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NCT06711315Completed

Oral Mucositis Management in Pediatric Oncology Patients

Oral Mucositis Management Supported by MASCC/ISOO Protocols: A Randomized Controlled Trial in Pediatric Oncology Patients

Source: ClinicalTrials.gov · Last updated 2 Dec 2024

Brief summary (registry, in English)

This study evaluated the impact of an oral mucositis care protocol on the severity of mucositis. The main questions it aims to answer are: -What is the severity of mucositis in parents and children who receive oral mucositis education? The data were collected using a descriptive information form, the Children's International Mucositis Evaluation Scale (ChIMES), and the WHO Oral Mucositis Grading Scale. Standard care was applied to the control group. For the intervention group, an oral care protocol was prepared, and the patients received training. The oral care intervention was applied for 14 days and monitored by the researcher. The patients were monitored for oral mucositis on Days 0, 3, 7, and 14. Those in the intervention group received a calendar for documenting their oral care practices.

Status (registry)
Completed
Study type
Interventional
Enrollment
30 (actual)
First submitted
26 Nov 2024
Start date
1 Jun 2023
Primary completion date
6 Aug 2024
Lead sponsor
Zubeyde Ezgi Ercelik
NCT number
NCT06711315

What you commit to

  • Study type: Interventional
  • Participants enrolled: 30
  • From 1 Jun 2023 to the primary completion date, 6 Aug 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • -Conditions that prevent verbal communication (neurodevelopmental delay, verbal speech difficulties, hearing or hearing problems; oral mucositis).

Who the study is looking for

  • Being between 6 and 18 years,
  • Having received at least 1 course of chemotherapy,
  • Having no visual, auditory, or intellectual problems
  • Speaking and understanding Turkish
  • Being willing to participate in the research.

Age in the registry: 6 weeks to 18 weeks · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Zonguldak Bulent Ecevit University Training and Research Hospital
Coordinator of this site? Confirm its status
ZonguldakTurkey (Türkiye)Unknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.