RecruitingPhase 4NCT07536152

Antihistamine for Prevention of HTR After Blood Primed CPB

Prophylactic Antihistamine for Prevention of Hypotensive Transfusion Reaction After Blood Primed Cardiopulmonary Bypass in Pediatric Cardiac Surgery: a Randomized-controlled Study


Sponsor

Kasr El Aini Hospital

Enrollment

40 participants

Start Date

Mar 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This study will be a randomized, double-blinded, placebo-controlled study conducted at a university hospital. Forty children undergoing elective repair of a congenital heart defect will be included. The patients will be randomly allocated (20 patients per group) to receive a single intravenous dose of combined chlorpheniramine or normal saline immediately after separation from CPB, before protamine administration.


Eligibility

Min Age: 1 YearMax Age: 7 Years

Inclusion Criteria3

  • Acyanotic congenital heart disease.
  • Age :1 -7 years.
  • Genre: both.

Exclusion Criteria4

  • Redo patient.
  • History of allergy to antihistamines.
  • Bleeding disorders with INR > 1.5 and/or platelets < 50,000.
  • Emergency procedure.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGAntihestamine

chlorpheniramine 0.25 mg/Kg in 2 ml immediately after separation from CPB, before protamine administration

DRUGPlacebo

equal volume normal saline


Locations(1)

Misr Universty for Scince and Technology

Giza, October, Egypt

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07536152


Related Trials