Study on the clinical effect of improved anesthesia induction method for emergency patients at risk of aspiration

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100046933

Enrollment

Unknown

Registered

2021-05-31

Start date

2021-07-01

Completion date

Unknown

Last updated

2022-01-10

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

Conditions

None listed

Interventions

Group 1:Improved induction

Group 2:Traditional inducement

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. No gender limit; 3. The subject voluntarily participates in the study and has signed an informed consent form; 4. Meet one of the following conditions: (1) Emergency surgery diagnosed as acute gastrointestinal obstruction (within 4h after meal); (2) Emergency surgery within 3 hours after a normal meal.

Exclusion criteria

Exclusion criteria: 1. The patient is unconscious; 2. The patient has had reflux aspiration before the operation; 3. Other circumstances in which the patient is judged to be unsuitable to participate in the clinical trial.

Design outcomes

Primary

Measure	Time frame
reflux and aspiration;artificial assisted breathing;place the stomach tube;	—

Secondary

Measure	Time frame
mean arterial pressure;heart rate;pulse oximetry;blood gas result;subjective feelings;bad memory;fate;	—

Countries

China

Contacts

Public ContactQian Bin

985578655@qq.com+86 13951489138

Outcome results