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The application of colloid volume expansion during induction of general anesthesia in cardiopulmonary bypass surgery

The application of colloid volume expansion during induction of general anesthesia in cardiopulmonary bypass surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-12002832
Enrollment
Unknown
Registered
2012-12-16
Start date
2012-01-20
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

cardiopulmonary bypass surgery

Interventions

volume expansion/fluid liquid:6% hydroxyethyl starch (HES)

Sponsors

First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Select three hundred and ninety-three patients undergoing elective cardiopulmonary bypass cardiac surgery, ASA II or III, cardiac function I - III, age of twenty to sixty years old, conscious, with normal liver and kidney function.

Exclusion criteria

Exclusion criteria: Serious internal environment disorder, asthma, chronic obstructive pulmonary disease, again heart surgery, hearing impairment, mental disorder, cerebral infarction sequelae period.

Design outcomes

Secondary

MeasureTime frame
complications after surgery;mixed venous oxygen saturation (SvO2);—

Primary

MeasureTime frame
length of hospital day after surgery;ventricular end diastolic capacity;SVV(pulse oxygen saturation variation);CO (cardiac output);—

Countries

China

Contacts

Public ContactGu Erwei
ay-guew-mz@yahoo.com.cn+86 13966663478

Outcome results

None listed

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