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NCT Number: NCT05441813

Coconut Oil to Prevent Mouth Sores in Pediatric Patients Receiving High Dose Chemotherapy

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.

Recruiting

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Key information

Age range

7 year–26 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

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

About this study

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

Who can participate

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:

  • Written informed consent, HIPAA authorization for release of personal health information, and assent, when applicable from the subject, parent, or legal guardian.
  • Age greater than or equal to 7 years to 26 years at the time of consent
  • Patients planning to undergo myeloablative conditioning regimens in preparation for HSCT
  • ECOG Performance Status of less than or equal to 2 or Lansky/Karnofsky Performance Status of greater than or equal to 50 within 7 days prior to date of enrollment.
  • No evidence of mouth lesions at time of enrollment
  • Ability of the subject and parent/caregiver to understand and comply with study procedures for the entire length of the study
  • Able and willing to swish/spit the oral formulation

Exclusion criteria

Subjects meeting any of the criteria below may not participate in the study:

  • Allergy to tree nuts
  • Planned discharge home prior to engraftment
  • Using coconut oil mouth rinses within 30 days prior to enrollment
  • Using additional mouthcare regimens, other than those allowed in the institutional SOP, prior to admission with a plan to continue use during admission
  • Patient has undergone HSCT within the last 90 days prior to admission

Treatment and study plan

Virgin Coconut Oil

Drug

Standard of care with the addition of virgin coconut oil mouth rinse

Primary outcomes

  1. Severity of Mucositis

    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.

Secondary outcomes

  1. Average Daily Caloric Intake

    Time frame: Day 45

    Oral intake will be calculated quantitatively for each subject during the on-treatment period.

  2. Total Parenteral Nutrition (TPN)

    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.

  3. Opioid Use

    Time frame: Day 45

    Daily opioid use will be calculated quantitatively for each subject in terms of their average Morphine Equivalent Daily Dose (MEDD)

  4. Time to CTCAE Mucositis Grade > 2

    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.

  5. Daily Incidence of Optional Mouth Rinses

    Time frame: Day 45

    Proportion of days during the on-treatment period that optional oral rinse was used.

  6. Incidence and type of oral viral infections

    Time frame: Day 45

    Incidence and type of oral viral infections

  7. Length of Hospitalization

    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.

  8. Days to Absolute Neutrophil Count (ANC) Engraftment

    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

Other outcomes

  1. Oral Rinse Utilization

    Time frame: Day 45

    Reported as a percent of utilization

Study contacts

Contact information is provided by the study sponsor or research team.

Marithza Amaya

CONTACT

[email protected]

980-442-0530

Sceria Jenkins, RN

CONTACT

[email protected]

980-442-2323

Sponsors and collaborators

Lead sponsor

Wake Forest University Health Sciences

Other

Registry information

Official study title

A Randomized, Open-label Study of Coconut Oil Mouth Rinse for Prophylaxis of Severe Oral Mucositis in Pediatric Patients Receiving Myeloablative Conditioning Regimens

Important dates

Study start
2023
Primary completion
2036
Study completion
2036
First posted
Jul 1, 2022
Registry last updated
Jul 22, 2026

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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