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Colchicine Counteracting Inflammation in COVID-19 Pneumonia (ColCOVID-19)

Primary Purpose

Coronavirus Infections, Pneumonia, Viral

Status
Completed
Phase
Phase 2
Locations
Italy
Study Type
Interventional
Intervention
Colchicine
Sponsored by
Azienda Ospedaliero-Universitaria di Parma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronavirus Infections focused on measuring Colchicine, Corona Virus Infection, COVID-19

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Positive nasopharyngeal swab for COVID-19, asymptomatic or paucisymptomatic, aged ≥70 years and/or with clinical risk factors for poor outcome (clinically relevant chronic lung disease, diabetes and/or heart disease) or
  • symptomatic with respiratory or systemic symptoms, however clinically stable (MEWS<3) with CT imaging showing viral pneumonia and positive or pending pharyngo-nasal swab for COVID-19: Temperature 38°C and/or intensive cough, Respiratory rate < 25 /min, oxygen saturation (pulse oximetry) >95%
  • Positive swab for COVID-19
  • with respiratory and/or systemic symptoms and initial mild respiratory failure e with objective signs of lung involvement; the patient is in stable conditions (MEWS < 3) Temperature>38°C and or intensive cough, Respiratory rate ≥25 /min, or oxygen saturation 94- 95% in room air

Exclusion Criteria:

  • Pregnant or breast feeding
  • MEWS >=3
  • Hepatic failure Child-Pugh C
  • Enrollment in other pharmacological studies
  • Ongoing treatment with colchicine
  • Ongoing treatment with antiviral drugs that include ritonavir or cobicistat
  • Any medical condition or disease which in the opinion of the Investigator may place the patient at unacceptable risk for study participation.

Sites / Locations

  • Azienda Ospedaliero Universitaria di Parma

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Colchicine

Standard of care

Arm Description

Administration of Colchicine 1mg (or 0.5 mg in CKD)/day + standard of care for COVID-19 pneumonia

Standard of care for COVID-19 pneumonia

Outcomes

Primary Outcome Measures

Clinical improvement
Time to clinical improvement: defined as time from randomization to an improvement of two points from the status at randomization on a seven-category ordinary scale
Hospital discharge
Live discharge from the hospital (whatever comes first)

Secondary Outcome Measures

Death
Number of death patients
Clinical status
7-category ordinal scale
Mechanical ventilhation
Number of patients with mechanical ventilhation
Hospitalization
Days of hospitalization
Time from treatment initiation to death
Days to death from treatment initiation
Time to Negativization COVID 19
negativization of two consecutive pharyngo-nasal swab 24-72 hrs apart
Fever
Time to remission of fever in patients with T>37.5°C at enrollment

Full Information

First Posted
March 24, 2020
Last Updated
July 19, 2022
Sponsor
Azienda Ospedaliero-Universitaria di Parma
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1. Study Identification

Unique Protocol Identification Number
NCT04322565
Brief Title
Colchicine Counteracting Inflammation in COVID-19 Pneumonia
Acronym
ColCOVID-19
Official Title
Colchicine to Counteract Inflammatory Response in COVID-19 Pneumonia
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
April 20, 2020 (Actual)
Primary Completion Date
September 1, 2021 (Actual)
Study Completion Date
October 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda Ospedaliero-Universitaria di Parma

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
Yes

5. Study Description

Brief Summary
Cytokines and chemokines are thought to play an important role in immunity and immunopathology during virus infections [3]. Patients with severe COVID-19 have higher serum levels of pro-inflammatory cytokines (TNF-α, IL-1 and IL-6) and chemokines (IL-8) compared to individuals with mild disease or healthy controls, similar to patients with SARS or MERS . The change of laboratory parameters, including elevated serum cytokine, chemokine levels, and increased NLR in infected patients are correlated with the severity of the disease and adverse outcome, suggesting a possible role for hyper-inflammatory responses in COVID-19 pathogenesis. Importantly, previous studies showed that viroporin E, a component of SARS-associated coronavirus (SARS-CoV), forms Ca2C-permeable ion channels and activates the NLRP3 inflammasome. In addition, another viroporin 3a was found to induce NLRP3 inflammasome activation . The mechanisms are unclear. Colchicine, an old drug used in auto-inflammatory disorders (i.e., Familiar Mediterranean Fever and Bechet disease) and in gout, counteracts the assembly of the NLRP3 inflammasome, thereby reducing the release of IL-1b and an array of other interleukins, including IL-6, that are formed in response to danger signals. Recently, colchicine has been successfully used in two cases of life-threatening post-transplant capillary leak syndrome. These patients had required mechanically ventilation for weeks and hemodialysis, before receiving colchicine, which abruptly restored normal respiratory function and diuresis over 48 hrs [4].

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronavirus Infections, Pneumonia, Viral
Keywords
Colchicine, Corona Virus Infection, COVID-19

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
193 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Colchicine
Arm Type
Experimental
Arm Description
Administration of Colchicine 1mg (or 0.5 mg in CKD)/day + standard of care for COVID-19 pneumonia
Arm Title
Standard of care
Arm Type
No Intervention
Arm Description
Standard of care for COVID-19 pneumonia
Intervention Type
Drug
Intervention Name(s)
Colchicine
Intervention Description
Cochicine 1mg/day
Primary Outcome Measure Information:
Title
Clinical improvement
Description
Time to clinical improvement: defined as time from randomization to an improvement of two points from the status at randomization on a seven-category ordinary scale
Time Frame
Day 28
Title
Hospital discharge
Description
Live discharge from the hospital (whatever comes first)
Time Frame
Day 28
Secondary Outcome Measure Information:
Title
Death
Description
Number of death patients
Time Frame
Day 28
Title
Clinical status
Description
7-category ordinal scale
Time Frame
Day 7, Day 14
Title
Mechanical ventilhation
Description
Number of patients with mechanical ventilhation
Time Frame
Day 28
Title
Hospitalization
Description
Days of hospitalization
Time Frame
Day 28
Title
Time from treatment initiation to death
Description
Days to death from treatment initiation
Time Frame
Day 28
Title
Time to Negativization COVID 19
Description
negativization of two consecutive pharyngo-nasal swab 24-72 hrs apart
Time Frame
Day 21
Title
Fever
Description
Time to remission of fever in patients with T>37.5°C at enrollment
Time Frame
Day 1,4,7,14,21,28

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Positive nasopharyngeal swab for COVID-19, asymptomatic or paucisymptomatic, aged ≥70 years and/or with clinical risk factors for poor outcome (clinically relevant chronic lung disease, diabetes and/or heart disease) or symptomatic with respiratory or systemic symptoms, however clinically stable (MEWS<3) with CT imaging showing viral pneumonia and positive or pending pharyngo-nasal swab for COVID-19: Temperature 38°C and/or intensive cough, Respiratory rate < 25 /min, oxygen saturation (pulse oximetry) >95% Positive swab for COVID-19 with respiratory and/or systemic symptoms and initial mild respiratory failure e with objective signs of lung involvement; the patient is in stable conditions (MEWS < 3) Temperature>38°C and or intensive cough, Respiratory rate ≥25 /min, or oxygen saturation 94- 95% in room air Exclusion Criteria: Pregnant or breast feeding MEWS >=3 Hepatic failure Child-Pugh C Enrollment in other pharmacological studies Ongoing treatment with colchicine Ongoing treatment with antiviral drugs that include ritonavir or cobicistat Any medical condition or disease which in the opinion of the Investigator may place the patient at unacceptable risk for study participation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Umberto Maggiore, MD
Organizational Affiliation
Azienda Ospedaliero-Universitaria di Parma
Official's Role
Principal Investigator
Facility Information:
Facility Name
Azienda Ospedaliero Universitaria di Parma
City
Parma
State/Province
PR
ZIP/Postal Code
43100
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Time Frame
Data will be avaliable from July 2020 and documentation will be shared for 10 years
IPD Sharing Access Criteria
The sponsor recognizes the importance of communicating study data and will disclose and publish the results in a suitable form regardless of outcome. The sponsor will publish the results of this study in scientific journals
Citations:
PubMed Identifier
34658014
Citation
Mikolajewska A, Fischer AL, Piechotta V, Mueller A, Metzendorf MI, Becker M, Dorando E, Pacheco RL, Martimbianco ALC, Riera R, Skoetz N, Stegemann M. Colchicine for the treatment of COVID-19. Cochrane Database Syst Rev. 2021 Oct 18;10(10):CD015045. doi: 10.1002/14651858.CD015045.
Results Reference
derived

Learn more about this trial

Colchicine Counteracting Inflammation in COVID-19 Pneumonia

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