Viewing Study NCT06265779



Ignite Creation Date: 2024-05-06 @ 8:08 PM
Last Modification Date: 2024-10-26 @ 3:21 PM
Study NCT ID: NCT06265779
Status: RECRUITING
Last Update Posted: 2024-03-06
First Post: 2024-01-22

Brief Title: Transcranial Direct Current Stimulation Combined With Intermittent Oral to Esophageal Tube on Dysphagia
Sponsor: Zeng Changhao
Organization: Peoples Hospital of Zhengzhou University

Study Overview

Official Title: Therapeutic Effect of Transcranial Direct Current Stimulation Combined With Intermittent Oral to Esophageal Feeding on Swallowing Disorders in Patients With Cerebral Infarction Double Blind Randomized Controlled Study
Status: RECRUITING
Status Verified Date: 2024-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: IOEJLCJ-S
Brief Summary: The study is a double-blind randomized controlled trial lasting for 15 days for each participant Patients with post-stroke dysphagia who receive treatment at the Rehabilitation Department are selected as the study subjects The patients are randomly assigned to either the experimental group or the placebo group All patients receive routine rehabilitation therapy and swallowing rehabilitation training along with enteral nutrition support using Intermittent Oro-esophageal Tube In addition to these interventions patients in the experimental group receive transcranial direct current stimulation while the instruments used for patients in the placebo group only illuminate an indicator light without any actual effect
Detailed Description: Transcranial direct current stimulation is currently very popular The study is a double-blind randomized controlled trial lasting for 15 days for each participant Patients with post-stroke dysphagia who receive treatment at the Rehabilitation Department are selected as the study subjects The patients are randomly assigned to either the experimental group or the placebo group All patients receive routine rehabilitation therapy and swallowing rehabilitation training along with enteral nutrition support using Intermittent Oro-esophageal Tube In addition to these interventions patients in the experimental group receive transcranial direct current stimulation while the instruments used for patients in the placebo group only illuminate an indicator light without any actual effect

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None