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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04445610
Other study ID # FMASU P31a/ 2020
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date July 1, 2020
Est. completion date November 1, 2020

Study information

Verified date June 2020
Source Ain Shams University
Contact Amira Al Balakosy, MD
Phone 01221977455
Email drbalakosy@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The following two mechanisms that explain the ability of measles vaccine to cause partial protection against COVID-19. The first is that measles vaccine may increase the ability of the immune system to fight off pathogens other than measles due to the generated bystander immunity that would enhance the overall immunity against the new coronavirus. The second is that SARS-CoV-2 is proven to have structure similarities with measles, which may cause cross-reactivity and immunity between measles vaccines and COVID-19, leading to partial protection against COVID-19 in vaccinated subjects


Description:

Objectives:

1. To identify Measles IgG titre in SARS-COV2 infected patients .

2. correlate level of Measles IgG titre with the clinical severity of COVID-19 disease.

Secondary Objective To find an association of the postulated protective role of measles vaccine and SARS-COV2 infection

Criteria:

Inclusion criteria:included patients would be divided into 3 groups according to clinical severity of COVID-19 disease (mild ,moderate & severe)

- All patients with confirmed COVID 19 confirmed by positive PCR . .

- Any age or gender.

Exclusion criteria:

- Any patient refusing to be involved in the study.

Methods:

- Informed consent will be taken from each subject

- Full clinical examination.

- Evaluation of Measles Antibody Titer:

The measles virus IgG antibody titer will be determined quantitatively by ELISA for quantitative determination of IgG class antibodies against Measles virus in human serum or plasma (citrate, heparin).

- Anonymous data will be retrieved from the admitted patients' files, such as:

- CBC, CRP, AST, ALT, ESR, Serum ferritin & SARS CoV 2 RNA PCR swab results.

- Chest X ray and/or CT chest.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date November 1, 2020
Est. primary completion date September 1, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- All patients with confirmed COVID 19.

- Any age or gender

Exclusion Criteria:

- - Any patient refusing to be involved in the study

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Egypt Faculty of Medicine Ain Shams University Research Institute- Clinical Research Center Cairo Non-US

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Viral clearance Achievement of two consecutive negative PCR results for COVID 19 and discharge from hospital 6 months