Evaluation of Post-covid 19 Patients Who Receive Ozonetheraphy With Thorax CT

Sponsor
Gaziosmanpasa Research and Education Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04789395
Collaborator
(none)
25
1
15.6
1.6

Study Details

Study Description

Brief Summary

It is known that enhances wound healing by oxidative stress and supports immune system besides it is cheap and has not any side effects. Aim of the study is to prevent pulmonary fibrosis by using ozone therapy as a supportive therapy on the patients who have pneumonia and ground glass opacity on thorax CT both in ICU and wards. Patients will follow for a year.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The patients accepted with the diagnosis of pneumonia in Gaziosmanpaşa TREH, both in ICU and wards have treated with additional ozone therapy beside the normal treathments. In these patients the findings like ground glass opacity in thorax CT regarding to covid 19 were progressed or non changed. In the concern of these opacities turn to pulmonary fibrosis, ozone therapy has used to prevent this undesirable effect. It is known that enhances wound healing by oxidative stress and supports immune system besides it is cheap and has not any side effects.

    25 patients included this study. The patients were diagnosed with Covid-19 pneumonia and treated with ozone therapy in intensive care unit and ward. After treatment was done, findings of at least %20-25 ground-glass opacity on thorax ct were the main criteria for enrollment.

    The patients' follow-up program time after hospital discharge will be on 1st, 3rd, 6th and 12th month. They will continue to recieve ozon therapy once in a month during one year follow up. Ground-glass opacity rate of thorax ct scan will be recorded as less then %25, %25-50, %50-75 and above %75. Tomographies will be compared with each other and also last thorax ct before hospital discharge. These tomographies will be applied under 80 KV and this will give %40 less dosage according to routine 120 KV scans. If there is an increase in ground-glass opacities compared to the previous one, the scan will be done again on prone position and suspected lesions will be reevaluated. The pulmonary fibrosis findings of the scan will be diagnosed by a well trained radiology doctor. The evaluation of dyspnea will also done during follow-ups. mMRC(medical research council) dyspnea scale will be used for dyspnea status. SpO2 values in room-air will also recorded. FEV1, FVC and FEV1/FVC values will also be recorded to demonstrate respiratory functions.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    25 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Clinical Determination of Patients Who Intersive Care Unit and Clinical Ttreatments Have Finished Receive Ozonetheraphy With Thorax Tomography Regarding to Interstisial Fibrosis
    Actual Study Start Date :
    Sep 2, 2020
    Anticipated Primary Completion Date :
    Sep 20, 2021
    Anticipated Study Completion Date :
    Dec 20, 2021

    Outcome Measures

    Primary Outcome Measures

    1. prevention of pulmonary fibrosis in covid 19 pneumonia patients with ozone therapy [1 year]

      Ozone as an additional therapy can reduce the fibrosis

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • over 18 years covid 19 pneumonia patients who have ground glass opacity on thorax CT, receiving ozone as adjuvant therapy.
    Exclusion Criteria:
    • pregnant patients patients who doesnt treated with ozone(hyperthyroid,pulmonary hypertension, right ventricule failure,glucose 6 P dehydrogenase defficiency

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Gaziosmanpaşa TREH Istanbul Gaziosmanpaşa Turkey 34255

    Sponsors and Collaborators

    • Gaziosmanpasa Research and Education Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    SİBEL BEKTAŞ, director, Gaziosmanpasa Research and Education Hospital
    ClinicalTrials.gov Identifier:
    NCT04789395
    Other Study ID Numbers:
    • 08.092.r1.125
    First Posted:
    Mar 9, 2021
    Last Update Posted:
    Mar 9, 2021
    Last Verified:
    Mar 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by SİBEL BEKTAŞ, director, Gaziosmanpasa Research and Education Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 9, 2021