KTD-innov
  • L'étude
  • Partenaires
  • FAQ patients
  • Actualités
  • Presse
  • Contact
  • Research
  • Partners
  • Patient's FAQ
  • News
  • Press room
  • Contact us

Patient's FAQ

Send your questions
Photo

KIDNEY TRANSPLANT AND RESEARCH​

  • ​Why should kidney transplant research be funded?​
Photo

Participation to the study

  • ​Does the study involve data from kidney donors or recipients?
  • How is data collected from the recipient?
  • Are there any selection criteria among patients?
  • Do we need the patient's consent to collect his data?
  • How long will the patient be involved in the study?
Photo

Why should kidney transplant research be funded?​​

​More than 1,500,000 people worldwide now live with kidney transplants, and there are thousands of failed transplants every year. Graft rejection is still a constant threat to patients. The consequences are immediate in terms of mortality and morbidity. Current research would reduce the number of rejections through more personalized monitoring and treatment.
Photo

How is data collected from the recipient?

Recipient data are collected in two ways. The first type of data concerns the patient's medical history and the medical data collected during the follow-up (blood and urine tests, histopathology of the biopsy, etc.). The second type of data concerns the evaluation of biomarkers of rejection in samples taken specifically for the study: blood proteins and RNA, urinary proteins and biopsy RNA.
Photo

Do we need the patient's consent to collect his/HER data?

Yes, in order for physicians to collect blood or urine samples for research purposes, they must have the prior consent of patients. They must sign a consent form for the biocollection and proposed research.
Photo

Does the study involve data from kidney donors or recipients?

Both. Some data are from the donor and others from the recipient.
Photo

Are there any selection criteria among patients?

No, there is no selection of patients to participate in the study. Patients are adults who have had a kidney transplant. These data are collected at the Nantes University Hospital, the Montpellier University Hospital, the Saint-Louis Hospital and the Necker Hospital in Paris, the Lyon Civil Hospital, the Bordeaux University Hospital and the Toulouse University Hospital.
Photo

How long will the patient be involved in the study?

Patient follow-up in the KTD-innov study begins on the day of transplantation and data/samples are collected during the year following transplantation.

    Send your questions

Send
Photo

Plan du site

L'étude
Partenaires
FAQ des patients
Actualités
​
Espace presse
Contact
Mentions légales

Contact

Hôpital Européen Georges Pompidou
56, rue Leblanc
75908 Paris Cedex 15
contact@ktdinnov.fr
Tel. +33 1 53 98 80 00

SOUSCRIRE à notre newsletter


Vous souhaitez recevoir les actualités de KTD-innov par :

Vous pouvez vous désabonner à tout moment en cliquant sur le lien dans le bas de page de nos e-mails. En vous abonnant, vos informations seront transférées à Mailchimp. Voir les pratiques de Mailchimp en matière de confidentialité.

Site map

Research
Partners
Patient's FAQ
News
Press room
Contact us
Legal notice

Contact

​Hôpital Européen Georges Pompidou
56, rue Leblanc
75908 Paris Cedex 15
contact@ktdinnov.fr
Tel. +33 1 53 98 80 00

Subscribe to the Newsletter


You wish to receive KTD-innov newsletter by:

You can unsubscribe at any time by clicking on the link at the bottom of our emails. By subscribing, your information will be transferred to Mailchimp. See Mailchimp's privacy practices.


2022 © Copyright - Labs Explorer pour l'Inserm
  • L'étude
  • Partenaires
  • FAQ patients
  • Actualités
  • Presse
  • Contact
  • Research
  • Partners
  • Patient's FAQ
  • News
  • Press room
  • Contact us