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Trial · NCT05082909

Addition of Probenecid to Penicillin-V Therapy

NCT05082909, Phase 1, Phase 2, Completed, Imperial College London; results first posted 2025-01-30

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Addition of Probenecid to Penicillin-V Therapy. Trials, record NCT05082909. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05082909

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Trial

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

Title
Addition of Probenecid to Penicillin-V Therapy
NCT number
NCT05082909
Status
Completed
Phases
Phase 1, Phase 2
Enrollment
21 participants, actual
Lead sponsor
Imperial College London
Conditions
Infection, Bacterial
Interventions
Probenecid
First posted
2021-10-19
Last updated
2025-01-30
Results first posted
2025-01-30

Source ClinicalTrials.gov

Registered outcomes4

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

ListOutcomeTime frameDescription
PrimaryMeasurement of Total and Unbound Penicillin-V Concentration45 minutes post an observed dose.Measurement of blood concentration at 45 minutes post dose with and without probenecid.
PrimaryMeasurement of Total and Unbound Penicillin-V Concentration180 minutes post an observed dose.Measurement of blood concentration at 180 minutes post dose with and without probenecid.
SecondaryMeasurement of Total and Unbound Probenecid Concentration45 minutes post an observed dose.Measurement of blood concentration at 45 minutes post observed probenecid dose. Combined data for all participants given that the same dose of probenecid was taken by all participants.
SecondaryMeasurement of Total and Unbound Probenecid Concentration180 minutes post an observed dose.Measurement of blood concentration at 180 minutes post observed probenecid dose. Combined data for all participants given that the same dose of probenecid was taken by all participants.

Outcomes4

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMeasurement of Total and Unbound Penicillin-V Concentration45 minutes post an observed dose.mg/LMEAN
PRIMARYMeasurement of Total and Unbound Penicillin-V Concentration180 minutes post an observed dose.mg/LMEAN
SECONDARYMeasurement of Total and Unbound Probenecid Concentration45 minutes post an observed dose.All 20 participants received the same dose (500mg QDS) of probenecid regardless of study arm. Results are therefore presented for all participants for this outcome.mg/LMEAN
SECONDARYMeasurement of Total and Unbound Probenecid Concentration180 minutes post an observed dose.All 20 participants received the same dose (500mg QDS) of probenecid regardless of study arm. Results are therefore presented for all participants for this outcome.mg/LMEAN

Results by group52

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

OutcomeGroupCategoryValueSpreadUnits
Measurement of Total and Unbound Penicillin-V Concentration250mg Penicillin Arm 1Total penicillin concentration (mg/L) - penicillin alone2.07Standard Deviation 0.16mg/L
Measurement of Total and Unbound Penicillin-V Concentration250mg Penicillin Arm 2Total penicillin concentration (mg/L) - penicillin alone2.8Standard Deviation 0.10mg/L
Measurement of Total and Unbound Penicillin-V Concentration500mg Penicillin Arm 1Total penicillin concentration (mg/L) - penicillin alone5.03Standard Deviation 1.46mg/L
Measurement of Total and Unbound Penicillin-V Concentration500mg Penicillin Arm 2Total penicillin concentration (mg/L) - penicillin alone3.62Standard Deviation 1.56mg/L
Measurement of Total and Unbound Penicillin-V Concentration750mg Penicillin Arm 1Total penicillin concentration (mg/L) - penicillin alone6.53Standard Deviation 5.38mg/L
Measurement of Total and Unbound Penicillin-V Concentration750mg Penicillin Arm 2Total penicillin concentration (mg/L) - penicillin alone6.2Standard Deviation 0.8mg/L
Measurement of Total and Unbound Penicillin-V Concentration250mg Penicillin Arm 1Unbound penicillin concentration (mg/L) - penicillin alone0.39Standard Deviation 0.04mg/L
Measurement of Total and Unbound Penicillin-V Concentration250mg Penicillin Arm 2Unbound penicillin concentration (mg/L) - penicillin alone0.56Standard Deviation 0.01mg/L
Measurement of Total and Unbound Penicillin-V Concentration500mg Penicillin Arm 1Unbound penicillin concentration (mg/L) - penicillin alone0.97Standard Deviation 0.22mg/L
Measurement of Total and Unbound Penicillin-V Concentration500mg Penicillin Arm 2Unbound penicillin concentration (mg/L) - penicillin alone0.65Standard Deviation 0.27mg/L

Participant flow18

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPenicillin 250mg QDS THEN Penicillin 250mg QDS Plus Probenecid 500mg QDS3
Overall StudySTARTEDPenicillin 500mg QDS THEN Penicillin 500mg QDS Plus Probenecid 500mg QDS4
Overall StudySTARTEDPenicillin 750mg QDS THEN Penicillin 750mg QDS Plus Probenecid 500mg QDS4
Overall StudySTARTEDPenicillin 250mg QDS Plus Probenecid 500mg QDS THEN Penicillin 250mg QDS.2
Overall StudySTARTEDPenicillin 500mg QDS Plus Probenecid 500mg QDS THEN Penicillin 500mg QDS.6
Overall StudySTARTEDPenicillin 750mg QDS Plus Probenecid 500mg QDS THEN Penicillin 750mg QDS.2
Overall StudyCOMPLETEDPenicillin 250mg QDS THEN Penicillin 250mg QDS Plus Probenecid 500mg QDS3
Overall StudyCOMPLETEDPenicillin 500mg QDS THEN Penicillin 500mg QDS Plus Probenecid 500mg QDS4
Overall StudyCOMPLETEDPenicillin 750mg QDS THEN Penicillin 750mg QDS Plus Probenecid 500mg QDS3
Overall StudyCOMPLETEDPenicillin 250mg QDS Plus Probenecid 500mg QDS THEN Penicillin 250mg QDS.2

Adverse events10

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherMild, expected (GI side effects)Gastrointestinal disordersPenicillin Alone3204
otherMild, expected (GI side effects)Gastrointestinal disordersPenicillin Plus Probenecid5207
otherMild, expected (headache)Nervous system disordersPenicillin Alone1201
otherMild, expected (headache)Nervous system disordersPenicillin Plus Probenecid3203
otherUnexpected, not related to IMPInfections and infestationsPenicillin Alone1201
otherUnexpected, not related to IMPInfections and infestationsPenicillin Plus Probenecid0200
otherUnexpected, not related to IMPMusculoskeletal and connective tissue disordersPenicillin Alone1201
otherUnexpected, not related to IMPMusculoskeletal and connective tissue disordersPenicillin Plus Probenecid0200
otherUnexpected, possible association with IMPMetabolism and nutrition disordersPenicillin Alone1201
otherUnexpected, possible association with IMPMetabolism and nutrition disordersPenicillin Plus Probenecid0200

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPenicillin Alone020
Total, all-cause mortalityPenicillin Plus Probenecid020
Total, other adverse eventsPenicillin Alone720
Total, other adverse eventsPenicillin Plus Probenecid820
Total, serious adverse eventsPenicillin Alone020
Total, serious adverse eventsPenicillin Plus Probenecid020

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 comparisons2

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

ComparisonSource
Penicillin Alone vs Penicillin Plus Probenecid: deaths from any causeTrial comparisons
Penicillin Alone vs Penicillin Plus Probenecid: 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/NCT05082909

GET https://conductscience.org/api/trials/v1/NCT05082909/results?page=2