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Proactive Protection With Azithromycin and hydroxyChloroquine in Hospitalized Patients With COVID-19 (ProPAC-COVID)

Primary Purpose

Virus Diseases, Infection Viral, Corona Virus Infection

Status
Terminated
Phase
Phase 2
Locations
Denmark
Study Type
Interventional
Intervention
Azithromycin
Hydroxychloroquine
Placebo oral tablet
Placebo oral tablet
Sponsored by
Chronic Obstructive Pulmonary Disease Trial Network, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Virus Diseases

Eligibility Criteria

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

Inclusion Criteria:

  • Patient admitted to a Danish emergency department, lung medical department or medical department
  • Age >18 years
  • Hospitalized <48 hours
  • Positive COVID-19 test/diagnosis during the hospitalization
  • Signs informed consent

Exclusion Criteria:

  • If the patient uses > 5 LO2/min at time of recruitment
  • Known intolerance/allergy to azithromycin or hydroxychloroquine or hypersensitivity to quinine or 4-aminoquinolinderivates
  • Pregnancy
  • Breastfeeding
  • Neurogenic hearing loss
  • Psoriasis
  • Retinopathy
  • Maculopathy
  • Changes in vision field
  • Severe liver disease other than amoebiases
  • Severe gastrointestinal, neurological or haematological disorders
  • eGFR < 45 ml/min/1.73m2
  • Clinically significant cardiac conduction disorders/arrhythmias or prolonged QTc interval
  • Myasthenia Gravis
  • Uses Digoxin
  • Glucose-6-phosphate dehydrogenase deficiency
  • Porphyria
  • Hypoglycemia at any time since hospitalization
  • Severe mental illness which significantly impedes cooperation
  • Severe linguistic problems that significantly impedes cooperation
  • Treatment with sickle alkaloids

Sites / Locations

  • Aalborg Sygehus
  • Bispebjerg Hospital
  • Herlev-Gentofte Hospital
  • Hvidovre Hospital
  • Nordsjællands Hospital
  • Odense Universitetshospital
  • Roskilde Sygehus
  • Slagelse Sygehus

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Control

Intervention

Arm Description

This arm will receive standard care and placebo in 15 days. Azithromycin placebo: Day 1-3: 500 mg x 1 Day 4-15: 250 mg x 1 Hydroxychloroquine placebo: Day 1-15: 200 mg x 2

This arm will receive standard care and azithromycin and hydroxychloroquine in 15 days. Azithromycin: Day 1-3: 500 mg x 1 Day 4-15: 250 mg x 1 Hydroxychloroquine: Day 1-15: 200 mg x 2

Outcomes

Primary Outcome Measures

Number of Days Alive and Discharged From Hospital Within 14 Days

Secondary Outcome Measures

Categorization of Hospitalization Status
The patient will be categorized into one of the following 8 categories depending on status of their hospitalization: Dead (yes/no) Hospitalized and receiving mechanical ventilation or ExtraCorporalMembraneOxygenation (ECMO) (yes/no) Hospitalized and receiving Non-invasive ventilation or "high-flow oxygen device" (yes/no) Hospitalized and given oxygen supplements different from (2) and (3) (yes/no) Hospitalized and without oxygen treatment, but receiving other treatment (both related to COVID-19 or other) (yes/no) Hospitalized for observation (yes/no) Discharged from hospital with restriction of activity level (yes/no) Discharged from hospital without any restrictions of activity level (yes/no) Only one category can be "yes".
Length of Stay in ICU
Length of stay in intensive care unit.
Number of Participants on Non-invasive Ventilation (NIV) During Hospitalization
Mortality
Length of Hospitalization
Days Alive and Discharged From Hospital
Mortality
Mortality
Number of Readmissions (All Causes)
Number of Days Using Non-invasive Ventilation (NIV)
Number of days using non-invasive ventilation (NIV) if on NIV during hospitalization.
Change in Patient's Oxygen Partial Pressure
PaO2 measured in arterial puncture at baseline and 4 days.
Change in Patient's Carbondioxide Partial Pressure
PaCO2 measured in arterial puncture at baseline and 4 days.
Change of pH in Blood
pH measured in arterial puncture at baseline and 4 days.
Time for no Oxygen Supplement (or Regular Oxygen Supplement "LTOT")
Time for no oxygen supplement (or regular oxygen supplement "LTOT") if on oxygen during admission.

Full Information

First Posted
March 23, 2020
Last Updated
June 28, 2021
Sponsor
Chronic Obstructive Pulmonary Disease Trial Network, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT04322396
Brief Title
Proactive Protection With Azithromycin and hydroxyChloroquine in Hospitalized Patients With COVID-19
Acronym
ProPAC-COVID
Official Title
Proactive Protection With Azithromycin and Hydroxychloroquine in Hospitalized Patients With COVID: A Randomized, Placebo-controlled Double-blinded Trial Evaluating Treatment With Azithromycin and Hydroxychloroquine to Patients With COVID-19
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Terminated
Why Stopped
Recommended by the DSMB
Study Start Date
April 6, 2020 (Actual)
Primary Completion Date
February 2, 2021 (Actual)
Study Completion Date
February 2, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chronic Obstructive Pulmonary Disease Trial Network, Denmark

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
This study explores whether patients acutely hospitalized may have shorter hospitalization and fewer admittances at Intensive Care Units by treatment with azithromycin and hydroxychloroquine.
Detailed Description
In the ongoing coronavirus pandemic, COVID-19, that arose in Wuhan China, there is still sparse data in the course, risk of various complications, and in particular how patients who are hospitalized are best treated to ensure high survival and short hospitalization. Despite the rapid spread of the disease globally, there is no solid data yet to recommend any specific treatments, which is why symptomatic, organ supportive therapy including respiratory therapy in acute pulmonary failure is recommended. There has been reported a high incidence of bacterial super-infections in patients with COVID-19. Patients with COVID-19 also have a higher risk of dying because of septic shock. Thus, there is an urgent need for treatment that can improve the patient's chance of the shortest hospitalization possible, and treatment that can lower the risk of secondary infection and death. This is a randomized, placebo-controlled, double-blinded multi-center trial evaluating the effect of azithromycin and hydroxychloroquine treatment in patients with COVID-19 during hospitalization. The aim of the study is to investigate whether the treatment can shorten hospitalization, reduce the risk of non-invasive ventilation, admittance to Intensive Care Units and death.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Virus Diseases, Infection Viral, Corona Virus Infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
117 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
This arm will receive standard care and placebo in 15 days. Azithromycin placebo: Day 1-3: 500 mg x 1 Day 4-15: 250 mg x 1 Hydroxychloroquine placebo: Day 1-15: 200 mg x 2
Arm Title
Intervention
Arm Type
Active Comparator
Arm Description
This arm will receive standard care and azithromycin and hydroxychloroquine in 15 days. Azithromycin: Day 1-3: 500 mg x 1 Day 4-15: 250 mg x 1 Hydroxychloroquine: Day 1-15: 200 mg x 2
Intervention Type
Drug
Intervention Name(s)
Azithromycin
Intervention Description
Azithromycin
Intervention Type
Drug
Intervention Name(s)
Hydroxychloroquine
Intervention Description
Hydroxychloroquine
Intervention Type
Drug
Intervention Name(s)
Placebo oral tablet
Intervention Description
Placebo Azithromycin
Intervention Type
Drug
Intervention Name(s)
Placebo oral tablet
Intervention Description
Placebo Hydroxychloroquine
Primary Outcome Measure Information:
Title
Number of Days Alive and Discharged From Hospital Within 14 Days
Time Frame
14 days
Secondary Outcome Measure Information:
Title
Categorization of Hospitalization Status
Description
The patient will be categorized into one of the following 8 categories depending on status of their hospitalization: Dead (yes/no) Hospitalized and receiving mechanical ventilation or ExtraCorporalMembraneOxygenation (ECMO) (yes/no) Hospitalized and receiving Non-invasive ventilation or "high-flow oxygen device" (yes/no) Hospitalized and given oxygen supplements different from (2) and (3) (yes/no) Hospitalized and without oxygen treatment, but receiving other treatment (both related to COVID-19 or other) (yes/no) Hospitalized for observation (yes/no) Discharged from hospital with restriction of activity level (yes/no) Discharged from hospital without any restrictions of activity level (yes/no) Only one category can be "yes".
Time Frame
14 days
Title
Length of Stay in ICU
Description
Length of stay in intensive care unit.
Time Frame
14 days
Title
Number of Participants on Non-invasive Ventilation (NIV) During Hospitalization
Time Frame
14 days
Title
Mortality
Time Frame
30 days
Title
Length of Hospitalization
Time Frame
14 days
Title
Days Alive and Discharged From Hospital
Time Frame
30 days
Title
Mortality
Time Frame
90 days
Title
Mortality
Time Frame
365 days
Title
Number of Readmissions (All Causes)
Time Frame
30 days
Title
Number of Days Using Non-invasive Ventilation (NIV)
Description
Number of days using non-invasive ventilation (NIV) if on NIV during hospitalization.
Time Frame
14 days
Title
Change in Patient's Oxygen Partial Pressure
Description
PaO2 measured in arterial puncture at baseline and 4 days.
Time Frame
4 days
Title
Change in Patient's Carbondioxide Partial Pressure
Description
PaCO2 measured in arterial puncture at baseline and 4 days.
Time Frame
4 days
Title
Change of pH in Blood
Description
pH measured in arterial puncture at baseline and 4 days.
Time Frame
4 days
Title
Time for no Oxygen Supplement (or Regular Oxygen Supplement "LTOT")
Description
Time for no oxygen supplement (or regular oxygen supplement "LTOT") if on oxygen during admission.
Time Frame
14 days

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient admitted to a Danish emergency department, lung medical department or medical department Age >18 years Hospitalized <48 hours Positive COVID-19 test/diagnosis during the hospitalization Signs informed consent Exclusion Criteria: If the patient uses > 5 LO2/min at time of recruitment Known intolerance/allergy to azithromycin or hydroxychloroquine or hypersensitivity to quinine or 4-aminoquinolinderivates Pregnancy Breastfeeding Neurogenic hearing loss Psoriasis Retinopathy Maculopathy Changes in vision field Severe liver disease other than amoebiases Severe gastrointestinal, neurological or haematological disorders eGFR < 45 ml/min/1.73m2 Clinically significant cardiac conduction disorders/arrhythmias or prolonged QTc interval Myasthenia Gravis Uses Digoxin Glucose-6-phosphate dehydrogenase deficiency Porphyria Hypoglycemia at any time since hospitalization Severe mental illness which significantly impedes cooperation Severe linguistic problems that significantly impedes cooperation Treatment with sickle alkaloids
Facility Information:
Facility Name
Aalborg Sygehus
City
Aalborg
Country
Denmark
Facility Name
Bispebjerg Hospital
City
Copenhagen
Country
Denmark
Facility Name
Herlev-Gentofte Hospital
City
Copenhagen
Country
Denmark
Facility Name
Hvidovre Hospital
City
Copenhagen
Country
Denmark
Facility Name
Nordsjællands Hospital
City
Hillerød
Country
Denmark
Facility Name
Odense Universitetshospital
City
Odense
Country
Denmark
Facility Name
Roskilde Sygehus
City
Roskilde
Country
Denmark
Facility Name
Slagelse Sygehus
City
Slagelse
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
33081817
Citation
Sivapalan P, Ulrik CS, Lappere TS, Eklof JV, Shaker SB, Bodtger UCS, Browatzki A, Meyer CN, Weinreich UM, Laursen CB, Biering-Sorensen T, Knop FK, Lundgren JD, Jensen JS. Proactive prophylaxis with azithromycin and hydroxychloroquine in hospitalized patients with COVID-19 (ProPAC-COVID): a statistical analysis plan. Trials. 2020 Oct 20;21(1):867. doi: 10.1186/s13063-020-04795-0.
Results Reference
derived
PubMed Identifier
32522282
Citation
Sivapalan P, Ulrik CS, Bojesen RD, Lapperre TS, Eklof JV, Hakansson KEJ, Browatzki A, Tidemansen C, Wilcke JT, Janner J, Gottlieb V, Meteran H, Porsbjerg C, Madsen BL, Moberg M, Pedersen L, Benfield TL, Lundgren JD, Knop FK, Biering-Sorensen T, Ghanizada M, Sonne TP, Bodtger UCS, Jensen SG, Rasmussen DB, Brondum E, Tupper OD, Sorensen SW, Alstrup G, Laursen CB, Moller UW, Sverrild A, Jensen JS. Proactive Prophylaxis With Azithromycin and HydroxyChloroquine in Hospitalised Patients With COVID-19 (ProPAC-COVID): A structured summary of a study protocol for a randomised controlled trial. Trials. 2020 Jun 10;21(1):513. doi: 10.1186/s13063-020-04409-9.
Results Reference
derived

Learn more about this trial

Proactive Protection With Azithromycin and hydroxyChloroquine in Hospitalized Patients With COVID-19

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