Ganciclovir Resistant/Refractory Cytomegalovirus Infection in SOT Recipients and HSCT Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna

About this trial

The ReCySOHT study is a multicenter, retrospective, observational case-control study on the risk factors for developing a ganciclovir-resistant/refractory (GCV-RR) cytomegalovirus infection in patients receiving solid organ transplant (SOT) or hematopoietic stem cell transplant (HSCT). Aims of the study are to investigate the incidence of and risk factors for GCV-RR CMV infection in SOT recipients and HSCT patients in order to design further studies aimed at preventing and improving the patient management of GCV-RR CMV infections.

Eligibility criteria

Qualifiers

All adult (≥ 18 years) patients who underwent SOT or HSCT developing CMV-infection treated with GC/VGC

Ability to understand the purpose of the study and provide signed and dated informed consent

Disqualifiers

Lack of clinical and/or laboratory data regarding the type of CMV event

Lack of the serological mismatch at transplantation

Lack of the type of SOT or HSCT

Lack of the patient and graft outcome at 30, 60 or 90 days after CMV event diagnosis

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

100 Participants
are grouped into 1 trial group