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Trial · NCT02282514

Stem Cell Transplantation for Stiff Person Syndrome (SPS)

NCT02282514, Phase 1, Phase 2, Terminated, Northwestern University; results first posted 2021-01-06

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Stem Cell Transplantation for Stiff Person Syndrome (SPS). Trials, record NCT02282514. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02282514

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Trial

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

Title
Stem Cell Transplantation for Stiff Person Syndrome (SPS)
NCT number
NCT02282514
Status
Terminated
Phases
Phase 1, Phase 2
Enrollment
23 participants, actual
Lead sponsor
Northwestern University
Conditions
Stiff-Person Syndrome
Interventions
Autologous Hematopoietic Stem Cells, Cyclophosphamide, Mesna, rATG, Methylprednisolone, G-CSF, Rituxan
First posted
2014-11-04
Last updated
2021-01-27
Results first posted
2021-01-06

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
PrimaryOverall SurvivalMean 3.6 yearsNumber of Participants who Did Not Experience Treatment-Related Mortality
SecondaryReduction of Muscle Relaxation Anti-spasmatic MedicationsMean 3.6 yearsDecrease (50%) and complete discontinuation of muscle relaxation anti-spasmatic medications
SecondaryShort-form 36 Quality of Life Questionnaire (SF-36 QOL)mean 3.6 yearsImprovement is defined as a statistically significant change in SF-36 QOL score. The scale is 0-100. The lower the score the worse quality of life.

Outcomes3

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYOverall SurvivalMean 3.6 yearsparticipantsNUMBER
SECONDARYReduction of Muscle Relaxation Anti-spasmatic MedicationsMean 3.6 yearsParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYShort-form 36 Quality of Life Questionnaire (SF-36 QOL)mean 3.6 yearsunits on a scaleGEOMETRIC_MEAN

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
Overall SurvivalHematopoietic Stem Cell Transplantation23participants
Reduction of Muscle Relaxation Anti-spasmatic MedicationsHematopoietic Stem Cell Transplantation14Participants
Short-form 36 Quality of Life Questionnaire (SF-36 QOL)Hematopoietic Stem Cell TransplantationPre Treatment37.75Standard Deviation 12.81units on a scale
Short-form 36 Quality of Life Questionnaire (SF-36 QOL)Hematopoietic Stem Cell TransplantationPost Treatment58.35Standard Deviation 22.81units on a scale

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDHematopoietic Stem Cell Transplantation23
Overall StudyCOMPLETEDHematopoietic Stem Cell Transplantation23
Overall StudyNOT COMPLETEDHematopoietic Stem Cell Transplantation0

Adverse events2

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherHyperglycemiaEndocrine disordersHematopoietic Stem Cell Transplantation5235
seriousNon Treatment Related DeathGeneral disordersHematopoietic Stem Cell Transplantation1231

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityHematopoietic Stem Cell Transplantation123
Total, other adverse eventsHematopoietic Stem Cell Transplantation523
Total, serious adverse eventsHematopoietic Stem Cell Transplantation123

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
33318163RESULT

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/NCT02282514

GET https://conductscience.org/api/trials/v1/NCT02282514/registered