Observational study of s-ketamine combined with propofol in children anesthetized for gastroscopy

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100044321

Enrollment

Unknown

Registered

2021-03-16

Start date

2021-03-14

Completion date

Unknown

Last updated

2021-09-07

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

Conditions

Diseases requiring gastroscopy in children

Interventions

S0 Group:propofol 3mg.kg

S1 Group:s-ketamine 0.3mg.kg

S2 Group:s-ketamine 0.5mg.kg

S3 Group:s-ketamine 0.7mg.kg

Eligibility

Sex/Gender

All

Age

1 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Children aged 1-12 years; 2. Children with ASA grade <=II; 3. No airway abnormalities were found in the children; 4. Children without high risk of regurgitation aspiration.

Exclusion criteria

Exclusion criteria: 1. Children with progressive gastric hemorrhage; 2. Obese children (BMI >35 kg/m2).

Design outcomes

Primary

Measure	Time frame
success rate of gastroscope placement;advesre events after gastroscopy ;	—

Secondary

Measure	Time frame
The amount of propofol be used;	—

Countries

China

Contacts

Public ContactZhang Bin

Qilu Children's Hospital of Shandong University

qletyymzk@sina.com+86 18866115706

Outcome results

None listed

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