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Trial · NCT00595127

Hematopoietic Stem Cell Transplantation for Treatment of Patients With Fanconi Anemia Lacking a Genotypically Identical Donor, Using Total Body Irradiation, Cyclophosphamide and Fludarabine

NCT00595127, Not applicable, Completed, Memorial Sloan Kettering Cancer Center; results first posted 2016-08-10

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Hematopoietic Stem Cell Transplantation for Treatment of Patients With Fanconi Anemia Lacking a Genotypically Identical Donor, Using Total Body Irradiation, Cyclophosphamide and Fludarabine. Trials, record NCT00595127. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00595127

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Trial

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

Title
Hematopoietic Stem Cell Transplantation for Treatment of Patients With Fanconi Anemia Lacking a Genotypically Identical Donor, Using Total Body Irradiation, Cyclophosphamide and Fludarabine
NCT number
NCT00595127
Status
Completed
Phases
Not applicable
Enrollment
21 participants, actual
Lead sponsor
Memorial Sloan Kettering Cancer Center
Conditions
Fanconi Anemia
Interventions
Cyclophosphamide, Fludarabine, Total body irradiation (TBI)
First posted
2008-01-16
Last updated
2016-08-10
Results first posted
2016-08-10

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryIncidence & Quality of Engraftment & Hematopoietic Reconstitution8 yearsNumber of patients who engrafted

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYIncidence & Quality of Engraftment & Hematopoietic Reconstitution8 yearsparticipantsNUMBER

Results by group1

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

OutcomeGroupCategoryValueSpreadUnits
Incidence & Quality of Engraftment & Hematopoietic ReconstitutionCyclophosphamide and Fludarabine19participants

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDCyclophosphamide and Fludarabine21
Overall StudyCOMPLETEDCyclophosphamide and Fludarabine11
Overall StudyNOT COMPLETEDCyclophosphamide and Fludarabine10

Adverse events25

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAlkaline phosphataseMetabolism and nutrition disordersCyclophosphamide and Fludarabine321
otherBilirubinBlood and lymphatic system disordersCyclophosphamide and Fludarabine1021
otherHemoglobin (Hgb)Metabolism and nutrition disordersCyclophosphamide and Fludarabine2121
otherHyperglycemiaMetabolism and nutrition disordersCyclophosphamide and Fludarabine1521
otherHyperkalemiaMetabolism and nutrition disordersCyclophosphamide and Fludarabine421
otherHypermagnesmiaMetabolism and nutrition disordersCyclophosphamide and Fludarabine221
otherHypertriglyceridemiaMetabolism and nutrition disordersCyclophosphamide and Fludarabine221
otherHypocalcemiaMetabolism and nutrition disordersCyclophosphamide and Fludarabine221
otherHypokalemiaMetabolism and nutrition disordersCyclophosphamide and Fludarabine1421
otherHyponatremiaMetabolism and nutrition disordersCyclophosphamide and Fludarabine821

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityCyclophosphamide and Fludarabine
Total, other adverse eventsCyclophosphamide and Fludarabine2121
Total, serious adverse eventsCyclophosphamide and Fludarabine521

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 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/NCT00595127

GET https://conductscience.org/api/trials/v1/NCT00595127/events?page=2