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STerOids in COVID-19 Study (STOIC)

Primary Purpose

Coronavirus Infection

Status
Terminated
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Budesonide dry powder inhaler
Sponsored by
University of Oxford
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronavirus Infection focused on measuring CoVID-19, Coronavirus infection, SARS-CoV-2

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Participant is willing and able to give informed consent for participation in the trial
  • Male or Female, aged 18 years or above
  • New onset of symptoms suggestive of COVID-19 e.g. new onset cough and/or fever, and/or loss of smell or taste within 7 or fewer days of participant being seen at visit 1
  • In the Investigator's opinion, is able and willing to comply with all trial requirements

Exclusion Criteria:

  • A known allergy to investigational medicine product (IMP) (budesonide)
  • Any known contraindication to any of the IMPs (budesonide)
  • Patient currently prescribed inhaled or systemic corticosteroids
  • Recent use, within the previous 7 days of inhaled or systemic corticosteroids
  • Patient needs hospitalisation at time of study consent
  • Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial.
  • Participants who have participated in another research trial involving an investigational product in the past 12 weeks.

Sites / Locations

  • Oxford Respiratory Trials Unit

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Inhaled budesonide

Standard of care

Arm Description

Budesonide inhaled via dry powder inhaler, 400 micrograms per inhalation, 2 inhalations twice a day

Standard of care

Outcomes

Primary Outcome Measures

Emergency department attendance of hospitalisation related to COVID-19
Evaluate the effect of intervention on emergency department attendance or hospitalisation related to COVID-19

Secondary Outcome Measures

Body temperature
Evaluate the effect of intervention on body temperature
Blood oxygen saturation level
Evaluate the effect of intervention on blood oxygen level
Symptoms as assessed by common cold questionnaire
Evaluate the effect of intervention on patient's symptoms as determined by common cold questionnaire. Higher score meaning worse symptoms.
Symptoms as assessed by FluPro questionnaire
Evaluate the effect of intervention on patient's symptoms as determined by FluPro questionnaire. Higher score meaning worse symptoms.
Nasal/throat swab SARS-CoV-2 viral load
Evaluate the effect of intervention on nasal and throat swab SARS-CoV-2 viral load

Full Information

First Posted
June 3, 2020
Last Updated
February 3, 2021
Sponsor
University of Oxford
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1. Study Identification

Unique Protocol Identification Number
NCT04416399
Brief Title
STerOids in COVID-19 Study
Acronym
STOIC
Official Title
Use of High Dose Inhaled Corticosteroids as Treatment of Early COVID-19 Infection to Prevent Clinical Deterioration and Hospitalisation
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Terminated
Why Stopped
Independent statistical review advice
Study Start Date
July 16, 2020 (Actual)
Primary Completion Date
January 12, 2021 (Actual)
Study Completion Date
January 12, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Oxford

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
At the time of writing (3/4/2020), close to a million people have been infected by the SARS-CoV-2 coronavirus around the world. The severe clinical condition that leads to deaths is now called CoVID-19. Currently, there are no effective treatments for the early or late stages of this illness. Governments worldwide have undertaken dramatic interventions to try and reduce the rate of spread of this deadly coronavirus. Early data from multiple studies in China, where the virus originated, show that severe cases of CoVID-19 are not as prevalent in patients with chronic lung diseases as expected. This data has been confirmed by the Italian physicians. The investigators think that the widespread use of inhaled corticosteroids reduces the risk of CoVID-19 pneumonia in patients with chronic lung disease. Early microbiological data also shows that these corticosteroids are effective at slowing down the rate of coronavirus replication on lung cells. Inhaled corticosteroids are widely used to manage common lung conditions, such as asthma. This type of medicine is among the top 3 most common medication prescribed around the world. Their safety is well understood, and their potential side effects are mild and reversible. The investigators propose to test this idea that, in participants early in the course of CoVID-19 illness, daily high dose inhaled corticosteroids for 28 days, will reduce the chances of severe respiratory illness needing hospitalisation. We will also study the effect of this inhaled therapy on symptoms and viral load.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronavirus Infection
Keywords
CoVID-19, Coronavirus infection, SARS-CoV-2

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Randomised, open label parallel group controlled clinical trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
146 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Inhaled budesonide
Arm Type
Experimental
Arm Description
Budesonide inhaled via dry powder inhaler, 400 micrograms per inhalation, 2 inhalations twice a day
Arm Title
Standard of care
Arm Type
No Intervention
Arm Description
Standard of care
Intervention Type
Drug
Intervention Name(s)
Budesonide dry powder inhaler
Other Intervention Name(s)
Pulmicort
Intervention Description
Budesonide inhaled via dry powder inhaler, 400 micrograms per inhalation, 2 inhalations twice a day
Primary Outcome Measure Information:
Title
Emergency department attendance of hospitalisation related to COVID-19
Description
Evaluate the effect of intervention on emergency department attendance or hospitalisation related to COVID-19
Time Frame
Day 1 to day 28
Secondary Outcome Measure Information:
Title
Body temperature
Description
Evaluate the effect of intervention on body temperature
Time Frame
Day 1 to day 14
Title
Blood oxygen saturation level
Description
Evaluate the effect of intervention on blood oxygen level
Time Frame
Day 1 to day 14
Title
Symptoms as assessed by common cold questionnaire
Description
Evaluate the effect of intervention on patient's symptoms as determined by common cold questionnaire. Higher score meaning worse symptoms.
Time Frame
Day 1 to day 14
Title
Symptoms as assessed by FluPro questionnaire
Description
Evaluate the effect of intervention on patient's symptoms as determined by FluPro questionnaire. Higher score meaning worse symptoms.
Time Frame
Day 1 to day 14
Title
Nasal/throat swab SARS-CoV-2 viral load
Description
Evaluate the effect of intervention on nasal and throat swab SARS-CoV-2 viral load
Time Frame
Day 1, 7 and 14

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participant is willing and able to give informed consent for participation in the trial Male or Female, aged 18 years or above New onset of symptoms suggestive of COVID-19 e.g. new onset cough and/or fever, and/or loss of smell or taste within 7 or fewer days of participant being seen at visit 1 In the Investigator's opinion, is able and willing to comply with all trial requirements Exclusion Criteria: A known allergy to investigational medicine product (IMP) (budesonide) Any known contraindication to any of the IMPs (budesonide) Patient currently prescribed inhaled or systemic corticosteroids Recent use, within the previous 7 days of inhaled or systemic corticosteroids Patient needs hospitalisation at time of study consent Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial. Participants who have participated in another research trial involving an investigational product in the past 12 weeks.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mona Bafadhel, MBBS, PhD
Organizational Affiliation
University of Oxford
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oxford Respiratory Trials Unit
City
Oxford
State/Province
Oxfordshire
ZIP/Postal Code
OX3 7LE
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35397798
Citation
Baker JR, Mahdi M, Nicolau DV Jr, Ramakrishnan S, Barnes PJ, Simpson JL, Cass SP, Russell REK, Donnelly LE, Bafadhel M. Early Th2 inflammation in the upper respiratory mucosa as a predictor of severe COVID-19 and modulation by early treatment with inhaled corticosteroids: a mechanistic analysis. Lancet Respir Med. 2022 Jun;10(6):545-556. doi: 10.1016/S2213-2600(22)00002-9. Epub 2022 Apr 7. Erratum In: Lancet Respir Med. 2022 Jun;10(6):e60.
Results Reference
derived
PubMed Identifier
33844996
Citation
Ramakrishnan S, Nicolau DV Jr, Langford B, Mahdi M, Jeffers H, Mwasuku C, Krassowska K, Fox R, Binnian I, Glover V, Bright S, Butler C, Cane JL, Halner A, Matthews PC, Donnelly LE, Simpson JL, Baker JR, Fadai NT, Peterson S, Bengtsson T, Barnes PJ, Russell REK, Bafadhel M. Inhaled budesonide in the treatment of early COVID-19 (STOIC): a phase 2, open-label, randomised controlled trial. Lancet Respir Med. 2021 Jul;9(7):763-772. doi: 10.1016/S2213-2600(21)00160-0. Epub 2021 Apr 9. Erratum In: Lancet Respir Med. 2021 Jun;9(6):e55.
Results Reference
derived
PubMed Identifier
33388170
Citation
Farne H, Singanayagam A. Reply. J Allergy Clin Immunol. 2021 Mar;147(3):1117-1118. doi: 10.1016/j.jaci.2020.11.019. Epub 2020 Dec 30. No abstract available.
Results Reference
derived
PubMed Identifier
32738928
Citation
Nicolau DV, Bafadhel M. Inhaled corticosteroids in virus pandemics: a treatment for COVID-19? Lancet Respir Med. 2020 Sep;8(9):846-847. doi: 10.1016/S2213-2600(20)30314-3. Epub 2020 Jul 30. No abstract available.
Results Reference
derived

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STerOids in COVID-19 Study

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