Marchand, A. http://orcid.org/0000-0003-1858-8159
Caille, A.
Gissot, V.
Giraudeau, B.
Lengelle, C.
Bourgoin, H.
Largeau, B.
Leducq, S.
Maruani, A.
Funding for this research was provided by:
centre hospitalier régional universitaire de Tours (Appel d'Offre Interne 2018 - DR190041-TOPGUN)
Article History
Received: 10 May 2021
Accepted: 28 April 2022
First Online: 8 July 2022
Declarations
:
: This protocol has been granted both ANSM (French Regulatory Authority) and CPP (<i>Comité de Protection des Personnes</i>, French Ethical Review Committee) approval (19.03.28.46025). French law does not require local ethics committee approval for each participating center.The patient will be orally informed of the aim of the protocol and its procedures. Patients will also receive a written information document. The written and informed consent of the patient, if obtained, must be dated and signed both by the patient (or their parent or legal representatives) and the investigator before any further study intervention. Children ≥ 16 years old’s consent will also be sought.
: We will obtain patient’s (or their parents’ or legal representatives’ if under 18) consent for publication of the dataset and clinical photographs on trial enrollment. Children ≥ 16 years old’s consent will also be sought.
: The authors declare that they have no competing interests.