Individualized Strategies of Red Blood Cell Transfusion for Perioperative Pediatric Patients

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000037876

Enrollment

Unknown

Registered

2020-09-02

Start date

2021-03-01

Completion date

Unknown

Last updated

2020-11-09

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

Conditions

Perioperative anemia

Interventions

control group:The transfusion is triggered and the volume of the transfusion is estimated according to current guidelines and clinical practice.

study group:According to the oxygen supply / oxygen consumption balance scale, the timing and volume of blood transfusion were determined.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients with age > 1 month; 2. Surgical children; 3. Patients with preoperative 7 g / dl < HB < 10 g / dl, or estimated HB < 10 g / dl during operation.

Exclusion criteria

Exclusion criteria: 1. Patients with bleeding and coagulation diseases; 2. Newborns or premature infants; 3. Children with cyanotic congenital heart disease; 4. Patients with ischemic heart disease or ischemic cerebrovascular disease; 5. Patients whose family members disagree.

Design outcomes

Primary

Measure	Time frame
the volume of red blood cell (RBC) used adjusted to body weight;	—

Secondary

Measure	Time frame
Hb;length of stay in post anesthesia care unit (PACU);unexpected transfer to intense care unit (ICU);length of stay in hospital after operation;the number of patients who need RBC transfusion;	—

Countries

China

Contacts

Public ContactYun Shi

Shanghai Fudan University Affiliated pediatric hospital

imulashi@yahoo.com+86 13918268351

Outcome results

None listed

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