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Trial · NCT01623622

Study of HC-58 in Upper Limb Hemiplegic Patients After Stroke

NCT01623622, Phase 2, Completed, Asahi Kasei Therapeutics Corporation

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Study of HC-58 in Upper Limb Hemiplegic Patients After Stroke. Trials, record NCT01623622. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01623622

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Trial

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

Title
Study of HC-58 in Upper Limb Hemiplegic Patients After Stroke
NCT number
NCT01623622
Status
Completed
Phases
Phase 2
Enrollment
270 participants, estimated
Lead sponsor
Asahi Kasei Therapeutics Corporation
Conditions
Severe Upper Limb Hemiplegia
Interventions
HC-58, Placebo
First posted
2012-06-20
Last updated
2017-02-15

Source ClinicalTrials.gov

Registered outcomes10

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

ListOutcomeTime frameDescription
PrimaryOnset of shoulder hand syndrome12 weeksThe incidence rate of shoulder hand syndrome
PrimaryChange from Baseline in the modified Barthel index (MBI) and MBI efficiency12 weeksMBI efficiency means MBI gain divided by period of administration
PrimaryChange from Baseline in the Fugl-Meyer Assessment (FMA) (upper limb) and FMA efficiency12 weeksFMA efficiency means FMA gain divided by period of administration
SecondaryPain score by numeric rating scale12 weeks
SecondarySwelling asymmetry between hands12 weeks
SecondaryDiscolouration of the skin of the hand12 weeks
SecondaryDifference in skin temperature between hands12 weeks
SecondaryDecreased range of motion12 weeks
SecondaryRadiographic finding of bone12 weeks
SecondaryBone metabolic marker12 weeks

Outcomes0

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

None in this release.

Results by group0

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

None in this release.

Participant flow0

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

None in this release.

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 totals0

The totals the trial posted for each group.

None in this release.

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/NCT01623622

GET https://conductscience.org/api/trials/v1/NCT01623622/registered