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Immunological Follow-up After SARS CoV2 Vaccination in Kidney Transplant Recipients (COVATRHUS)

U

University Hospital, Strasbourg, France

Status

Terminated

Conditions

Kidney Transplant Recipients

Treatments

Other: Study of the synthesis of antibodies directed against SARS

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The investigators goal is to assess the vaccine response of kidney transplant patients following vaccination against SARS-CoV-2.

The study population will be derived from cohorts of kidney transplant patients who have been transplanted for more than 3 months and have no contraindications to vaccination. These patients will be vaccinated as part of routine care with a CoV-2 SARS vaccine licensed in France.

In this cohort, the investigators wish to study the post-vaccination humoral response by assaying neutralizing antibodies against SARS CoV-2 and the specific cellular response of SARS Cov-2 by quantiferon and in vitro lymphocyte stimulation assays.

Enrollment

37 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male or female, 18 years of age or older
  • Patient vaccinated against SARS-CoV-2 as part of routine care
  • Kidney or pancreatic kidney transplant
  • Transplantation for more than 3 months
  • Subject affiliated to a social protection health insurance
  • Subject able to understand the objectives and risks of the research and to give signed and dated informed consent

Exclusion criteria

  • History of anaphylactic shock or known allergy to PEG
  • Known history of COVID or positive Covid serology in the 3 months prior to vaccination
  • Contraindication to an intramuscular injection
  • Impossibility to give informed information about the subject (subject in an emergency situation, difficulties in understanding the subject, ...)
  • Subject under safeguard of justice
  • Subject under guardianship

Trial contacts and locations

1

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Central trial contact

Sophie Caillard, MD

Data sourced from clinicaltrials.gov

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