Hematologic DiseasesCYTOALLOSURVEYNCT04412811
Prospective Survey of CMV, Herpesviruses Infections and Diseases in Allo-HSCT
An observational study of Hematologic Diseases and Stem Cell Transplant Complications, run by Gruppo Italiano Trapianto di Midollo Osseo at 50 sites in Italy.
Trial summary
Prospective observational study of epidemiological surveillance, multicenter, non-profit, spontaneous, Italian with objective to describe the incidence of CMV infections and diseases in adult and pediatric patients undergoing allo-HSCT during the first 6 months from transplant. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Hematologic Diseases, Stem Cell Transplant Complications, Cytomegalovirus Viremia
- How many people
- 1,310 participants
- Where
- 50 sitesItaly
- Study dates
- 1 Jan 2021to 31 Mar 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Adult and children allogenic Hematopoietic stem cell transplantation recipients
Who may be able to join
- Prospective observational study of epidemiological surveillance, multicenter, non-profit, spontaneous, Italian with objective to describe the incidence of CMV infections and diseases in adult and pediatric patients undergoing allo-HSCT during the first 6 months from transplant. This study will evaluate approximately 1500 subjects, with competitive enrolment from GITMO investigational centers.
Who cannot join
- Absence of consent Written information
Trial locations and contacts
50 sites in 1 country.
50 sites in 1 country
Italy50 sites
Azienda Ospedaliero-Universitaria Ospedali Riuniti
Ancona
Ospedale Mazzoni
Ascoli Piceno
A.O.S. G. Moscati
Avellino
Policlinico di Bari-Ematologia con trapianti
Bari
Divisione di Ematologia - Ospedali Papa Giovanni XXIII
Bergamo
A.O.U. Policlinico S.Orsola-Malpighi
Bologna
Ospedale San Orsola
Bologna
Ospedale Regionale Generale- Divisione Ematologia
Bolzano
AO Spedali Civili di Brescia- USD - TMO Adulti
Brescia
Azienda Sanitaria Locale Br1 Ospedale "A. Perrino
Brindisi
CTMO PO "Businco" A.O. "G. Brotzu"
Cagliari
Ospedale Ferrarotto
Catania
Struttura Complessa di Ematologia, Azienda Ospedaliera Santa Croce e Carle
Cuneo
Azienda Ospedaliera di Careggi
Florence
Ematologia e Centro Trapianti Midollo Osseo - Ospedale IRCCS Casa Sollievo della Sofferenza
Foggia
AOU-IRCCS San Martino-IST
Genova
Ospedale Gaslini
Genova
Policlinico VIto Fazzi
Lecce
AOU Integrata
Mestre
Divisione di Ematologia - Istituto Nazionale dei Tumori
Milan
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
Milan
Ospedale San Raffaele
Milan
Divisione Ematologia - Azienda Ospedaliera Universitaria - Policlinico -
Modena
Ospedale San Gerardo
Monza
A.O.U. Policlinico Federico II
Naples, Napoli
AOU S. Giovanni di Dio e Ruggi D'Aragona
Naples
Uoc Sit Tmo
Naples
UOSC Ematologia con Trapianto CSE, AORN A. Cardarelli, AORN Cardarelli
Naples
Azienda Ospedaliera di Padova
Padova
CTMO Osp. V. Cervello Azienda Ospedaliera Ospedali Riuniti Villa Sofia Cervello
Palermo
Azienda ospedaliera Universitaria di Parma
Parma
Fondazione IRCCS San Matteo
Pavia, Pavia, 27100
Policlinico San Matteo
Pavia
Ospedale S. Maria della Misericordia
Perugia
Dip. di Ematologia - Unità di Terapia Intensiva Ematologica per il Trapianto Emopoietico - Ospedale Civile di Pescara
Pescara
Azienda Ospedaliero Universitaria Pisana
Pisa
Ospedale San Carlo
Potenza, Italy
Centro Unico Regionale Trapianti di Midollo Osseo - Ospedale Bianchi-Melacino-Morelli
Reggio Calabria
Arciospedale S. M. Novella
Reggio Emilia
Divisione di Ematologia - Istituto di Semeiotica Medica - Policlinico A. Gemelli
Roma
Ospedale Bambin Gesù
Roma
Policlinico Tor Vergata
Roma
Policlinico Umberto I
Roma
Dipartimento di Oncologia Medica ed Ematologia - Istituto Clinico Humanitas
Rozzano (MI)
Ospedale Moscati
Taranto
AOU CIttà della Salute e della Scienza
Torino
Ospedale Regina Margherita
Torino
UO Ematologia e TMO - Ospedale C. Panico
Tricase, Lecce
A.O. Santa Maria della Misericordia
Udine
Policlinico GB Rossi
Verona, Italy
About this study
Official title: A Prospective, Multicenter Survey of Cytomegalovirus (CMV) and Other Herpesviruses Infections and Diseases in Allogeneic Hematopoietic Stem Cell Transplant (allo-HSCT) Recipients.
Prospective observational study of epidemiological surveillance, multicenter, non-profit, spontaneous, Italian with objective to describe the incidence of CMV infections and diseases in adult and pediatric patients undergoing allo-HSCT during the first 6 months from transplant. This study will evaluate approximately 1500 subjects (with competitive enrolment) from GITMO investigational centers.
Read the detailed description
This is a prospective observational study of epidemiological surveillance, multicenter, non-profit, spontaneous, italian on patients submitted to allogeneic haematopoietic stem cell transplantation organized under the auspices of the Gruppo Italiano Trapianti di Midollo Osseo that involves the principal Centres active in transplantation of any kind of hematopoietic stem cells in Italy.
Allogeneic haematopoietic stem cell transplantation patients continue to be one of the highest risk categories for developing viral infections. Cytomegalovirus infection is the leading viral cause of morbidity and mortality and HHV6 and EBV are other major causes of complications in transplant. The risk of these infections is directly related to the type of transplant.
A better and continuous monitoring of Cytomegalovirus and other herpesviruses complication in this setting would contribute to a better knowledge of the evolving epidemiology and would lead to a better use of diagnostic strategies and of preventive and therapeutic measures.
This study is aimed to identify epidemiological characteristics of allogeneic haematopoietic stem cell transplantation patients developing cytomegalovirus and other herpesviruses infections, risk factors, diagnostic peculiarities and factors that may guide to pre-emptive therapy versus prophylaxis strategies.
Virological monitoring and health care resources utilization in Allogeneic haematopoietic stem cell transplantation recipients according to the different risk of viral infection will be also assessed. This prospective analysis will provide useful information for local clinicians to define tailored antiviral strategies in line with the change of transplantation procedures.
All consecutive patients submitted to allogeneic haematopoietic stem cell transplantation will be prospectively monitored for Cytomegalovirus Cytomegalovirus, Herpesvirus human 6 and Virus Epstein-Barr infections and diseases during the six months from transplant, because most of viral infections and diseases occur within this period after transplant. Risk factors, incidence and prognostic factors of each viral infection and disease, as well as diagnostic and therapeutic strategies employed in the various transplant centers, will be evaluated in the overall population and in subpopulations according to different transplant characteristics.
The incidence of these infections and diseases will be also collected and described according to the different types of transplant and underlying disease conditions.
The Secondary Objectives are:
To assess the factors that may affect the incidence and the prognosis of allogeneic haematopoietic stem cell transplantation infections and diseases, as well as of Herpesvirus human 6 and Virus Epstein-Barr infections and related diseases To assess the impact of allogeneic haematopoietic stem cell transplantation infections and diseases on the overall and attributable mortality at 12 months from the transplant To describe the virological diagnostic strategies of allogeneic haematopoietic stem cell transplantation, Herpesvirus human 6 and Virus Epstein-Barr infections and the allogeneic haematopoietic stem cell transplantation specific immunological reconstitution tests used in the various centres To describe the antiviral strategies employed in the various centers and in the various subpopulations of transplant patients with focus on use of antiviral drugs in prophylaxis and therapy and use of allogeneic haematopoietic stem cell transplantation -specific intravenous IVIG in prophylaxis and therapy To evaluate the impact of a local strategy about use of antiviral drugs and allogeneic haematopoietic stem cell transplantation -specific IVIG in prophylaxis and therapy on the epidemiological findings, the clinical evolution of the allogeneic haematopoietic stem cell transplantation infections and diseases and on the Health Care Resources utilization (diagnostic procedures, pharmaco-utilization, hospitalization, outpatient visits).
A web system data entry will be used for this study. Data will be stored using specific e-CRFs designed by GITMO committee and includes mainly descriptive variables. Data Center will perform extensive consistency checks and issue electronic Query Forms in case of inconsistent data. Follow-up period for the evaluation of survival will be from the date of transplant until 12 months post-transplant or death. However, patients may not have 12 months follow up and if the patients are not having 12 months of observation due to lost to follow up and not due to mortality, these patients characteristics will be compared with the rest of the patients in order to ascertain there is no bias or estimate the bias.
The study will be conducted according to the principles of Good Clinical Practice, the current Italian and European laws and regulations, in agreement with the declaration of Helsinki. The protocol has been written and the study will be conducted according to The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use Harmonized Tripartite Guideline for Good Clinical Practice, issued by the European Union. The responsible Local Ethical Committee approval must be obtained before starting the trial. A copy of the patient informed consent form must be submitted to the appropriate authority or committee, together with the protocol for written approval. Written approval of the protocol and informed consent by the responsible and appropriate authority or committee must be obtained prior to recruitment of patients to the study.
- Conditions
- Hematologic Diseases, Stem Cell Transplant Complications, Cytomegalovirus Viremia, Herpesvirus Infection
- Keywords
- Haematopoietic transplantation, CMV, Herpesviruses
- Medical subject headings
- Hematologic Diseases, Herpesviridae Infections
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Patients with hematological disease | Adult and children allogenic Hematopoietic stem cell transplantation recipients |
What is being measured
The primary outcome is the main question the study is designed to answer.
Cytomegalovirus infection
incidence of Cytomegalovirus after allogeneic haematopoietic stem cell transplantation
Measured: 6 months from transplant
Cytomegalovirus disease
incidence of Cytomegalovirus after allogeneic haematopoietic stem cell transplantation
Measured: 6 months from transplant
Herpesvirus human 6 infection
incidence of human 6 infection after allogeneic haematopoietic stem cell transplantation
Measured: 6 months from transplant
Herpesvirus human 6 disease
incidence of human 6 disease after allogeneic haematopoietic stem cell transplantation
Measured: 6 months from transplant
Virus Epstein-Barr infection
incidence of Virus Epstein-Barr infections after allogeneic haematopoietic stem cell transplantation
Measured: 6 months from transplant
Virus Epstein-Barr disease
incidence of Virus Epstein-Barr disease after allogeneic haematopoietic stem cell transplantation
Measured: 6 months from transplant
Secondary outcomes (6)
Overall Survival (OS)
OS is defined as the time from transplant to the date of death due to any cause or to the last date the patient was known to be alive (censored observation) or to the date of the data cut-off for final analysis
Measured: These outcome measures will be assessed at 1 year from transplant
Disease Free Survival (DFS)
DFS is defined as the probability of being alive free of disease at any point in time.
Measured: These outcome measures will be assessed at 1 year from transplant
Transplant Related Mortality (TRM)
TRM was defined as death due to any transplantation-related cause other than disease
Measured: These outcome measures will be assessed at 1 year from transplant
Relapse risk (RR)
RR or risk ratio is the ratio of the probability of an outcome in an exposed group to the probability of an outcome in an unexposed group.
Measured: These outcome measures will be assessed at 1 year from transplant
Acute Graft-versus-Host Disease
cumulative incidence of acute GvHD (grade II-IV)
Measured: These outcome measures will be assessed at 100 days from transplant
chronic graft-versus-host disease
cumulative incidence and severity of chronic graft-versus-host disease
Measured: These outcome measures will be assessed at 1 year from transplant
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Jun 2020
- Study start1 Jan 2021
- Primary completion31 Jul 2022
- Study completion31 Mar 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Hematologic DiseasesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1,310 participants (actual)
Sponsor and investigators
- Lead sponsor
- Gruppo Italiano Trapianto di Midollo Osseo
- Sponsor type
- University, hospital or other
- Collaborators
- Azienda Policlinico Umberto I
- Responsible party
- Sponsor
- Investigators
- Corrado Girmenia, Principal investigator, Azienda Policlinico Umberto I
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04412811
- Sponsor's protocol ID
- CYTOALLO GITMO-AMCLI SURVEY
- Acronym
- CYTOALLOSURVEY
- Status last verified
- Jan 2025
- First submitted
- 29 May 2020
- Last updated
- 6 Jan 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Girmenia C, Chiusolo P, Marsili G, Piciocchi A, Mico MC, Greco R, Porto G, Galaverna F, Bonifazi F, Cutini I, Malagola M, Bramanti S, Busca A, Carella AM, Carotti A, Iori AP, Onida F, Bono R, Terruzzi E, Vacca A, Rinaldi A, Cavattoni IM, Picardi A, Faraci M, Lazzarotto T, Baldanti F, Clerici P, Castagna L, Martino M, Ciceri F. The Changing Impact of Human Cytomegalovirus Serology and Infection on Patient Outcome After Allogeneic Hematopoietic Stem Cell Transplantation: An Italian Prospective Multicenter Survey in the Era of Letermovir Prophylaxis. Open Forum Infect Dis. 2025 Apr 18;12(5):ofaf233. doi: 10.1093/ofid/ofaf233. eCollection 2025 May.
PubMed 40322267
Study at a glance
From the registry record, last updated by the sponsor on 6 Jan 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Prospective, Multicenter Survey of Cytomegalovirus (CMV) and Other Herpesviruses Infections and Diseases in Allogeneic Hematopoietic Stem Cell Transplant (allo-HSCT) Recipients.
- ClinicalTrials.gov ID
- NCT04412811
- Acronym / sponsor ID
- CYTOALLOSURVEY / CYTOALLO GITMO-AMCLI SURVEY
- Conditions
- Hematologic Diseases, Stem Cell Transplant Complications, Cytomegalovirus Viremia, Herpesvirus Infection
- Keywords
- Haematopoietic transplantation, CMV, Herpesviruses
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 1,310 participants (actual)
- Lead sponsor
- Gruppo Italiano Trapianto di Midollo OsseoUniversity, hospital or other
- Collaborators
- Azienda Policlinico Umberto I
- Study start
- 1 Jan 2021 (actual)
- Primary completion
- 31 Jul 2022 (actual)
- Study completion
- 31 Mar 2023 (actual)
- First posted
- 2 Jun 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Prospective observational study of epidemiological surveillance, multicenter, non-profit, spontaneous, Italian with objective to describe the incidence of CMV infections and diseases in adult and pediatric patients undergoing allo-HSCT during the first 6 months from transplant. This study will evaluate approximately 1500 subjects (with competitive enrolment) from GITMO investigational centers.
Detailed description
This is a prospective observational study of epidemiological surveillance, multicenter, non-profit, spontaneous, italian on patients submitted to allogeneic haematopoietic stem cell transplantation organized under the auspices of the Gruppo Italiano Trapianti di Midollo Osseo that involves the principal Centres active in transplantation of any kind of hematopoietic stem cells in Italy.
Allogeneic haematopoietic stem cell transplantation patients continue to be one of the highest risk categories for developing viral infections. Cytomegalovirus infection is the leading viral cause of morbidity and mortality and HHV6 and EBV are other major causes of complications in transplant. The risk of these infections is directly related to the type of transplant.
A better and continuous monitoring of Cytomegalovirus and other herpesviruses complication in this setting would contribute to a better knowledge of the evolving epidemiology and would lead to a better use of diagnostic strategies and of preventive and therapeutic measures.
This study is aimed to identify epidemiological characteristics of allogeneic haematopoietic stem cell transplantation patients developing cytomegalovirus and other herpesviruses infections, risk factors, diagnostic peculiarities and factors that may guide to pre-emptive therapy versus prophylaxis strategies.
Virological monitoring and health care resources utilization in Allogeneic haematopoietic stem cell transplantation recipients according to the different risk of viral infection will be also assessed. This prospective analysis will provide useful information for local clinicians to define tailored antiviral strategies in line with the change of transplantation procedures.
All consecutive patients submitted to allogeneic haematopoietic stem cell transplantation will be prospectively monitored for Cytomegalovirus Cytomegalovirus, Herpesvirus human 6 and Virus Epstein-Barr infections and diseases during the six months from transplant, because most of viral infections and diseases occur within this period after transplant. Risk factors, incidence and prognostic factors of each viral infection and disease, as well as diagnostic and therapeutic strategies employed in the various transplant centers, will be evaluated in the overall population and in subpopulations according to different transplant characteristics.
The incidence of these infections and diseases will be also collected and described according to the different types of transplant and underlying disease conditions.
The Secondary Objectives are:
To assess the factors that may affect the incidence and the prognosis of allogeneic haematopoietic stem cell transplantation infections and diseases, as well as of Herpesvirus human 6 and Virus Epstein-Barr infections and related diseases To assess the impact of allogeneic haematopoietic stem cell transplantation infections and diseases on the overall and attributable mortality at 12 months from the transplant To describe the virological diagnostic strategies of allogeneic haematopoietic stem cell transplantation, Herpesvirus human 6 and Virus Epstein-Barr infections and the allogeneic haematopoietic stem cell transplantation specific immunological reconstitution tests used in the various centres To describe the antiviral strategies employed in the various centers and in the various subpopulations of transplant patients with focus on use of antiviral drugs in prophylaxis and therapy and use of allogeneic haematopoietic stem cell transplantation -specific intravenous IVIG in prophylaxis and therapy To evaluate the impact of a local strategy about use of antiviral drugs and allogeneic haematopoietic stem cell transplantation -specific IVIG in prophylaxis and therapy on the epidemiological findings, the clinical evolution of the allogeneic haematopoietic stem cell transplantation infections and diseases and on the Health Care Resources utilization (diagnostic procedures, pharmaco-utilization, hospitalization, outpatient visits).
A web system data entry will be used for this study. Data will be stored using specific e-CRFs designed by GITMO committee and includes mainly descriptive variables. Data Center will perform extensive consistency checks and issue electronic Query Forms in case of inconsistent data. Follow-up period for the evaluation of survival will be from the date of transplant until 12 months post-transplant or death. However, patients may not have 12 months follow up and if the patients are not having 12 months of observation due to lost to follow up and not due to mortality, these patients characteristics will be compared with the rest of the patients in order to ascertain there is no bias or estimate the bias.
The study will be conducted according to the principles of Good Clinical Practice, the current Italian and European laws and regulations, in agreement with the declaration of Helsinki. The protocol has been written and the study will be conducted according to The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use Harmonized Tripartite Guideline for Good Clinical Practice, issued by the European Union. The responsible Local Ethical Committee approval must be obtained before starting the trial. A copy of the patient informed consent form must be submitted to the appropriate authority or committee, together with the protocol for written approval. Written approval of the protocol and informed consent by the responsible and appropriate authority or committee must be obtained prior to recruitment of patients to the study.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patients with hematological disease | – | –Adult and children allogenic Hematopoietic stem cell transplantation recipients |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Adult and children allogenic Hematopoietic stem cell transplantation recipients
Key inclusion criteria (1 listed)
- Prospective observational study of epidemiological surveillance, multicenter, non-profit, spontaneous, Italian with objective to describe the incidence of CMV infections and diseases in adult and pediatric patients undergoing allo-HSCT during the first 6 months from transplant. This study will evaluate approximately 1500 subjects, with competitive enrolment from GITMO investigational centers.
Key exclusion criteria (1 listed)
- Absence of consent Written information
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Cytomegalovirus infection
Time frame: 6 months from transplant
incidence of Cytomegalovirus after allogeneic haematopoietic stem cell transplantation
Cytomegalovirus disease
Time frame: 6 months from transplant
incidence of Cytomegalovirus after allogeneic haematopoietic stem cell transplantation
Herpesvirus human 6 infection
Time frame: 6 months from transplant
incidence of human 6 infection after allogeneic haematopoietic stem cell transplantation
Herpesvirus human 6 disease
Time frame: 6 months from transplant
incidence of human 6 disease after allogeneic haematopoietic stem cell transplantation
Virus Epstein-Barr infection
Time frame: 6 months from transplant
incidence of Virus Epstein-Barr infections after allogeneic haematopoietic stem cell transplantation
Virus Epstein-Barr disease
Time frame: 6 months from transplant
incidence of Virus Epstein-Barr disease after allogeneic haematopoietic stem cell transplantation
6 secondary outcomes
Overall Survival (OS)
Time frame: These outcome measures will be assessed at 1 year from transplant
Disease Free Survival (DFS)
Time frame: These outcome measures will be assessed at 1 year from transplant
Transplant Related Mortality (TRM)
Time frame: These outcome measures will be assessed at 1 year from transplant
Relapse risk (RR)
Time frame: These outcome measures will be assessed at 1 year from transplant
Acute Graft-versus-Host Disease
Time frame: These outcome measures will be assessed at 100 days from transplant
chronic graft-versus-host disease
Time frame: These outcome measures will be assessed at 1 year from transplant
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Jan 2025.
- Derived from this study: PubMed 40322267Girmenia C, Chiusolo P, Marsili G, Piciocchi A, Mico MC, Greco R, Porto G, Galaverna F, Bonifazi F, Cutini I, Malagola M, Bramanti S, Busca A, Carella AM, Carotti A, Iori AP, Onida F, Bono R, Terruzzi E, Vacca A, Rinaldi A, Cavattoni IM, Picardi A, Faraci M, Lazzarotto T, Baldanti F, Clerici P, Castagna L, Martino M, Ciceri F. The Changing Impact of Human Cytomegalovirus Serology and Infection on Patient Outcome After Allogeneic Hematopoietic Stem Cell Transplantation: An Italian Prospective Multicenter Survey in the Era of Letermovir Prophylaxis. Open Forum Infect Dis. 2025 Apr 18;12(5):ofaf233. doi: 10.1093/ofid/ofaf233. eCollection 2025 May.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Corrado Girmenia principal investigator
Azienda Policlinico Umberto I
50 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Hematologic Diseases and Stem Cell Transplant Complications, run by Gruppo Italiano Trapianto di Midollo Osseo at 50 sites in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 6 Jan 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 50 sites in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Cytomegalovirus infection (time frame: 6 months from transplant). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04412811, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Jan 2025.