ConductScience.org, home

Trial · NCT00231868

A Study of Radiation Therapy and Paclitaxel and Carboplatin in Patients With Uterine Papillary Serous Carcinoma

NCT00231868, Phase 2, Completed, Montefiore Medical Center; results first posted 2020-08-12

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. A Study of Radiation Therapy and Paclitaxel and Carboplatin in Patients With Uterine Papillary Serous Carcinoma. Trials, record NCT00231868. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00231868

On this page

Trial

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

Title
A Study of Radiation Therapy and Paclitaxel and Carboplatin in Patients With Uterine Papillary Serous Carcinoma
NCT number
NCT00231868
Status
Completed
Phases
Phase 2
Enrollment
81 participants, actual
Lead sponsor
Montefiore Medical Center
Conditions
Uterine Cancer
Interventions
Carboplatin and Paclitaxel and Pelvic Radiation Therapy, Carboplatin and Paclitaxel and Pelvic Radiation Therapy, Carboplatin and Paclitaxel and Radiation Therapy
First posted
2005-10-04
Last updated
2020-08-12
Results first posted
2020-08-12
Limitations and caveats
There are minor differences in the carboplatin doses between the current trial and our pilot study.~This is a single institution trial. A limited number of advanced stage patients was accrued.

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryTo Evaluate the Toxicity and Tolerability of Pelvic Radiation "Sandwiched" Between Cycles of Paclitaxel/Carboplatin Chemotherapy in Patients With UPSCUp to 7 years
Overall survival analysis of early stage (stage 1 \& 2) and late stage (stage 3 \& 4)UPSC patients who were prescribed radiation "sanwhiched" between three cycles of paclitaxel/platinum chemotherapy before and after RT. Outcome measures were Progression Free Survival (PFS) and Overall Survival (OS).

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYTo Evaluate the Toxicity and Tolerability of Pelvic Radiation Sandwiched Between Cycles of Paclitaxel/Carboplatin Chemotherapy in Patients With UPSCUp to 7 yearsKaplan-Meier survival analysis of Progression Free Survival (PFS) and Overall Survival (OS).monthsMEAN

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
To Evaluate the Toxicity and Tolerability of Pelvic Radiation Sandwiched Between Cycles of Paclitaxel/Carboplatin Chemotherapy in Patients With UPSCDrug:Carboplatin, Paclitaxel & RadiationEarly stage (PFS)65.5Standard Error 3.6months
To Evaluate the Toxicity and Tolerability of Pelvic Radiation Sandwiched Between Cycles of Paclitaxel/Carboplatin Chemotherapy in Patients With UPSCDrug:Carboplatin, Paclitaxel & RadiationLate stage (PFS)25.8Standard Error 3.0months
To Evaluate the Toxicity and Tolerability of Pelvic Radiation Sandwiched Between Cycles of Paclitaxel/Carboplatin Chemotherapy in Patients With UPSCDrug:Carboplatin, Paclitaxel & RadiationEarly stage (OS)76.5Standard Error 4.3months
To Evaluate the Toxicity and Tolerability of Pelvic Radiation Sandwiched Between Cycles of Paclitaxel/Carboplatin Chemotherapy in Patients With UPSCDrug:Carboplatin, Paclitaxel & RadiationLate stage (OS)35.9Standard Error 5.3months

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDCarboplatin & Paclitaxel & Radiation: Pelvic Radiation Therapy81
Overall StudyCOMPLETEDCarboplatin & Paclitaxel & Radiation: Pelvic Radiation Therapy65
Overall StudyNOT COMPLETEDCarboplatin & Paclitaxel & Radiation: Pelvic Radiation Therapy16

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 totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityCarboplatin & Paclitaxel & Radiation: Pelvic Radiation Therapy1672
Total, other adverse eventsCarboplatin & Paclitaxel & Radiation: Pelvic Radiation Therapy072
Total, serious adverse eventsCarboplatin & Paclitaxel & Radiation: Pelvic Radiation Therapy072

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
22035806RESULT

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 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/NCT00231868

GET https://conductscience.org/api/trials/v1/NCT00231868/registered