A prospective and randomized clinical study on the evaluation of the recovery of infants after cardiopulmonary bypass with different levels of colloidal osmotic pressure

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000030284

Enrollment

Unknown

Registered

2020-02-27

Start date

2020-03-01

Completion date

Unknown

Last updated

2020-03-02

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

Conditions

Congenital heart disease

Interventions

A:maintain COP 18mmHg

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Weight less than 5kg; 2. Preoperative liver and kidney function is normal; 3. Normal coagulation function, and did no take drugs that affect the coagulation function; 4. Preoperative data were complete.

Exclusion criteria

Exclusion criteria: 1. Emergency or secondary surgery; 2. Palliative surgery; 3. Hemodynamic instability or emergency surgery; 4. Intraoperative hemorrhage and other surgical accidents; 5. Serious infection.

Design outcomes

Primary

Measure	Time frame
Colloidal osmotic pressure;	—

Countries

China

Contacts

Public ContactPeicheng Ding

Children's Hospital Affiliated to Nanjing Medical University

670811252@qq.com+86 15195807955

Outcome results

None listed

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