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Post Exposure Prophylaxis in Healthcare Workers Exposed to COVID-19 Patients (HCQ-COVID19)

Primary Purpose

COVID 19

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Hydroxychloroquine
Sponsored by
Hamad Medical Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for COVID 19 focused on measuring Hydroxychloroquine, Coronavirus Disease 2019, Post Exposure Prophylaxis, Center for Disease Control and Prevention, Coded Record Form

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 18 years or older, all healthcare workers in direct contact with COVID-19 patients (ex: physicians, nurses, pharmacists, etc.), the ability to swallow Oral medications, without any GI abnormalities that may affect absorption. Who agree to participate in the trial.

Exclusion Criteria:

  • Allergy to HCQ.
  • Pregnancy or breastfeeding.
  • Known history of Retinal disease not related to Macular degeneration, or preexisting eye retinopathy.
  • Having a prior history of blood disorders such as aplastic anemia, agranulocytosis, leukopenia, or thrombocytopenia.
  • Having a prior history of glucose-6-phosphate dehydrogenase (G-6-PD) deficiency.
  • Having dermatitis, psoriasis, or porphyria.
  • History of lung disease or Pneumonia not related to COVID-19.
  • Taking CYP450 enzyme-inducing medications within 4 weeks of the start of taking HCQ (Ex: Phenytoin, Carbamazepine, Phenobarbital, Primidone or Oxcarbazepine.
  • Currently taking QT-prolonging medications, which may include Antiarrhythmics, Quinolones, Macrolides, select Antipsychotics and Antidepressants.
  • Team members planning to have major abdominal, thoracic, spine or CNS surgery during the protocol period

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Hydroxychloroquine

    Placebo

    Arm Description

    400mg twice a day on day 1 followed by 400 mg weekly for 7 weeks.

    2 tablets (Placebo White tablets) twice daily on day 1 followed by 2 tablets weekly for 7 weeks

    Outcomes

    Primary Outcome Measures

    Prevention of SARS-CoV-2 infection
    Prevention of SARS-CoV-2 infection as determined by negative RT-PCR of the participants in the treatment group through swabbing that will be conducted on a weekly basis (Swabbing will be conducted at baseline and weekly through the end of the treatment period
    Presence of any adverse effects related to HCQ
    To find out the adverse effects related to HCQ such as : skin rashes, especially those made worse by sunlight, feeling sick (nausea) or indigestion, diarrhea, headaches, bleaching of the hair or mild hair loss, tinnitus (ringing in the ears) visual problem
    Incidence of COVID-19 related symptoms
    Incidence of COVID-19 related symptoms, that may include: Temperature over 37.8 degrees Celsius, Shortness of Breath, Cough.

    Secondary Outcome Measures

    Full Information

    First Posted
    June 17, 2020
    Last Updated
    August 7, 2020
    Sponsor
    Hamad Medical Corporation
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04437693
    Brief Title
    Post Exposure Prophylaxis in Healthcare Workers Exposed to COVID-19 Patients
    Acronym
    HCQ-COVID19
    Official Title
    Post Exposure Prophylaxis (PEP) in Healthcare Workers Exposed to COVID-19 Patients: A Double-blind Randomized Clinical Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    August 31, 2020 (Anticipated)
    Primary Completion Date
    August 30, 2021 (Anticipated)
    Study Completion Date
    December 31, 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Hamad Medical Corporation

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    More cases of COVID-19 pandemic are being reported daily around the world. It is highly infectious and, over 7 million people have been infected and more than 400,000 people have died globally till this date. Countries around the world are struggling to avoid the spread of this pandemic. Center for Disease Control and Prevention (CDC) confirmed that there are no approved drugs for COVID-19 treatment. Researchers around the globe, however, are researching different medications for COVID-19 patients, including the drug Hydroxychloroquine (HCQ), which is mainly used for Rheumatoid Arthritis and Malaria. Not enough data was obtained yet to know how well all of these medications are functioning. Therefore, aim to perform a randomized placebo-controlled trial to assess the impact of these medications on COVID -19 healthcare workers exposed while treating COVID 19 patients in Qatar to avoid causality and comorbidities in healthcare workers. It is considered as a weak base. Many viruses enter the host cells via endocytosis, as a result of which they are initially taken up into an intracellular compartment that is "typically fairly acidic" whereas; Hydroxychloroquine would alter the acidity of this compartment, which can interfere with the ability of viruses to escape into the host cell and start replicating. Another hypothesis on the rationale of the Antiviral activity of HCQ, is that HCQ may also alter the ability of the virus to bind to the outside of a host cell in the first place. An interventional, double-blind, placebo-controlled randomized trial that will include participants who will be healthcare workers at risks of exposure to COVID-19 while managing patients with confirmed infection. Study will compare the safety, efficacy and effectiveness of Post Exposure Prophylaxis (PEP) use of HCQ in healthcare workers at risk of exposure to COVID-19 patients, in comparison to Placebo in Qatar.
    Detailed Description
    More cases of COVID-19 pandemic are being reported daily around the world. It is highly infectious and, over 7 million people have been infected and more than 400,000 people have died globally till this date. Countries around the world are struggling to avoid the spread of this pandemic. The most common symptoms of coronavirus disease are fever, fatigue, and dry cough. Most people (approximately 80 percent) recover from the disease without special care. The disease can be serious, and even fatal. Older people, and people with other medical conditions (such as asthma, diabetes, or heart disease), maybe more vulnerable to becoming severely ill. As the COVID-19 pandemic continues to affect communities throughout the world, the search for effective drugs remains a priority. Scientists across the globe are working to produce a vaccine, but unlikely to be available before 2021. Meanwhile, a growing number of countries have taken a series of systematic measures to curb coronavirus spread, including national lockdowns, meeting bans, school closings, closures of restaurants, bars, sports clubs etc Researchers used to evaluate the invitro effectiveness of several potential COVID-19 treatments, including chloroquine (CQ) and redmeveir (RDV). The findings were found encouraging as 90 percent of the virus was inhibited by a low concentration of CQ and the results for RDV were even better-with an even lower concentration of this drug, achieving a virus inhibition of 90 percent. However, unless clinically verified, it cannot confirm these drugs for the treatment of COVID-19 patients. It is not known how well these medications function in people who are infected with COVID-19 and is still being studied. The first patient reported to be infected with COVID -19 in the U.S. was treated with RDV. The treatment started on the 7th day of hospitalization and on the 11th day after his symptoms were first identified. He started showing signs of progress on the very next day, presumably due to treatment with RDV. Further data, however, is required to confirm the effect of this treatment. Researchers in France have also been studying the effectiveness of hydroxychloroquine (HCQ) in a single-arm regimen to treat people with COVID-19. HCQ (and, in some cases, also antibiotic azithromycin) has been used in this study to treat individuals with the COVID-19 virus in one setting. Investigators measured the amount of virus in swabs taken from these individuals and from a group of individuals who did not receive HCQ. A larger decrease in the volume of the virus from the individuals receiving HCQ occurred on a span of six days. However, the groups were not randomized. Individuals who did not receive HCQ were at various medical facilities and not necessarily like the individuals in the HCQ group. The results are intriguing. But it's important to note that scientists have expressed concerns about this study. Indeed, after the publication of these findings, a statement has been released in the journal that it did not meet the "expected standard" of research (6). Moreover, these two drugs HCQ and RDV were designed primarily to fight other diseases and not COVID-19. Few data are available indicating that either could have some interest in the treatment of the disease, but its complete effect on COVID-19 patients is not known. One reason why researchers are interested in this drug is the HCQ's ability to modulate the inflammatory response. Inflammation is the natural reaction of the body to bacteria, viruses, or other substances that attack it. Our immune system usually attacks and actively kills infected cells or foreign bodies. But this response may often fail to function properly particularly in autoimmune disorders where the body is mistakenly attacking itself. HCQ has subtle effects on a wide variety of immune cells, and it may be that one of these effects helps stimulate the body's ability to fight off Covid-19. The inflammatory response in COVID-19 can be so strong that it causes serious damage to the lungs, that is why patients with severe infections need ventilators Another hypothesis on the rationale of the Antiviral activity of HCQ, is that HCQ may also alter the ability of the virus to bind to the outside of a host cell in the first place. The gold standard of a drug trial is a placebo-controlled, randomized, double-blind study. One group of participants should receive the investigational drug and another group should receive a placebo. The individuals in each arm of the study should be randomized; the demographics of both groups should be similar. Finally, the participants should not know if they are receiving the investigational drug or a placebo and the healthcare workers should not know what they are administering. Only under these conditions, It can conclusively determine the safety and efficacy of a potential treatment. Center for Disease Control and Prevention (CDC) confirmed that there are no approved drugs for COVID-19 treatment. Researchers around the globe, however, are researching different medications for COVID-19 patients, including the drug Hydroxychloroquine, which is mainly used for the treatment of Rheumatoid Arthritis and Malaria. Not enough data was obtained yet to know how well all of these medications are functioning. Therefore, aim to perform a randomized placebo-controlled trial to assess the impact of these medications on healthcare workers who exposed for the treatment of COVID -19 patients in Qatar. Rational to conduct a clinical trial on HCQ: It is considered as a weak base. Many viruses enter the host cells via endocytosis, as a result of which they are initially taken up into an intracellular compartment that is "typically fairly acidic" whereas; Hydroxychloroquine would alter the acidity of this compartment, which can interfere with the ability of viruses to escape into the host cell and start replicating. Another hypothesis on the rationale of the Antiviral activity of HCQ, is that HCQ may also alter the ability of the virus to bind to the outside of a host cell in the first place. Hypothesis: HCQ will be more safe and effective in comparison to placebo in the prevention of COVID 19 cases, in healthcare workers exposed to COVID 19 patients.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    COVID 19
    Keywords
    Hydroxychloroquine, Coronavirus Disease 2019, Post Exposure Prophylaxis, Center for Disease Control and Prevention, Coded Record Form

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 2, Phase 3
    Interventional Study Model
    Parallel Assignment
    Model Description
    An interventional, double-blind, placebo-controlled randomized trial
    Masking
    Participant
    Masking Description
    The process of keeping the study group assignment hidden after allocation will be used where the investigator and participants will be unaware of the drug.A double blind randomized clinical trial has been proposed having 250 subjects in each arm. 500 subjects will be selected using randomly permuted blocks of 2,4, and 8 for the random process to allocate subjects into the two groups equally by using computer software.
    Allocation
    Randomized
    Enrollment
    500 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Hydroxychloroquine
    Arm Type
    Experimental
    Arm Description
    400mg twice a day on day 1 followed by 400 mg weekly for 7 weeks.
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    2 tablets (Placebo White tablets) twice daily on day 1 followed by 2 tablets weekly for 7 weeks
    Intervention Type
    Drug
    Intervention Name(s)
    Hydroxychloroquine
    Other Intervention Name(s)
    Placebo
    Intervention Description
    The treatment group that will receive Hydroxychloroquine (HCQ) 400mg twice a day on day 1 followed by 400 mg weekly for 7 weeks
    Primary Outcome Measure Information:
    Title
    Prevention of SARS-CoV-2 infection
    Description
    Prevention of SARS-CoV-2 infection as determined by negative RT-PCR of the participants in the treatment group through swabbing that will be conducted on a weekly basis (Swabbing will be conducted at baseline and weekly through the end of the treatment period
    Time Frame
    7 Months
    Title
    Presence of any adverse effects related to HCQ
    Description
    To find out the adverse effects related to HCQ such as : skin rashes, especially those made worse by sunlight, feeling sick (nausea) or indigestion, diarrhea, headaches, bleaching of the hair or mild hair loss, tinnitus (ringing in the ears) visual problem
    Time Frame
    7 months
    Title
    Incidence of COVID-19 related symptoms
    Description
    Incidence of COVID-19 related symptoms, that may include: Temperature over 37.8 degrees Celsius, Shortness of Breath, Cough.
    Time Frame
    7 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: 18 years or older, all healthcare workers in direct contact with COVID-19 patients (ex: physicians, nurses, pharmacists, etc.), the ability to swallow Oral medications, without any GI abnormalities that may affect absorption. Who agree to participate in the trial. Exclusion Criteria: Allergy to HCQ. Pregnancy or breastfeeding. Known history of Retinal disease not related to Macular degeneration, or preexisting eye retinopathy. Having a prior history of blood disorders such as aplastic anemia, agranulocytosis, leukopenia, or thrombocytopenia. Having a prior history of glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. Having dermatitis, psoriasis, or porphyria. History of lung disease or Pneumonia not related to COVID-19. Taking CYP450 enzyme-inducing medications within 4 weeks of the start of taking HCQ (Ex: Phenytoin, Carbamazepine, Phenobarbital, Primidone or Oxcarbazepine. Currently taking QT-prolonging medications, which may include Antiarrhythmics, Quinolones, Macrolides, select Antipsychotics and Antidepressants. Team members planning to have major abdominal, thoracic, spine or CNS surgery during the protocol period
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Nasser Al Ansari, FRCPath
    Phone
    33554409
    Email
    nalansari2@hamad.qa
    First Name & Middle Initial & Last Name or Official Title & Degree
    Rajvir Singh, Ph.D.
    Phone
    55897044
    Email
    rsingh@hamad.qa
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Nasser Al Ansari, FRCPath
    Organizational Affiliation
    Hamad Medical Corporation (HMC)
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    There is a plan to make IPD and related data dictionaries available.
    IPD Sharing Time Frame
    One year
    IPD Sharing Access Criteria
    2021 to 2025
    Available IPD and Supporting Information:
    Available IPD/Information Type
    Clinical Study Report
    Available IPD/Information URL
    https://www.worldometers.info/coronavirus/
    Available IPD/Information Comments
    https://www.worldometers.info/coronavirus/
    Available IPD/Information Type
    Clinical Study Report
    Available IPD/Information URL
    https://www.who.int/docs/default-source/coronaviruse/who-china-joint-mission-on-covid-19-final-report.pdf
    Available IPD/Information Comments
    https://www.who.int/docs/default-source/coronaviruse/who-china-joint-mission-on-covid-19-final-report.pdf

    Learn more about this trial

    Post Exposure Prophylaxis in Healthcare Workers Exposed to COVID-19 Patients

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