Hyperbaric Oxygen and Its Effect on Radiation Induced Long Term Side Effects

Sponsor
State University of New York - Upstate Medical University (Other)
Overall Status
Completed
CT.gov ID
NCT02450305
Collaborator
(none)
53
1
101.6
0.5

Study Details

Study Description

Brief Summary

The investigators intend to determine if patients that are already undergoing Hyperbaric Oxygen (HBO) therapy one year post treatment with radiation therapy for head and neck cancer, experience improvement in xerostomia and/or taste alteration. The investigators will enroll a similar demographic one year post treatment with radiation therapy that does not receive HBO therapy. This is a quality of life study.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Radiation therapy is a commonly utilized treatment modality for head and neck cancer patients. Xerostomia (i.e. dry mouth) (and taste change) are common and most significant side effects of this treatment. Xerostomia leads to several complications for patients including difficulty in chewing, speaking, swallowing, taste and smell abnormalities, oral infections and inflammation, osteoradionecrosis, dental caries and periodontal disease. These conditions tend to lead to an overall decreased quality of life for patients affected.

    A possible modality for the treatment of xerostomia is the use of hyperbaric oxygen (HBO) therapy. HBO is the medical use of oxygen at a level higher than atmospheric pressure. It has been proposed that HBO results in accelerated blood vessel growth and repair in tissue injuries by increasing the oxygen partial pressure gradient (Bennett, 2005). Today, the use of HBO is widely accepted for both the treatment and prevention of radiation induced toxicities such as osteoradionecrosis and soft tissue necrosis.

    Here at Upstate University Hospital, the investigators treat approximately 20 patients each year with hyperbaric oxygen for either the prevention or management of radiation induced complications such as osteoradionecrosis and /or soft tissue necrosis. The investigators would like to use this group of patients to evaluate the effect of HBO in the improvement of radiation induced xerostomia (and or taste change). The investigators' data will be collected from patients with the use of periodic quality of life questionnaires at 5 timepoints, as well as data relating to the treatment each patient was given. .

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    53 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Hyperbaric Oxygen and Its Effect on Radiation Induced Long Term Side Effects
    Study Start Date :
    Aug 1, 2013
    Actual Primary Completion Date :
    Jan 19, 2022
    Actual Study Completion Date :
    Jan 19, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Treated with HBO

    QOL questionnaires at 5 time points for those having HBO therapy at least one year post radiation therapy for head and neck cancer, daily x6 weeks

    Not treated with HBO

    QOL questionnaires for those at least one year post radiation therapy for head and neck cancer at 5 times points.

    Outcome Measures

    Primary Outcome Measures

    1. Xerostomia [one year]

      The improvement of xerostomia following HBO therapy will be measured using standard RTOG head and neck cancer questionnaires.

    Secondary Outcome Measures

    1. Taste alteration [one year]

      The improvement of taste alteration following HBO therapy will be measured using standard RTOG head and neck cancer questionnaires.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • males and females age > 18 previous radiation therapy to the head and neck region at least one year from end of treatment
    Exclusion Criteria:
    • history of parotidectomy history of dementia

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 SUNY Upstate Medical University Syracuse New York United States 13210

    Sponsors and Collaborators

    • State University of New York - Upstate Medical University

    Investigators

    • Principal Investigator: Marvin Heyboer, MD, State University of New York - Upstate Medical University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Marvin Heyboer, MD, State University of New York - Upstate Medical University
    ClinicalTrials.gov Identifier:
    NCT02450305
    Other Study ID Numbers:
    • 482428 HBO
    First Posted:
    May 21, 2015
    Last Update Posted:
    May 5, 2022
    Last Verified:
    May 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 5, 2022