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NCT05234723

Ganciclovir Resistant Cytomegalovirus Infection in SOT Recipients.

Status unknown Last updated 10 February 2022
What this trial tests

trial in Cytomegalovirus Infections in 100 participants. Status unknown.

Timeline
1 February 2022
Primary endpoint
31 May 2022
30 June 2022

Quick facts

Lead sponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment100
Start date1 February 2022
Primary completion31 May 2022
Estimated completion30 June 2022

Conditions studied

Sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna — full company profile →

Who can join

18 and older, any sex, with Cytomegalovirus Infections. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Cytomegalovirus Infections

Currently open trials in the same condition.

Other IRCCS Azienda Ospedaliero-Universitaria di Bologna trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05234723.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing