MedPath

ow dose Radiotherapy for COVID-19 using Linear accelerator

Phase 2
Conditions
Health Condition 1: - Health Condition 2: B972- Coronavirus as the cause of diseases classified elsewhere
Registration Number
CTRI/2021/05/033883
Lead Sponsor
Surya Global Multi Speciality Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Adult patients with RT-PCR proven COVID-19 with moderate to severe pneumonia with fewer than 14 days of symptom onset that

warranted hospitalization and currently receiving standard medication for COVID-19 at appropriate doses which would include,among others, antivirals, corticosteroids, or anti-IL-6 tocilizumab.and

2. moderate to severe dyspnoea, respiratory frequency equal to or greater than 30/min, oxygen saturation without supplemental O2

supply SpO2 94% or less, PaO2/FiO2 ratio or PaFiO2 ratio between 200 to 300 or SpO2/FiO2 ratio 315 or less if PaO2 is not available

and/or

3. laboratory abnormalities such as C-reactive protein >100 mg/L or D-dimer >1000 ng/ml or IL-6 >50 IU or suspected cytokine release

syndrome

Exclusion Criteria

1. Patients on ventilators (invasive/non invasive)

2. Prior lobectomy or pneumonectomy

3. Prior thoracic radiotherapy resulting in a maximum lung dose of 100 cGy or higher within 14 days of enrollment

4. Prior chemotherapy or other systemic therapy with potential for pulmonary toxicity or radio sensitization within 14 days or 5 half-lives,

whichever is greater, of enrollment, e.g., bleomycin, gemcitabine

5. Prior cancer immunotherapy with an immune checkpoint inhibitor within 60 days of enrollment

6. Severe pre-existing heart disease, e.g., New York Heart Association (NYHA) functional class 3 (or higher) congestive heart failure

7. History of bone marrow or solid organ transplantation

8. Known history of autoimmune collagen vascular disease, e.g.,scleroderma

9. Known hereditary syndrome with increased sensitivity to ionizing radiation, e.g., ataxia-telangiectasia or Fanconi anemia

10. Pregnancy

11. Inability to be positioned supine and flat for radiation planning and delivery

12. Inability to provide informed consent or lack of an authorized representative who can provide informed consent

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath