Viewing Study NCT06618911



Ignite Creation Date: 2024-10-26 @ 3:41 PM
Last Modification Date: 2024-10-26 @ 3:41 PM
Study NCT ID: NCT06618911
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-09-24

Brief Title: Evaluation of the Efficacy of Electroacupuncture in the Treatment of Functional Dyspepsia
Sponsor: None
Organization: None

Study Overview

Official Title: Evaluation of the Efficacy of Electroacupuncture in the Treatment of Functional Dyspepsia a Pilot Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Brief Summary Template for the Study

The goal of this clinical trial is to evaluate whether electroacupuncture can treat functional dyspepsia FD in adult participants aged 18 to 65 years including both males and females who have been diagnosed with functional dyspepsia based on the Rome IV criteria The main questions it aims to answer are

Does 5 Hz electroacupuncture improve symptoms in functional dyspepsia patients
Does 100 Hz electroacupuncture improve symptoms in functional dyspepsia patients
Are there differences in the efficacy between 5 Hz and 100 Hz electroacupuncture in treating functional dyspepsia and its subtypes PDS and EPS

Researchers will compare the effects of 5 Hz electroacupuncture 100 Hz electroacupuncture and sham electroacupuncture to determine which approach provides more significant symptom relief and whether different frequencies have varying impacts on FD subtypes

Participants will

Receive electroacupuncture treatment at specific acupoints such as Liangmen Tianshu Zusanli and Xiajuxu for 30-minute sessions 3 times a week for 4 weeks
Be randomly assigned to one of the following groups 5 Hz electroacupuncture 100 Hz electroacupuncture or sham electroacupuncture control
Have their functional dyspepsia symptoms quality of life and any adverse effects monitored and evaluated throughout the study
Detailed Description: None

Study Oversight

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