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Blood Conservation in Patients (3.5-12kg) Undergoing Congenital Cardiac Surgery

Differences in Outcomes for Patients (3.5-12kg) Undergoing Congenital Cardiac Surgery Who Receive Blood Versus Those Who do Not

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05881564
Enrollment
150
Registered
2023-05-31
Start date
2023-05-10
Completion date
2026-05-12
Last updated
2023-06-01

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

Conditions

Congenital Heart Disease

Brief summary

To evaluate if there is any clinical difference in patients 3.5-12kg who undergo cardiac surgery with cardiopulmonary bypass that do and do not receive blood products as part of their procedure. The main hypothesis of the study is that the patients undergoing bloodless cardiac surgery will have decreased morbidity and mortality when compared to the cohort that did receive blood as well as a shorter ICU and hospital length of stay.

Interventions

OTHERblood use for priming cardiopulmonary bypass circuit

one arm will have the cardiopulmonary bypass circuit primed with blood

OTHERclear prime for cardiopulmonary bypass

this arm will not have bypass circuit primed with blood

Sponsors

Augusta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patient weight 3.5-12kg * Elective and urgent cardiac surgery with cardiopulmonary bypass * Cases within the STS STAT categories of 1-4

Exclusion criteria

* Patients who weigh more than 12kg or less than 3.5kg. * Patients undergoing emergency surgery. * STAT category 5 cases. * Patients whose surgery does not require cardiopulmonary bypass. * Patients presenting preoperatively in shock. * Patients with known blood dyscrasias.

Design outcomes

Primary

MeasureTime frameDescription
Number of patients with wound infection in bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 dayswound infection
Number of patients with bleeding requiring reoperation in bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysbleeding requiring reoperation
Number of patients with postoperative pneumothorax in bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 dayspostoperative pneumothorax
Age of patients undergoing bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysage in months
Weight of patients undergoing bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysweight in kg
Gender of patients undergoing bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 dayssex
Demographics of bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysrace
Diagnosis of patients undergoing bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 dayspreoperative diagnosis
Surgery performed in bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 dayssurgery performed
Previous surgery prior to bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysany previous surgery
Blood received during bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysblood product received
Volume transfused during bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysvolume of blood transfusion in mL
Number of patients with unplanned reoperation in bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysunplanned reoperation
Number of patients with unplanned cardiac catheterization in bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysunplanned cardiac catheterization
Number of patients with a neurologic complication in bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysneurologic complication
Number of patients with chylothorax in bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 dayschylothorax
Number of patients with vocal cord injury in bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysvocal cord injury
Number of patients with diaphragm paralysis in bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysdiaphragm paralysis
Number of patients with pacemaker implantation in bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 dayspacemaker implantation
Number of patients with pericardial effusion in bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 dayspericardial effusion
Number of patients who died following bloodless cardiac surgery in patients 3.5-12kg (categorical variable)30 daysmortality

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026