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Trial · NCT02272816

Carboplatin AUC-10 With Early PET Scanning in Metastatic Seminoma

NCT02272816, Phase 2, Completed, Barts & The London NHS Trust; results first posted 2019-01-25

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Carboplatin AUC-10 With Early PET Scanning in Metastatic Seminoma. Trials, record NCT02272816. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02272816

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Trial

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

Title
Carboplatin AUC-10 With Early PET Scanning in Metastatic Seminoma
NCT number
NCT02272816
Status
Completed
Phases
Phase 2
Enrollment
48 participants, actual
Lead sponsor
Barts & The London NHS Trust
Conditions
Metastatic Seminoma
Interventions
Carboplatin AUC-10
First posted
2014-10-23
Last updated
2019-01-25
Other registries' IDs
eudract:2009-009882-33
Results first posted
2019-01-25

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
Primary2 - Year Progression Free Survival2 yearsNumber of participants progression free 2 years after registration.
SecondaryMetabolic Response Rate21 daysNumber of participants achieving i) complete metabolic response (CR) and ii) partial metabolic response (PR) after one cycle of treatment.
SecondaryOverall Survival2 yearsSurvival status at 2 years after registration.

Outcomes3

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARY2 - Year Progression Free Survival2 yearsAll participants who received at least one dose of study treatment.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYMetabolic Response Rate21 daysAll participants who completed one cycle of treatment and underwent PET-CT scan on day 17-21.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYOverall Survival2 yearsAll participants who received at least one dose of study treatment.ParticipantsCOUNT_OF_PARTICIPANTS

Results by group5

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

OutcomeGroupCategoryValueSpreadUnits
2 - Year Progression Free SurvivalCarboplatin AUC-1046Participants
Metabolic Response RateCarboplatin AUC-10CR21Participants
Metabolic Response RateCarboplatin AUC-10PR26Participants
Overall SurvivalCarboplatin AUC-10Alive48Participants
Overall SurvivalCarboplatin AUC-10Deceased0Participants

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDCarboplatin AUC-1048
Overall StudyCOMPLETEDCarboplatin AUC-1047
Overall StudyNOT COMPLETEDCarboplatin AUC-101

Adverse events47

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherHypertensionVascular disordersCarboplatin AUC-101481
otherFatigueGeneral disordersCarboplatin AUC-104448111
otherPainGeneral disordersCarboplatin AUC-106487
otherDepressionPsychiatric disordersCarboplatin AUC-101481
otherInsomniaPsychiatric disordersCarboplatin AUC-103484
otherMood swingsPsychiatric disordersCarboplatin AUC-101481
otherSunburnInjury, poisoning and procedural complicationsCarboplatin AUC-101481
otherNeutrophil count decreasedInvestigationsCarboplatin AUC-10344881
otherPlatelet count decreasedInvestigationsCarboplatin AUC-10284853
otherWeight decreasedInvestigationsCarboplatin AUC-101481

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityCarboplatin AUC-10048
Total, other adverse eventsCarboplatin AUC-104748
Total, serious adverse eventsCarboplatin AUC-101248

Papers10

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
7165009BACKGROUNDPubMed
9164194BACKGROUNDPubMed
9667260BACKGROUNDPubMed
11104556BACKGROUNDPubMed
11252008BACKGROUNDPubMed
11345655BACKGROUNDPubMed
15266338BACKGROUNDPubMed
17242396BACKGROUNDPubMed
17242397BACKGROUNDPubMed
31136925DERIVEDPubMed

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.

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/NCT02272816

GET https://conductscience.org/api/trials/v1/NCT02272816/events?page=2