Trial · NCT07348510
Diuretic Effect of Aminophylline and Furosemide in Adult Patients Undergoing Cardiac Surgical Procedures
NCT07348510, Not applicable, Recruiting, Cairo University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Diuretic Effect of Aminophylline and Furosemide in Adult Patients Undergoing Cardiac Surgical Procedures. Trials, record NCT07348510. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07348510
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Diuretic Effect of Aminophylline and Furosemide in Adult Patients Undergoing Cardiac Surgical Procedures
- NCT number
- NCT07348510
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 106 participants, estimated
- Lead sponsor
- Cairo University
- Conditions
- Diuretic Effect, Aminophylline, Furosemide, Cardiac Surgical Procedures
- Interventions
- Aminophylline, Furosemide
- First posted
- 2026-01-16
- Last updated
- 2026-01-21
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Measurement of urine output | Two hours after cardiopulmonary bypass | Urine output will be measured at two hours after cardiopulmonary bypass. |
| Secondary | Measurement of urine output at completion of cardiopulmonary bypass | 48 hours after cardiopulmonary bypass | Urine output at completion of cardiopulmonary bypass (CPB) will be measured at 8 hours and 48 hours after CPB. |
| Secondary | Urea level | 48 hours after cardiopulmonary bypass | Urea level will be measured at 8 hours and 48 hours after cardiopulmonary bypass. |
| Secondary | Creatinine level | 48 hours after cardiopulmonary bypass | Creatinine level will be measured at 8 hours and 48 hours after cardiopulmonary bypass. |
| Secondary | Lactate level | 48 hours after cardiopulmonary bypass | Lactate level will be measured at 8 hours and 48 hours after cardiopulmonary bypass. |
| Secondary | Estimated Glomerular Filtration Rate (eGFR) | 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. |
| Secondary | Measurement of fluid balance | 48 hours after cardiopulmonary bypass | Fluid balance at completion of cardiopulmonary bypass (CPB) will be measured at 8 hours and 48 hours after CPB. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07348510
GET https://conductscience.org/api/trials/v1/NCT07348510/registered