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Recruiting NCT07348510

NCT07348510 Diuretic Effect of Aminophylline and Furosemide in Adult Patients Undergoing Cardiac Surgical Procedures

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Clinical Trial Summary
NCT ID NCT07348510
Status Recruiting
Phase
Sponsor Cairo University
Condition Diuretic Effect
Study Type INTERVENTIONAL
Enrollment 106 participants
Start Date 2026-01-17
Primary Completion 2026-07-26

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
AminophyllineFurosemide

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 106 participants in total. It began in 2026-01-17 with a primary completion date of 2026-07-26.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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

Eligibility Criteria

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.

Contact & Investigator

Central Contact

Ahmed M Hassan, MSc

✉ ahm33hassan@gmail.com

📞 00201033752020

Frequently Asked Questions

Who can join the NCT07348510 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Diuretic Effect. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07348510 currently recruiting?

Yes, NCT07348510 is actively recruiting participants. Contact the research team at ahm33hassan@gmail.com for enrollment information.

Where is the NCT07348510 trial being conducted?

This trial is being conducted at Cairo, Egypt.

Who is sponsoring the NCT07348510 clinical trial?

NCT07348510 is sponsored by Cairo University. The trial plans to enroll 106 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology