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Trial · NCT04789330

Norepinephrine vs Phenylephrine During General Anesthesia

NCT04789330, Phase 4, Completed, University of California, San Francisco; results first posted 2025-12-18

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Norepinephrine vs Phenylephrine During General Anesthesia. Trials, record NCT04789330. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04789330

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Trial

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

Title
Norepinephrine vs Phenylephrine During General Anesthesia
NCT number
NCT04789330
Status
Completed
Phases
Phase 4
Enrollment
3,626 participants, actual
Lead sponsor
University of California, San Francisco
Conditions
Anesthesia, Surgery, Hypotension
Interventions
Norepinephrine, Phenylephrine
First posted
2021-03-09
Last updated
2026-09-01
Results first posted
2025-12-18
Limitations and caveats
Pragmatic trial with events recorded throughout the eHR

Source ClinicalTrials.gov

Registered outcomes8

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

ListOutcomeTime frameDescription
PrimaryNumber of Participants With Assigned Vasopressor GivenAnesthesia time, up to 24 hoursFirst line vasopressor administration will be measured as a percent of total eligible participants with assigned vasopressor given during anesthesia time, up to 24 hours
SecondaryNumber of Participants Who Died Within 30 Days After Surgery30 daysDeath within 30 days of surgery.
SecondaryNumber of Participants With Acute Kidney Injury (AKI)7 days
AKI is measured using the Kidney Disease: Improving Global Outcomes (KDIGO) definition based on serum creatinine. Acute kidney injury is defined as an increase in serum creatinine ≥ 0.3 mg/dL within 48 hours, or an increase in serum creatinine ≥ 1.5-fold from baseline within 7 days, or initiation of renal replacement therapy within 7 days.
SecondaryNumber of Participants With Severe Acute Kidney Injury7 days
Severe acute kidney injury is assessed using the KDIGO definition based on serum creatinine or need for Renal Replacement Therapy (RRT). Severe Acute Kidney Injury is defined as an increase in serum creatinine ≥ 2-fold from baseline within 7 days, or initiation of renal replacement therapy within 7 days.
SecondaryHospital Length of StayIn-hospital, up to 30 daysDays between date of surgery and hospital discharge
SecondaryNumber of Participants With Myocardial Injury After Non-cardiac Surgery (MINS)7 daysNumber of participants with post-operative myocardial injury defined as a troponin elevation.
SecondaryAdverse Cardio-renal Events7 daysNumber of patients meeting a combined endpoint of AKI and/or MINS
SecondaryRehospitalization Within 30 Days30 daysPatients discharge and readmitted for more than 24 hours within 30 days after surgery

Outcomes8

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Participants With Assigned Vasopressor GivenAnesthesia time, up to 24 hoursParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants Who Died Within 30 Days After Surgery30 daysParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants With Acute Kidney Injury (AKI)7 daysParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants With Severe Acute Kidney Injury7 daysParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYHospital Length of StayIn-hospital, up to 30 daysdaysMEDIAN
SECONDARYNumber of Participants With Myocardial Injury After Non-cardiac Surgery (MINS)7 daysParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYAdverse Cardio-renal Events7 daysParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYRehospitalization Within 30 Days30 daysParticipantsCOUNT_OF_PARTICIPANTS

Results by group16

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Assigned Vasopressor GivenNorepinephrine1570Participants
Number of Participants With Assigned Vasopressor GivenPhenylephrine1627Participants
Number of Participants Who Died Within 30 Days After SurgeryNorepinephrine20Participants
Number of Participants Who Died Within 30 Days After SurgeryPhenylephrine22Participants
Number of Participants With Acute Kidney Injury (AKI)Norepinephrine140Participants
Number of Participants With Acute Kidney Injury (AKI)Phenylephrine135Participants
Number of Participants With Severe Acute Kidney InjuryNorepinephrine28Participants
Number of Participants With Severe Acute Kidney InjuryPhenylephrine31Participants
Hospital Length of StayNorepinephrine4Inter-Quartile Range 2.1 to 7.0days
Hospital Length of StayPhenylephrine4.1Inter-Quartile Range 2.1 to 7.5days

Participant flow16

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDNorepinephrine1,809
Overall StudySTARTEDPhenylephrine1,817
Overall StudySite 1Norepinephrine845
Overall StudySite 1Phenylephrine815
Overall StudySite 2Norepinephrine302
Overall StudySite 2Phenylephrine310
Overall StudySite 3Norepinephrine110
Overall StudySite 3Phenylephrine128
Overall StudySite 4Norepinephrine261
Overall StudySite 4Phenylephrine289

Adverse events6

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAcute Kidney InjuryRenal and urinary disordersNorepinephrine1401,809140
otherAcute Kidney InjuryRenal and urinary disordersPhenylephrine1351,817135
otherMyocardial injuryCardiac disordersNorepinephrine441,80944
otherMyocardial injuryCardiac disordersPhenylephrine381,81738
seriousmortalityCardiac disordersNorepinephrine201,80920
seriousmortalityCardiac disordersPhenylephrine221,81722

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityNorepinephrine201,809
Total, all-cause mortalityPhenylephrine221,817
Total, other adverse eventsNorepinephrine1681,809
Total, other adverse eventsPhenylephrine1591,817
Total, serious adverse eventsNorepinephrine201,809
Total, serious adverse eventsPhenylephrine221,817

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
36925330RESULTPubMed
38242802DERIVEDPubMed

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 comparisons9

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

ComparisonSource
Norepinephrine vs Phenylephrine: Rehospitalization Within 30 DaysTrial comparisons
Norepinephrine vs Phenylephrine: Number of Participants With Myocardial Injury After Non-cardiac Surgery (MINS)Trial comparisons
Norepinephrine vs Phenylephrine: Number of Participants Who Died Within 30 Days After SurgeryTrial comparisons
Norepinephrine vs Phenylephrine: Number of Participants With Severe Acute Kidney InjuryTrial comparisons
Norepinephrine vs Phenylephrine: Number of Participants With Assigned Vasopressor GivenTrial comparisons
Norepinephrine vs Phenylephrine: Number of Participants With Acute Kidney Injury (AKI)Trial comparisons
Norepinephrine vs Phenylephrine: deaths from any causeTrial comparisons
Norepinephrine vs Phenylephrine: Adverse Cardio-renal EventsTrial comparisons
Norepinephrine vs Phenylephrine: serious adverse eventsTrial comparisons

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/NCT04789330

GET https://conductscience.org/api/trials/v1/NCT04789330/registered