An observational study of the effect on volume response indicators by general anesthesia

An observational study of the effect in general anesthesia on volume response indicators

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100051796

Enrollment

Unknown

Registered

2021-10-04

Start date

2021-10-01

Completion date

Unknown

Last updated

2022-10-04

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

Conditions

General anesthesia

Interventions

Children group:No

Adults group:No

Eligibility

Sex/Gender

All

Age

1 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective general anesthesia (ASA I-II); 2. 120 subjects in the children group, aged 1-10 years; and 120 subjects in the adult group, aged >18 years; 3. Sign the informed consent form, promise to abide by the research procedures and cooperate with the implementation of the whole process of research.

Exclusion criteria

Exclusion criteria: 1. Emergency surgery patients; 2. Complications of heart, lung, liver and kidney; 3. Cyclic instability.

Design outcomes

Primary

Measure	Time frame
Aortic peak flow velocity variability;Aortic velocity time integral variability;SV (stroke volume);	—

Secondary

Measure	Time frame
Hemodynamic indexes;	—

Countries

China

Contacts

Public ContactYang Lijun

Fujian Maternity and Child Health Hospital; Affiliated Hospital of Fujian Medical University

yy00633@126.com+86 17805949907

Outcome results

None listed

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