Clinical Study On Acute Radiotherapy-Induced Oral Mucositis In Patients With Locally Advanced Head And Neck Tumors

Sponsor
Affiliated Cancer Hospital & Institute of Guangzhou Medical University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05364918
Collaborator
(none)
100
1
2
24
4.2

Study Details

Study Description

Brief Summary

To explore a more efficient and scientific clinical treatment plan for acute radiotherapy-induced oral mucositis(RIOM/RTOM).it is hoped that the drug combination can more effectively improve the cure rate of acute RIOM,reduce the degree of oral mucosal injury and utilization rate of analgesic drugs,and reduce the occurrence of severe acute RIOM. Almost all patients with head and neck will have RIOM because of receiving radiation therapy.Studies have shown that the incidence of severe acute RIOM accounted for about 34% to 56%.There is no specific drug when acute RIOM is often accompanied by varying degrees of pain and infection in the mouth.Severe RIOM seriously affects ingestion through the mouth and doesn't conducive to the treatment and prognosis of tumor diseases. To further explore the efficiency and advantages of the combined application of Jeksung and anti-radiation spray in the treatment of acute RIOM at all levels,and provide more data support for relevant clinical treatment.Explore whether the Jeksung with combination of anti-radiation spray can effectively delay the occurrence of acute RIOM and delay the course of the disease.It will be expected to improve the quality of life of cancer patients ,reduce the occurrence of adverse events due during radiotherapy.

Condition or Disease Intervention/Treatment Phase
  • Drug: Jeksung combined with anti-radiation spray
Phase 3

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Clinical Effect Of Application Of Jeksung Combined With Anti-radiation Spray In Patients Radiotherapy-Induced Oral Mucositis Of Local Advanced Head And Neck Tumors
Actual Study Start Date :
Apr 1, 2021
Anticipated Primary Completion Date :
Mar 31, 2023
Anticipated Study Completion Date :
Mar 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Jeksung

Drug: Jeksung combined with anti-radiation spray
Treat radiation stomatitis with Jeksung combined with anti-radiation spray

No Intervention: Control

Outcome Measures

Primary Outcome Measures

  1. Acute radiotherapy-induced oral mucositis [The first day of radiation therapy for head and neck tumors to the last day]

    Occur rate of severe radiotherapy-induced oral mucositis

Secondary Outcome Measures

  1. Oral pain [The first day to the last day of radiation therapy for head and neck tumors]

    Utilization rate of analgesic drugs

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Head and neck cancer was confirmed by patholog

  • Received radical radiotherapy, and were observed and treated by RTOM in the stomatology department

  • Age range: 18-75 years old

  • The estimated survival period is more than 6 months, and the card functional status score (KPS) is 70

  • There are no diseases that affect the treatment of oral mucositis, such as mouth opening restriction, Sjogren's syndrome, etc.

  • Sign the informed consent form

Exclusion Criteria:
  • Failed to complete radiotherapy, or delayed radiotherapy more than 2 weeks than planned

  • There are previous oral mucosal diseases, such as oral lichen planus and pemphigus, which are not effectively controlled or still need long-term drug treatment

  • There are other diseases that affect radiotherapy, such as severe organ function injury, chronic infectious diseases, etc.

  • Had received radiotherapy for head and neck for other diseases;

  • The expected survival time is less than 6 months;

  • Refuse to provide personal information or sign informed consent

  • The investigator judged other conditions that might affect the conduct of the clinical study and the determination of the study results.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Yu Zeng Guangzhou Guangdong China 510000

Sponsors and Collaborators

  • Affiliated Cancer Hospital & Institute of Guangzhou Medical University

Investigators

  • Principal Investigator: Yu Zeng, Dr., Affiliated Cancer Hospital & Institute of Guangzhou Medical University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Affiliated Cancer Hospital & Institute of Guangzhou Medical University
ClinicalTrials.gov Identifier:
NCT05364918
Other Study ID Numbers:
  • Radioactive Oral Mucositis
First Posted:
May 6, 2022
Last Update Posted:
May 6, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 6, 2022