknown
Last updated
2021-05-10

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

Conditions

Disease of digestive tract

Interventions

Control group:The control group underwent routine painless gastroscopy
Experimental group:The experimental group underwent painless gastroscopy with the assistance of artificial intelligence system

Sponsors

Renmin Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Aged between 18 and 65 years old (included); 2) Painless gastroscopy should be performed to further clarify the characteristics of digestive tract diseases; 3) Able to read, understand and sign informed consent.

Exclusion criteria

Exclusion criteria: 1) The subject meets the contraindications for gastrointestinal endoscopy; 2) High-risk patient sassessed by the anesthesiologists that not suitable for undergoing painless gastroscopy, including cardiovascular and cerebrovascular diseases, systemic basic diseases, etc.; 3) Patients with vertigo; 4) Asthma; 5) Anesthetics allergy; 6) Known active upper gastrointestinal bleeding or emergency gastroscopy; 7) Pregnant women; 8) Gastric retention, pyloric obstruction; 9) High-risk diseases or other special conditions that the reaearchers consider the subject unsuitable for participation in the clinical trial.

Design outcomes

Primary

MeasureTime frame
Time of recovery from anesthesia;Recovery time;Patient satisfaction score (5-Point Likert Scale);

Secondary

MeasureTime frame
Anesthesia induction time of 2 groups;Examination time;Intraoperative dosage of propofol;In the observation group, heart rate, systolic blood pressure, pulse oxygen saturation and respiration (fluctuation of vital signs: blood pressure and heart rate) were observed at T0 (baseline), T1 (entry), T2 (5min of operation), T3 (10min of operation), T4 (exit) and T5 (completion of operation).;Visual analogue pain score (VAS) at 5, 15, 30, 45 and 60min after waking up in 2 groups;Ramsay sedation score;Anesthesiologist Satisfaction (5-Point Likert Scale);Satisfaction of endoscopic doctors (5-point Likert scale);Incidence of intraoperative adverse reactions;Incidence of postoperative adverse reactions;Incidence of postoperative adverse reactions;

Countries

China

Contacts

Public ContactYu Honggang

Renmin Hospital of Wuhan University

yuhonggang1968@163.com+86 13871281899

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026