Viewing Study NCT06472024



Ignite Creation Date: 2024-07-17 @ 11:47 AM
Last Modification Date: 2024-10-26 @ 3:32 PM
Study NCT ID: NCT06472024
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-06-26
First Post: 2024-06-13

Brief Title: Assessing Manual Acupunctures Impact on Mucositis From Nasopharynx Cancer Radiotherapy A Visual Analogue Scale VAS and Quality of Life Study
Sponsor: Indonesia University
Organization: Indonesia University

Study Overview

Official Title: Effects Of Manual Acupuncture On Mucositis Due To Radiotherapy For Nasopharynx Cancer On Visual Analogue Scale Vas Score And Quality Of Life
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-06
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: None
Brief Summary: The goal of this clinical trial is to learn if acupuncture can play a role in reducing pain and improving the quality of life of post-radiotherapy nasopharyngeal cancer mucositis patients The main questions it aims to answer are

- Do manual acupuncture and medication therapy affect pain intensity as measured by the visual analogue scale VAS in patients with oral mucositis compared with sham manual acupuncture and medication

Participants will receive acupuncture therapy 2 times a week for 3 weeks
Detailed Description: This is a clinical trial study to evaluate the role of acupuncture in pain relief and improving the quality of life of nasopharyngeal cancer patients with post-radiotherapy mucositis Participants were 30 menfemales with mucositis in post-radiotherapy nasopharyngeal cancer aged 19-59 years They will be divided into 2 groups 1 verum acupuncture and 2 sham acupuncture Acupuncture is scheduled 2 times per week for 3 weeks Research assessment on pain scale and improvement in quality of life

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