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Trial · NCT00743106

The Effect of Fenoldopam in Solitary Partial Nephrectomy Surgery

NCT00743106, Not applicable, Terminated, The Cleveland Clinic; results first posted 2016-10-31

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. The Effect of Fenoldopam in Solitary Partial Nephrectomy Surgery. Trials, record NCT00743106. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00743106

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
The Effect of Fenoldopam in Solitary Partial Nephrectomy Surgery
NCT number
NCT00743106
Status
Terminated
Phases
Not applicable
Enrollment
90 participants, actual
Lead sponsor
The Cleveland Clinic
Conditions
Partial Nephrectomy
Interventions
Fenoldopam, Placebo
First posted
2008-08-28
Last updated
2018-09-19
Results first posted
2016-10-31

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryGlomerular Filtration Rate (GFR) Percentage of Change From Baselinepercentage of change from baseline to post-operatively day 3
Our intended primary analysis was to assess the effect of fenoldopam vs placebo on the GFR at post-operative day (POD) 3 with an analysis of covariance adjusting for the baseline GFR. However, because the intervention-by-baseline GFR interaction using GFR at POD 3 as the outcome was significant (P ¼ .006), the analysis of covariance was not valid. We, therefore, used the GFR percentage of change from baseline to POD 3 as the primary outcome.
SecondaryPostoperative Creatinine (mg/dL)"immediately postoperative, postoperative day 1, postoperative day 2, postoperative day 3, postoperative day 4"assessed the effect of fenoldopam on creatinine over time (immediately postoperatively and on postoperative day 1, 2, 3, 4)

Outcomes2

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYGlomerular Filtration Rate (GFR) Percentage of Change From Baselinepercentage of change from baseline to post-operatively day 3percentage changeMEAN
SECONDARYPostoperative Creatinine (mg/dL)immediately postoperative, postoperative day 1, postoperative day 2, postoperative day 3, postoperative day 4mg/dLMEAN

Results by group12

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Glomerular Filtration Rate (GFR) Percentage of Change From BaselinePlacebo-39Standard Deviation 28percentage change
Glomerular Filtration Rate (GFR) Percentage of Change From BaselineFenoldopam-28Standard Deviation 38percentage change
Postoperative Creatinine (mg/dL)Placeboimmediately postoperative1.44Standard Error 0.07mg/dL
Postoperative Creatinine (mg/dL)Fenoldopamimmediately postoperative1.37Standard Error 0.06mg/dL
Postoperative Creatinine (mg/dL)Placebopostoperative day 12.14Standard Error 0.11mg/dL
Postoperative Creatinine (mg/dL)Fenoldopampostoperative day 12.04Standard Error 0.12mg/dL
Postoperative Creatinine (mg/dL)Placebopostoperative day 22.66Standard Error 0.23mg/dL
Postoperative Creatinine (mg/dL)Fenoldopampostoperative day 22.38Standard Error 0.19mg/dL
Postoperative Creatinine (mg/dL)Placebopostoperative day 32.65Standard Error 0.25mg/dL
Postoperative Creatinine (mg/dL)Fenoldopampostoperative day 32.46Standard Error 0.25mg/dL

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPlacebo42
Overall StudySTARTEDFenoldopam48
Overall StudyCOMPLETEDPlacebo34
Overall StudyCOMPLETEDFenoldopam43
Overall StudyNOT COMPLETEDPlacebo8
Overall StudyNOT COMPLETEDFenoldopam5

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 totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPlacebo
Total, all-cause mortalityFenoldopam
Total, other adverse eventsPlacebo034
Total, other adverse eventsFenoldopam042
Total, serious adverse eventsPlacebo034
Total, serious adverse eventsFenoldopam042

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
39607014DERIVED

Source PubMed

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 comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
Fenoldopam vs Placebo: serious adverse events

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT00743106

GET https://conductscience.org/api/trials/v1/NCT00743106/registered