Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07348510

Diuretic Effect of Aminophylline and Furosemide in Adult Patients Undergoing Cardiac Surgical Procedures

Led by Cairo University · Updated on 2026-01-21

106

Participants Needed

1

Research Sites

27 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This work aims to investigate the diuretic effect of Aminophylline in comparison to Furosemide in adult patients undergoing cardiac surgical procedures.

CONDITIONS

Official Title

Diuretic Effect of Aminophylline and Furosemide in Adult Patients Undergoing Cardiac Surgical Procedures

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age from 18-65 years.
  • Both sexes.
  • Adult patients presenting for elective cardiac surgical procedures performed on cardiopulmonary bypass including coronary artery bypass surgery, cardiac valve repair and/or replacement, repair of large septal defects, repair and/or palliation of congenital heart defects, transplantation, and surgery of thoracic aneurysms.
  • Body mass index (BMI) between 20 and 40 kg/m2.
Not Eligible

You will not qualify if you...

  • Sensitivity or contraindication to Aminophylline or Furosemide.
  • Stage-5 chronic kidney disease with glomerular filtration rate (GFR) less than 15 mL/min.
  • Chronic kidney disease defined by GFR less than 60 mL/min and albumin greater than 30 mg per gram of creatinine with kidney structure or function abnormalities for more than three months.
  • Recipients of dialysis before surgery.
  • Recipients of solid-organ transplantation before surgery.
  • Emergency cardiac surgical procedures (e.g., left main coronary artery bypass graft, stuck valves).
  • Patient refusal.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Cairo University

Cairo, Egypt, 12613

Actively Recruiting

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Research Team

A

Ahmed M Hassan, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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