White Tea for Prevention of Chemotherapy Induced Mucositis

Sponsor
Vejle Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04440930
Collaborator
(none)
88
2
2
33.9
44
1.3

Study Details

Study Description

Brief Summary

The aim of this study is to determine the effectiveness of mouthwash with white tea in the prevention of paclitaxel induced oral mucositis in women with breast cancer.

Condition or Disease Intervention/Treatment Phase
  • Other: White tea
  • Other: Salt water with soda
N/A

Detailed Description

Oral mucositis is a common side effect from paclitaxel treatment. It can be very painful and compromise nutrition and oral hygiene, and it may increase the risk of infection. Although oral mucositis is a common side effect to chemotherapy, no available treatment is yet available that can effectively prevent or treat oral mucositis.

Based on the knowledge that white tea has anti-inflammatory, anti-oxidant and anti-microbial effect, the current study aims to assess the effect of mouth wash with white tea on paclitaxel induced oral mucositis in women with breast cancer.

This study is a phase II randomized controlled trial in which eligible patients will be allocated to a control group (CG) and a study group (SG). The CG will use salt water with soda for mouthwash eight to ten times a day and the SG will use white tea for mouthwash five to six times a day.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
88 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Can White Tea Prevent Oral Mucositis in Patients Receiving Neoadjuvant or Adjuvant Treatment With Paclitaxel for Breast Cancer? A Randomized Trial
Actual Study Start Date :
Sep 2, 2020
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Jul 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: White tea

Other: White tea
Mouthwash with white tea five to six times a day for nine weeks

Active Comparator: Salt water with soda

Other: Salt water with soda
Mouthwash with salt water and soda eight to ten times a day for nine weeks

Outcome Measures

Primary Outcome Measures

  1. Incidence of oral mucositis grade 2 or higher as measured by the Revised Oral Assessment Guide. [up to nine weeks]

    Nine categories are included in the Revised Oral Assessment Guide tool: voice, lips, mucous, tongue, gums, teeth, saliva, denture and swallowing. Each category is described and rated according to a score of 1 (healthy) to 3 (severe problems).

Secondary Outcome Measures

  1. Frequency of daily mouthwashes [once a week over a period of nine weeks]

    Number of daily mouthwashes will be registered

  2. Frequency of daily tooth brushings [once a week over a period of nine weeks]

    Number of daily tooth brushings will be registered

  3. Pain intensity in the oral cavity as measured on the Numeric Rating Scale (NRS). [Once a week over a period of nine weeks]

    Numeric Rating Scale 0-10; 0=no pain, 10=worst possible pain

  4. Date of onset of oral mucositis grade 2 or higher as measured by Revised Oral Assessment Guide. [Once a week until oral mucositis occurs up to nine weeks]

    Nine categories are included in the Revised Oral Assessment Guide tool: voice, lips, mucous, tongue, gums, teeth, saliva, denture and swallowing. Each category is described and rated according to a score of 1 (healthy) to 3 (severe problems).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Woman with breast cancer

  • Planned neoadjuvant or adjuvant paclitaxel treatment

  • Age ≥ 18 years

  • Understand and speak Danish

  • Written and orally informed consent

Exclusion Criteria:
  • Palliative treatment with paclitaxel

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Oncology, Vejle Hospital Vejle Denmark
2 Department of Oncology, Vejle Hospital Vejle Denmark

Sponsors and Collaborators

  • Vejle Hospital

Investigators

  • Study Chair: Erik H Jakobsen, MD, Vejle Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Vejle Hospital
ClinicalTrials.gov Identifier:
NCT04440930
Other Study ID Numbers:
  • WHITE TEA
First Posted:
Jun 22, 2020
Last Update Posted:
Feb 24, 2022
Last Verified:
Feb 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Vejle Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 24, 2022