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Trial · NCT07909954

Accelerated Theta-Burst Stimulation for Refractory Central Post-Stroke Pain

NCT07909954, Not applicable, Not yet recruiting, Duke University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Accelerated Theta-Burst Stimulation for Refractory Central Post-Stroke Pain. Trials, record NCT07909954. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07909954

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Trial

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

Title
Accelerated Theta-Burst Stimulation for Refractory Central Post-Stroke Pain
NCT number
NCT07909954
Status
Not yet recruiting
Phases
Not applicable
Enrollment
30 participants, estimated
Lead sponsor
Duke University
Conditions
Central Post-Stroke Pain, Stroke, Ischemic Stroke and Hemorrhagic Stroke
Interventions
High-dose accelerated intermittent theta burst stimulation (aiTBS), Low-dose accelerated intermittent theta burst stimulation (aiTBS)
First posted
2026-11-02
Last updated
2026-11-02

Source ClinicalTrials.gov

Registered outcomes6

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

ListOutcomeTime frameDescription
PrimaryFeasibility, as measured by the proportion of participants who can complete 80% of stimulation sessionsFrom the time of stimulation (day 1) until end of stimulation (day 5)
PrimaryFeasibility, as measured by proportion of participants who complete 80% of stimulation daysFrom the time of stimulation (day 1) until end of stimulation (day 5)
PrimaryFeasibility, as measured by consent rate of those screenedBaseline
PrimarySafety, as measured by the number of adverse eventsDay 90
PrimaryPain as measured by Visual Analog Scale (VAS)Baseline, 7 days, and 90 daysThe VAS consists of a scale from 0 ("no pain") to 10 ("worst possible pain").
SecondaryThalamo-cortical disconnection index (TCDI), derived from MRIBaselineMeasuring thalamo-cortical disconnection index (TCDI) as a potential biomarker to predict treatment response.

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/NCT07909954

GET https://conductscience.org/api/trials/v1/NCT07909954/registered