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A real world study for painless gastroscopy therapy

A real world study for painless gastroscopy therapy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000031892
Enrollment
Unknown
Registered
2020-04-13
Start date
2019-10-01
Completion date
Unknown
Last updated
2020-04-20

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

Conditions

Gastrointestinal diseases

Interventions

laryngeal mask group VS tracheal intubation group:no intervention

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. all the patients received painless gastroscopy(including normal, fat, aged person); 2. surgery duration will not be more than 3 hours; 3. age>=18 years old.

Exclusion criteria

Exclusion criteria: 1. Can't obtain informed consent form; 2. the patient will be suitable to only laryngeal mask or tracheal intubation, that will bring in method bias; 3. patient mouth can't open more than 2.5cm or have cervical spondylosis; 4. be upper respiratory tract infection within 10 days; 5. be high risk of regurgitation and aspiration; 6. surgery duration will be more than 3 hours.

Design outcomes

Primary

MeasureTime frame
success rate of endoscopic insertion;

Secondary

MeasureTime frame
total time of trying to install mask or intubation to successfully keep airway open;how many times try to insert mask or intubation till success;dosage of propofol in surgery;Degree of airway damage after surgery;

Countries

China

Contacts

Public ContactYunqi Lv

The First Affiliated Hospital of Zhengzhou University

lyq260703@163.com+86 13939019005

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026