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NCT Number: NCT07348510

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

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

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cairo University

Cairo, 12613, Egypt

Location status: Recruiting

Location contact

Ahmed M Hassan, MSc

CONTACT

[email protected]

00201033752020

Maged Abdel Waha, MD

SUB_INVESTIGATOR

Maged Salah, MD

SUB_INVESTIGATOR

Pierre Zarif, MD

SUB_INVESTIGATOR

Sherif Mamdouh, MD

SUB_INVESTIGATOR

About this study

Acute Kidney injury (AKI) is a serious and common complication after either adult or pediatric cardiac surgery.

The results of a recent meta-analysis suggested that loop diuretics (furosemide) may reduce postoperative creatinine clearance, whereas aldosterone agonists (spironolactone) increase the incidence of cardiac surgery-associated acute kidney injury (CSA-AKI). Diuretics are not recommended for the prevention of AKI, but loop diuretics may be used for the management of volume overload Aminophylline in cardiac surgery can reduce the frequency of AKI and could be used in the prevention of AKI as a safe and efficient modality in high-risk patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age from 18-65 years.
  • Both sexes.
  • All adult patients presenting for elective cardiac surgical procedures performed on cardiopulmonary bypass (Coronary artery bypass surgery, Cardiac valve repair and/or replacement, Repair of large septal defects, Repair and/or palliation of congenital heart defects, Transplantation, surgery of thoracic aneurysms.).
  • Body mass index (BMI) ranged between 20 and 40 kg/m2.

Exclusion criteria

  • Sensitivity or contraindication to Aminophylline or furosemide
  • Stage-5 chronic kidney disease (CKD) [Glomerular filtration rate (GFR) of less than 15 mL/min].
  • The presence of both factors (GFR less than 60 mL/min and albumin greater than 30 mg per gram of creatinine) along with abnormalities of kidney structure or function for greater than three months signifies chronic kidney disease.
  • 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, etc).
  • Patient refusal.

Treatment and study plan

Aminophylline

Drug

Patients will receive Aminophylline.

Furosemide

Drug

Patients will receive furosemide.

Primary outcomes

  1. Measurement of urine output

    Time frame: Two hours after cardiopulmonary bypass

    Urine output will be measured at two hours after cardiopulmonary bypass.

Secondary outcomes

  1. Measurement of urine output at completion of cardiopulmonary bypass

    Time frame: 48 hours after cardiopulmonary bypass

    Urine output at completion of cardiopulmonary bypass (CPB) will be measured at 8 hours and 48 hours after CPB.

  2. Urea level

    Time frame: 48 hours after cardiopulmonary bypass

    Urea level will be measured at 8 hours and 48 hours after cardiopulmonary bypass.

  3. Creatinine level

    Time frame: 48 hours after cardiopulmonary bypass

    Creatinine level will be measured at 8 hours and 48 hours after cardiopulmonary bypass.

  4. Lactate level

    Time frame: 48 hours after cardiopulmonary bypass

    Lactate level will be measured at 8 hours and 48 hours after cardiopulmonary bypass.

  5. Estimated Glomerular Filtration Rate (eGFR)

    Time frame: 48 hours after cardiopulmonary bypass

    Estimated Glomerular Filtration Rate (eGFR) at completion of cardiopulmonary bypass (CPB) will be measured at 8 hours and 48 hours after CPB.

  6. Measurement of fluid balance

    Time frame: 48 hours after cardiopulmonary bypass

    Fluid balance at completion of cardiopulmonary bypass (CPB) will be measured at 8 hours and 48 hours after CPB.

Study contacts

Contact information is provided by the study sponsor or research team.

Ahmed M Hassan, MSc

CONTACT

[email protected]

00201033752020

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Comparison Between the Diuretic Effect of Aminophylline and Furosemide in Adult Patients Undergoing Cardiac Surgical Procedures: A Randomized Controlled Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jan 16, 2026
Registry last updated
Jan 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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