Atrium Health Levine Children's Hospital
Charlotte, North Carolina, 28203, United States
Location status: Recruiting
Location contact
Courtney Huddle, DCN, RDN, CSPCC, LDN
PRINCIPAL_INVESTIGATOR
NCT Number: NCT05441813
The purpose of this study is to learn if virgin coconut oil (VCO) mouth rinse can help prevent oral mucositis. The Study Investigator will compare standard of care mucositis prevention rinses with the VCO mouth rinse added to the standard of care mucositis prevention rinses. The severity of oral mucositis between the 2 groups will be evaluated. Some of the standard of care rinses that can be used to prevent mucositis are normal saline, Benadryl (diphenhydramine), Mylanta, lidocaine, or other combinations.
Interested in participating?
Request Info7 year–26 year
All sexes
Interventional
Phase 2
Charlotte, North Carolina, 28203, United States
Location status: Recruiting
Courtney Huddle, DCN, RDN, CSPCC, LDN
PRINCIPAL_INVESTIGATOR
This is a randomized, open-label study. The target population is patients ≥ 7 years to 26 years at time of consent who are planning to undergo myeloablative conditioning regimens in preparation HSCT. The study will be conducted at Levine Children's Hospital, Levine Children's Cancer and Blood Disorders Clinic and Atrium Health. Subjects will be screened and consented within 28 days prior to admission. The planned treatment period for Arm A (standard of care with the addition of VCO mouth rinses) or Arm B (standard of care) will begin at the start of subject's admission for conditioning, followed by transplant event with day of transplant defined as Day 0 and continue through Day +45 following transplant or hospital discharge, whichever comes first. A Safety Follow Up Visit will occur no sooner than 30 days from last study drug treatment
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Subject must meet all the following applicable inclusion criteria to participate in this study:
Exclusion criteria
Subjects meeting any of the criteria below may not participate in the study:
Standard of care with the addition of virgin coconut oil mouth rinse
Time frame: Day 45
Using Area Under the Curve (AUC) of the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 mucositis oral grading scale. This is a 5-point ordered-categorical scale ranging from 1 (asymptomatic or mild symptoms) to 5 (death). For subjects not experiencing oral mucositis, a severity grade of zero will be assigned.
Time frame: Day 45
Oral intake will be calculated quantitatively for each subject during the on-treatment period.
Time frame: Day 45
TPN or hyperalimentation will be calculated quantitatively for each subject as the proportion of days during the on-treatment period that aggressive nutrition support was utilized.
Time frame: Day 45
Daily opioid use will be calculated quantitatively for each subject in terms of their average Morphine Equivalent Daily Dose (MEDD)
Time frame: Day 45
The duration of time (in days) from the initiation of study treatment until the day of the first occurrence of a CTCAE mucositis grade exceeding 2. The CTCAE mucositis grade is a 5-point ordered-categorical scale ranging from 1 (asymptomatic or mild symptoms) to 5 (death). For subjects who do not report a grade exceeding 2, time to CTCAE mucositis grade >2 will be censored at the date of the last completed CTCAE evaluation.
Time frame: Day 45
Proportion of days during the on-treatment period that optional oral rinse was used.
Time frame: Day 45
Incidence and type of oral viral infections
Time frame: Day 45
Length of stay will be calculated for each subject as the number of days from admission date to discharge date +1.
Time frame: Day 45
Days to engraftment will be calculated for each subject as the number of days from Hematopoietic Stem Cell Transplantation (HSCT) to ANC recovery per Center for International Blood and Marrow Transplantation Research (CIBMTR) definition
Time frame: Day 45
Reported as a percent of utilization
Contact information is provided by the study sponsor or research team.
Marithza Amaya
CONTACT
Sceria Jenkins, RN
CONTACT
Wake Forest University Health Sciences
Other
A Randomized, Open-label Study of Coconut Oil Mouth Rinse for Prophylaxis of Severe Oral Mucositis in Pediatric Patients Receiving Myeloablative Conditioning Regimens
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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