Viewing Study NCT06525402



Ignite Creation Date: 2024-10-26 @ 3:36 PM
Last Modification Date: 2024-10-26 @ 3:36 PM
Study NCT ID: NCT06525402
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-03-29

Brief Title: Effect of Sodium Bicarbonate Saline and Black Mulberry Syrup on Degree of Oral Mucositis in Children Receiving Chemotherapy
Sponsor: None
Organization: None

Study Overview

Official Title: The Effect of Sodium Bicarbonate Saline and Black Mulberry Syrup on The Degree of Oral Mucositis in Children Receiving Chemotherapy A Randomized Controlled Trial
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-07
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: This study was planned as a randomized controlled experimental study in order to compare the effects of oral care with saline and black mulberry syrup in addition to sodium bicarbonate on oral mucositis level in children aged 6-18 years receiving chemotherapy
Detailed Description: Oral mucositis also known as stomatitis is the most common complication of cancer treatment Mucositis affects the patients nutrition daily functions and quality of life may compromise the ability to tolerate scheduled therapy For this reason the children to be included in the study will be randomly divided into three groups Sodium bicarbonate which is the routine care in the clinic will be administered to the control group and to the intervention groups saline in addition to the routine care and black mulberry syrup will be applied in addition to the routine care Data will be collected according to Patient Information Form International Child Mucositis Assessment Scale ChIMES World Health Organization Mucositis Classification and neutrophil counts Oral care will be applied to the groups 4 times a day for 14 days The International Child Mucositis Rating Scale ChIMES World Health Organization Mucositis Classification and neutrophil counts will be evaluated by the researchers on the 1st 2nd 4th 8th and 16th days

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