CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 31 enrolled
Drug / intervention
tDCSdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01863017
NCT01863017N/ACompleted
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Pilot Study of Startle-response Test to Assess Transcranial Direct Current Stimulation- Induced Modulation of Hyperphagia in Prader-Willi Syndrome

University of Kansas Medical Center·interventional·Posted May 27, 2013·Updated Apr 26, 2019

In Brief

A clinical study evaluating tDCS for Hyperphagia and Prader-Willi Syndrome. Completed, enrolled 31 participants across 3 sites.

Detailed Summary

The purpose of this study is to determine the effects of transcranial direct current stimulation (tDCS) as it modifies hyperphagia in obese subjects, non-obese subjects, and subjects with Prader-Willi syndrome (PWS).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHyperphagia, Prader-Willi Syndrome
CountriesUnited States
CollaboratorsPrader-Willi Syndrome Association USA, Harvard Medical School (HMS and HSDM), Foundation for Prader-Willi Research

Timeline

N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedMay 27, 2013
Enrollment StartApr 1, 2013
Primary CompletionOct 6, 2016
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 13.1 years ago

Interventions

tDCSdevice