Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

Effects of COVID 19 Vaccine on Egyptian Population

20. mars 2021 oppdatert av: Mariam Roshdy Elkhayat, Assiut University

Impact of COVID 19 Vaccine on Safety, Blood Elements, and Immunogenicity of the Egyptian Population

The aim of this study is to identify adverse events following vaccination by the COVID-19 vaccine by evaluating adverse side effects, hematological values; immunogenicity in the Egyptian candidates in response to COVID-19 vaccine, summarizing the which may occur following administration of COVID-19 vaccine.

Studieoversikt

Status

Ukjent

Intervensjon / Behandling

Detaljert beskrivelse

Coronavirus disease 2019 (COVID-19) is an emerging respiratory infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that had infected more than 100 million individuals and caused more than 2 million deaths worldwide by February 13, 2021. A safe and effective vaccination trials against COVID-19 is urgently needed. There are currently more than 160 COVID-19 candidate vaccines in development worldwide, and 25 are in different phases of clinical trials using different platforms.

The efficacy and immunogenicity of vaccines varies depending on the study cohort. Race and ethnicity were shown to affect the antibody responses to the rubella vaccine, which elicited significantly higher titers in children of African ethnicity compared to those of European descent or Hispanic ethnicity, likely, disparities in serologic responses to vaccines were also observed between different ethnic groups for the Haemophilus influenzae type b-tetanus toxoid conjugate vaccine , or the Haemophilus influenzae type b polysaccharide-Neisseria meningitidis outer membrane protein conjugate vaccine . thus keeping the race an important factor in studding its effect on immunogenicity of vaccine. Thus keeping the race an important factor in studding its effect on immunogenicity of vaccine, which pushed us to estimate immunogenicity in Egyptian population after vaccination with the inactivated COVID-19 vaccine.

Heamatological changes after vaccination had been detected in many researches; lecuocytosis was found shortly after vaccination of infants, which was primarily a neutrophilia but no participant received antibiotics and all remained well at follow-up . In a case series study, also leukocytosis with fever was detected following pneumococcal vaccine administration . On the other hand, neutropenia was detected following a new vaccine against Shigella sonnei . Platelets abnormalities also had been detected following vaccination, a previous example is idiopathic thrombocytopenic purpura, linked to the administration of measles-containing vaccines .

Studietype

Observasjonsmessig

Registrering (Forventet)

800

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 80 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

HCWs in Assiut University Hospitals accepted to take vaccine

Beskrivelse

Inclusion Criteria:

  1. People aged 18-80 years.
  2. Negative for serum-specific IgM/IgG antibodies against SARS-CoV-2, as measured by a commercial kit (Innovita, China) at the time of screening.

Exclusion Criteria:

  1. A history of infection with SARS-CoV 3 months before the vaccine.
  2. Fever, cough, runny nose, sore throat, diarrhoea, dyspnoea, or tachypnoea in the 14 days before vaccination.
  3. Pregnancy.
  4. A history of seizures or mental illness.
  5. Being on immunosuppressive agents.
  6. Being on anticoagulation therapy.
  7. Being unable to comply with the study schedule.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
serological antibodies against SARS-CoV-2 e
Tidsramme: change from baseline at one month after first dose
Total IgG titer
change from baseline at one month after first dose
serological antibodies against SARS-CoV-2 e
Tidsramme: one month after second dose
Total IgG titer
one month after second dose
Complete blood count (CBC)
Tidsramme: change from baseline at one month after first dose
to evaluate total leucocyte count TLC
change from baseline at one month after first dose
Complete blood count (CBC)
Tidsramme: one month after second dose
to evaluate total leucocyte count TLC
one month after second dose
Complete blood count (CBC)
Tidsramme: change from baseline at one month after first dose
absolute neutrophilic count (ANC)
change from baseline at one month after first dose
Complete blood count (CBC)
Tidsramme: one month after second dose
absolute neutrophilic count (ANC)
one month after second dose
Complete blood count (CBC)
Tidsramme: change from baseline at one month after first dose
platelets (PLTs)
change from baseline at one month after first dose
Complete blood count (CBC)
Tidsramme: one month after second dose
platelets (PLTs)
one month after second dose
Complete blood count (CBC)
Tidsramme: change from baseline at one month after first dose
hemoglobin level
change from baseline at one month after first dose
Complete blood count (CBC)
Tidsramme: one month after second dose
hemoglobin level
one month after second dose
Adverse clinical symptoms after vaccine
Tidsramme: up to one week after first dose

asking about possible recorded side effects as

  • Local: irritation, erythema, swelling, or itching.
  • Systemic: headache, dizziness, difficult sleep, flush, muscle pain, joint pain, fatigue, fever, chills, sore throat, nasal congestion, nasal bleeds, sneezing, runny nose, cough, dyspnoea, palpitation, nausea, vomiting, diarrhoea, constipation, stomach pain, loss of appetite, acute allergic reaction, acne, abnormal taste, loss of taste, mouth ulcers, toothache, ear pain, eye pain, and/or lymphadenopathy.
up to one week after first dose

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Forventet)

1. mars 2021

Primær fullføring (Forventet)

1. september 2021

Studiet fullført (Forventet)

30. desember 2021

Datoer for studieregistrering

Først innsendt

14. mars 2021

Først innsendt som oppfylte QC-kriteriene

19. mars 2021

Først lagt ut (Faktiske)

22. mars 2021

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

24. mars 2021

Siste oppdatering sendt inn som oppfylte QC-kriteriene

20. mars 2021

Sist bekreftet

1. mars 2021

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Kliniske studier på Covid-19-vaksine

Kliniske studier på viral vector vaccine

3
Abonnere