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Pregnant and Lactating Individuals & Newborns COVID-19 Vaccination Prospective Cohort Study

Pregnancy Related | Vaccine Reaction | Immunogenicity | Covid19 | SARS-CoV2 Infection

The PLAN-V Study is an Ontario-based prospective, longitudinal study that will consist of extensive biosampling and detailed data collection from pregnant women/individuals, who have received the COVID-19 vaccine during their pregnancy, and their infants across the antenatal, delivery and postpartum periods.

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Conditions de participation

  • Sexe:

    FEMALE
  • Âges admissibles:

    0 and up

Critères de participation

Inclusion Criteria:

* Women/Individuals ≥ 16 years of age who are ≥7 0/7 weeks' gestation on the day of enrollment
* Capacity to provide informed consent and to comprehend and comply with the study requirements
* Planning to deliver at a participating site hospital
* Planning to receive or have previously received one-dose of a Health Canada approved COVID-19 vaccine (any product, any number of doses) during the current pregnancy

Exclusion Criteria:

* Cases with known major fetal concerns
* Women/Individuals who are fully vaccinated against COVID-19
* Women/Individuals who are pregnant due to surrogacy, or planning to give their child up for adoption
* Women/Individuals with a non-viable pregnancy (e.g., ectopic)

Lieu de l'étude

Hamilton Health Sciences Corporation
Hamilton Health Sciences Corporation
Hamilton, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Sarah McDonald, MD

[email protected]
Backup Contact

L. MacDonald

[email protected]
The Ottawa Hospital - Civic Campus
The Ottawa Hospital - Civic Campus
Ottawa, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Stephanie Boyd, MBA

[email protected]
613-737-8899
Backup Contact

Alysha Harvey, MSc

[email protected]
613-737-8899
The Ottawa Hospital - General
The Ottawa Hospital - General
Ottawa, Ontario
Canada

Contactez l'équipe d'étude

Backup Contact

Alysha Harvey, MSc

[email protected]
613-737-8899
Primary Contact

Stephanie Boyd, MBA

[email protected]
613-737-8899
Kingston Health Sciences Centre
Kingston Health Sciences Centre
Kingston, Ontario
Canada

Contactez l'équipe d'étude

Backup Contact

Jessica Pudwell, MSc, MPH

[email protected]
Primary Contact

Laura Gaudet, MD

[email protected]
Sunnybrook Health Sciences Centre
Sunnybrook Health Sciences Centre
Toronto, Ontario
Canada

Contactez l'équipe d'étude

Backup Contact

Susan O'Rinn

[email protected]
Primary Contact

Amir Aviram, MD

[email protected]
London Health Sciences
London Health Sciences
London, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Barbra deVrijer, MD

[email protected]
Backup Contact

Jennifer Ryder

[email protected]
St. Michael's Hospital
St. Michael's Hospital
Toronto, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Howard Berger, MD

[email protected]
Backup Contact

Arifa Rahman, M.B.B.S, MPH

[email protected]
Étude parrainée par
Ottawa Hospital Research Institute
Participants recherchés
Plus d'informations
ID de l'étude: NCT05115617