ConductScience.org, home

Trial · NCT00568802

A Pilot Therapeutic Trial Using Hydroxyurea in Type II and Type III Spinal Muscular Atrophy Patients

NCT00568802, Phase 1, Phase 2, Completed, Stanford University; results first posted 2019-10-02

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. A Pilot Therapeutic Trial Using Hydroxyurea in Type II and Type III Spinal Muscular Atrophy Patients. Trials, record NCT00568802. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00568802

On this page

Trial

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

Title
A Pilot Therapeutic Trial Using Hydroxyurea in Type II and Type III Spinal Muscular Atrophy Patients
NCT number
NCT00568802
Status
Completed
Phases
Phase 1, Phase 2
Enrollment
27 participants, actual
Lead sponsor
Stanford University
Conditions
Muscular Atrophy, Spinal
Interventions
Hydroxyurea, Placebo to match hydroxyurea
First posted
2007-12-06
Last updated
2019-10-02
Results first posted
2019-10-02

Source ClinicalTrials.gov

Registered outcomes5

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

ListOutcomeTime frameDescription
PrimaryEfficacy: Functional Motor Testing, Including Gross Motor Function Measure (GMFM) and Timed Motor TestsUp to 6 years, 2 months
PrimarySafety: Frequency of Adverse Events/Lab AbnormalitiesUp to 6 years, 2 months
SecondaryPulmonary Function TestingUp to 6 years, 2 months
SecondaryMotor Unit Number Estimation (MUNE)Up to 6 years, 2 months
SecondaryBiomarker Assays: SMN Protein and SMN mRNAUp to 6 years, 2 months

Outcomes5

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYEfficacy: Functional Motor Testing, Including Gross Motor Function Measure (GMFM) and Timed Motor TestsUp to 6 years, 2 monthsData for this outcome measure are no longer accessible; the PI has left institution and all efforts to locate the data have been exhausted.
PRIMARYSafety: Frequency of Adverse Events/Lab AbnormalitiesUp to 6 years, 2 monthsData for this outcome measure are no longer accessible; the PI has left institution and all efforts to locate the data have been exhausted.
SECONDARYPulmonary Function TestingUp to 6 years, 2 monthsData for this outcome measure are no longer accessible; the PI has left institution and all efforts to locate the data have been exhausted.
SECONDARYMotor Unit Number Estimation (MUNE)Up to 6 years, 2 monthsData for this outcome measure are no longer accessible; the PI has left institution and all efforts to locate the data have been exhausted.
SECONDARYBiomarker Assays: SMN Protein and SMN mRNAUp to 6 years, 2 monthsData for this outcome measure are no longer accessible; the PI has left institution and all efforts to locate the data have been exhausted.

Results by group0

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

None in this release.

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDAll Participants27
Overall StudyCOMPLETEDAll Participants24
Overall StudyNOT COMPLETEDAll Participants3

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 totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityHydroxyurea
Total, all-cause mortalityPlacebo
Total, other adverse eventsHydroxyurea00
Total, other adverse eventsPlacebo00
Total, serious adverse eventsHydroxyurea00
Total, serious adverse eventsPlacebo00

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/NCT00568802

GET https://conductscience.org/api/trials/v1/NCT00568802/registered