ConductScience.org, home

Trial · NCT00176826

T-Cell Depletion and Stem Cell Transplant for Immune Deficiencies and Histiocytic Disorders

NCT00176826, Phase 2, Phase 3, Terminated, Masonic Cancer Center, University of Minnesota; results first posted 2014-04-28

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. T-Cell Depletion and Stem Cell Transplant for Immune Deficiencies and Histiocytic Disorders. Trials, record NCT00176826. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00176826

On this page

Trial

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

Title
T-Cell Depletion and Stem Cell Transplant for Immune Deficiencies and Histiocytic Disorders
NCT number
NCT00176826
Status
Terminated
Phases
Phase 2, Phase 3
Enrollment
22 participants, actual
Lead sponsor
Masonic Cancer Center, University of Minnesota
Conditions
Hemophagocytic Lymphohistiocytosis, X-Linked Lymphoproliferative Disorders, Chediak-Higashi Syndrome, Griscelli Syndrome, Immunologic Diseases, Langerhans-Cell Histiocytosis, Hematologic Diseases
Interventions
Stem Cell Transplant, Myeloablative conditioning regimen
First posted
2005-09-15
Last updated
2018-01-23
Results first posted
2014-04-28

Source ClinicalTrials.gov

Registered outcomes7

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

ListOutcomeTime frameDescription
PrimaryTime to Transplant EngraftmentDay 100 Post Transplant
SecondaryNumber of Patients With Treatment Related Mortality.Day 100 Post Transplant
SecondaryNumber of Patients Surviving (Disease-free)1 year
SecondaryNumber of Patients With Grade II-IV Graft-Versus-Host Disease (GVHD)Day 100 Post Transplant
SecondaryNumber of Patients With Graft FailureDay 100 Post transplant
SecondaryNumber of Patients With III-IV Graft-Versus-Host Disease (GVHD)Day 100 Post Transplant
SecondaryNumber of Patients Surviving (Disease-free)3 years

Outcomes7

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYTime to Transplant EngraftmentDay 100 Post TransplantdaysMEAN
SECONDARYNumber of Patients With Treatment Related Mortality.Day 100 Post TransplantparticipantsNUMBER
SECONDARYNumber of Patients Surviving (Disease-free)1 yearparticipantsNUMBER
SECONDARYNumber of Patients With Grade II-IV Graft-Versus-Host Disease (GVHD)Day 100 Post TransplantparticipantsNUMBER
SECONDARYNumber of Patients With Graft FailureDay 100 Post transplantparticipantsNUMBER
SECONDARYNumber of Patients With III-IV Graft-Versus-Host Disease (GVHD)Day 100 Post TransplantparticipantsNUMBER
SECONDARYNumber of Patients Surviving (Disease-free)3 yearsparticipantsNUMBER

Results by group7

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

OutcomeGroupCategoryValueSpreadUnits
Time to Transplant EngraftmentIntent-To-Treat19.8Standard Deviation 5.2days
Number of Patients With Treatment Related Mortality.Intent-To-Treat6participants
Number of Patients Surviving (Disease-free)Intent-To-Treat14participants
Number of Patients With Grade II-IV Graft-Versus-Host Disease (GVHD)Intent-To-Treat4participants
Number of Patients With Graft FailureIntent-To-Treat2participants
Number of Patients With III-IV Graft-Versus-Host Disease (GVHD)Intent-To-Treat1participants
Number of Patients Surviving (Disease-free)Intent-To-Treat10participants

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDIntent-To-Treat22
Overall StudyCOMPLETEDIntent-To-Treat22
Overall StudyNOT COMPLETEDIntent-To-Treat0

Adverse events2

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

TypeEventOrgan systemGroupAffectedAt riskEvents
seriousSecondary MalignancyNeoplasms benign, malignant and unspecified (incl cysts and polyps)Intent-To-Treat1221
seriousDeathGeneral disordersIntent-To-Treat1221

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityIntent-To-Treat
Total, other adverse eventsIntent-To-Treat022
Total, serious adverse eventsIntent-To-Treat222

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/NCT00176826

GET https://conductscience.org/api/trials/v1/NCT00176826/registered