PREPCOV: Efficacy of Pre-exposure Treatment With Hydroxy-Chloroquine on the Risk and Severity of COVID-19 Infection

Sponsor
University Hospital, Toulouse (Other)
Overall Status
Recruiting
CT.gov ID
NCT04481633
Collaborator
(none)
800
12
2
17.7
66.7
3.8

Study Details

Study Description

Brief Summary

There is a pandemic in the world by COVID-19. Currently, the pharmacological curative or prophylactic treatments for this infection are not known. Recent studies have suggested that Hydroxy-Chloroquine could be effective in vitro and in vivo against COVID-19. The main objective of this study is to assess in patients with autoimmune disease treated with long course Hydroxy-Chloroquine initiated before the pandemic COVID-19 had an independent protective effect on the risk or the severity of infection with COVID-19.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: COVID 19 serology
  • Other: COVID 19 Self-Questionnaire
N/A

Detailed Description

A pre- or post-exposure treatment strategy has been validated in some infectious diseases. In particular, in HIV infection, this type of prophylactic treatment reduces the rate of infection in at-risk populations. The first studies from Chinese show that in case of immunosuppression or immunosuppressive treatment, whatever the causal pathology, COVID-19 infection is more severe. The present study presents a population of patients with lupus (SLE) or Gougerot's disease (SGD) who are treated for a long time, with Hydroxy-Chloroquine. The protective effect against COVID-19 infection of Hydroxy-Chloroquine compared to populations not exposed to this drug requires to be assessed in patients and their control groups under or without immunosuppressive treatments.

It is hypothesized that long-term treatment with Hydroxy-Chloroquine in SLE or SGD taken in its usual indication before the onset of the pandemic could decrease the number of COVID19 infections and/or the intensity of the disease.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
800 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Real-life Evaluation of the Efficacy of Pre-exposure Treatment With Hydroxy-Chloroquine on the Risk and Severity of COVID-19 Infection in Patients Receiving Long-term Treatment for Systemic Lupus Erythematosus and/or Gougerot's Disease
Actual Study Start Date :
Sep 9, 2020
Anticipated Primary Completion Date :
Mar 1, 2022
Anticipated Study Completion Date :
Mar 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: Patient treated with Hydroxy-chloroquine

patients treated with Hydroxy-Chloroquine (HC) with or without immunosuppressants (IS)(HC+ group, n=400)

Diagnostic Test: COVID 19 serology
Diagnosis of Covid-19 past infection will be made by serology

Other: COVID 19 Self-Questionnaire
COVID 19 Self-Questionnaire

Other: Patient without treatment with Hydroxy-chloroquine

patients without treatment with Hydroxy-Chloroquine with or without immunosuppressants

Diagnostic Test: COVID 19 serology
Diagnosis of Covid-19 past infection will be made by serology

Other: COVID 19 Self-Questionnaire
COVID 19 Self-Questionnaire

Outcome Measures

Primary Outcome Measures

  1. Rate of patients with positive anti-COVID19 serology [Day 1]

    Rate of patients with positive anti-COVID19 serology with or without Hydroxy-Chloroquine.

Secondary Outcome Measures

  1. Rate of patients with symptomatic or severe (hospitalization) form of infection [Day 1]

    Rate of patients with symptomatic or severe (hospitalization) form of infection.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
Group with hydroxychloroquine treatment (HC +):
  • LED/SG diagnosed

  • Treatment with Hydroxy-Chloroquine in the 3 months before and during the outbreak at COVID 19, at least in December 2019. Patients may have treatment with immunosuppressants in combination with Hydroxy-Chloroquine.

  • COVID19 diagnostic questionnaire and available serology result.

Group without hydroxychloroquine treatment (HC-) :
  • No Hydroxy-Chloroquine intake for more than 12 months

--> HC- without an immunosuppressant

  • Viral hepatitis C cured for more than 12 months or primitive bile cholangitis (CBP) whose diagnosis is based on international criteria.

  • Non-significant liver fibrosis assessed either by historical histology or by fibroscan with non-significant liver fibrosis Metavir - F3 (at last available examination)

  • No Hydroxy-Chloroquine, or immunosuppressants have been taken for more than 12 months.

  • COVID19 diagnostic questionnaire and COVID19 serology result available.

-->HC- with an immunosuppressant

  • Diagnosis of LED/SG according to the CAB criteria revised in 1997 or autoimmune hepatitis according to the international criteria validated in 2008.

  • Patients treated with immunosuppressants for at least three months before the start of the pandemic at COVID 19, at least since December 2019.

  • COVID19 diagnostic questionnaire and available serology result.

Exclusion Criteria:
  • Anti-CD20 or Cyclophosphamide taken during the six months prior to the completion of the COVID 19 serology.

  • Refusal of a blood test for antibodies to COVID-19.

  • Protected adults

  • Pregnant or breastfeeding women.

  • Lack of health insurance coverage

Contacts and Locations

Locations

Site City State Country Postal Code
1 Limoges university Hospital Limoges France 87042
2 Montpellier University Hospital Montpellier France 31295
3 Pitié Salpêtrière Hospital - Hépatologie Paris France 75651
4 Pitié Salpêtrière Hospital - Médecine interne Paris France 75651
5 Haut-Lévêque Hospital - Gastro-entérologie Pessac France 33604
6 Haut-Lévêque Hospital - Médecine interne Pessac France 33604
7 Joseph Ducuing Hospital - Médecine interne Toulouse France 31027
8 Toulouse university Hospital - Larrey Dermatologie Toulouse France 31059
9 Toulouse University Hospital - Rhumatologie Toulouse France 31059
10 Toulouse University Hospital Toulouse France 31059
11 University Hospital of Toulouse - Rangueil Médecine interne Toulouse France 31059
12 University hospital Toulouse - Purpan Médecine interne Toulouse France 31059

Sponsors and Collaborators

  • University Hospital, Toulouse

Investigators

  • Principal Investigator: Laurent ALRIC, Pr, University Hospital, Toulouse

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University Hospital, Toulouse
ClinicalTrials.gov Identifier:
NCT04481633
Other Study ID Numbers:
  • RC31/20/0186
  • 2020-A01906-33
First Posted:
Jul 22, 2020
Last Update Posted:
Sep 8, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Toulouse
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 8, 2021