A Randomized Controlled Study on the Improvement of Medical Experience for Patients With Radiation-induced Oropharyngeal Mucositis Based on the RIS System of the Internet of Things

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorNanfang Hospital, Southern Medical University

About this trial

This study is a researcher-initiated, multi-center, prospective, two-arm interventional randomized controlled study across the country. It aims to explore whether an Internet of Things-based RIS system can enhance the medical experience of patients with radiation-induced oropharyngeal mucositis during the diagnosis and treatment process among head and neck cancer patients undergoing radiotherapy.

Eligibility criteria

Qualifiers

Voluntarily sign the informed consent form;

Reached the age of 18 on the date of signing the informed consent form, and under the age of 65;

Patients diagnosed with head and neck tumors and receiving radiotherapy as per the 2017 WHO standards and guidelines.

According to the doctor's assessment, patients may experience radiation-induced oropharyngeal mucositis during radiotherapy.

Disqualifiers

Have other uncontrolled serious diseases, such as unstable heart diseases requiring treatment, poorly controlled diabetes (fasting blood sugar > 1.5 times the upper limit of the normal value), mental disorders, and a severe history of allergies.

Trial design

Treatments tested in this trial

  • RIS system

Treatment groups

110 Participants
are divided into 2 treatment groups