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Effect of Retrograde Autologous Blood Priming on Pulmonary Mechanics in Pediatric Cardiac Surgery (RAPCPB)

A

Ain Shams University

Status

Completed

Conditions

Congenital Heart Disease

Treatments

Procedure: Pediatric cardiac surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT04260204
ACTS004367

Details and patient eligibility

About

The present study hypothesized that beyond its hemodynamic affects,retrograde autologus blood priming of cardiopulmonary bypass (RAP) has a positive impact on hemodynamics and pulmonary mechanics subjected to cardiac surgery.

Full description

This prospective randomized study analyzed the clinical records of 124 children subjected to cardiac surgery for congenital heart diseases with left to right shunt. They comprised 64 patients with RAP and 60 patients conventional cardiopulmonary bypass priming. The preoperative, intraoperative and postoperative data of the studied patients were reported.

Enrollment

124 patients

Sex

All

Ages

12 months to 5 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • children complained of congenital heart disease with left to right shunt pressure or volume load

Exclusion criteria

  • cyanotic heart disease

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

124 participants in 2 patient groups

Retrograde priming
Active Comparator group
Description:
retrograde autologous Blood Priming of Cardiopulmonary Bypass (RAP) in young children subjected to cardiac surgery for congenital heart defects with left to right shunt associated with volume or pressure overload.
Treatment:
Procedure: Pediatric cardiac surgery
conventional priming
Active Comparator group
Description:
conventional cardiopulmonary priming in young children subjected to cardiac surgery for congenital heart defects with left to right shunt associated with volume or pressure overload.
Treatment:
Procedure: Pediatric cardiac surgery

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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