Epidemiology and Prevention of Congenital HCMV in Immune Mothers. Congenital HCMV Infection Lombardy (CHILd)
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|ClinicalTrials.gov Identifier: NCT03973359|
Recruitment Status : Recruiting
First Posted : June 4, 2019
Last Update Posted : June 4, 2019
Human cytomegalovirus (HCMV) is the leading infectious agent causing congenital disabilities such as mental retardation, psychomotor delay, hearing loss, speech and language disabilities, behavioural disorders and visual impairment. About 0.6% newborns are HCMV-congenitally infected and, among these, about 20% are symptomatic at birth or will develop long-term sequelae. The public health impact of congenital HCMV is substantial although greatly unrecognized. In Italy, estimated direct costs per affected child exceed €100.000 for a total of €60-70M. HCMV is also a significant cause of infection/disease in the immunocompromised host.
Epidemiological studies and population-based models have preliminarily documented that most of the burden associated to congenital HCMV would be due to non-primary maternal infection. Presently, reinfections are believed to be responsible for the great majority of infected fetuses born to immune mothers.
This study addresses incidence, outcome and prevention of congenital HCMV infection in seropositive pregnant women.The study includes 2 parts: part 1 in which the incidence and outcome of congenital HCMV is investigated in a large population of HCMV seropositive pregnant women and HCMV shedding and immune response is closely monitored in a subset of participants (nested study); part 2 in which the efficacy of an hygiene intervention is assessed.
|Condition or disease||Intervention/treatment||Phase|
|Congenital Cytomegalovirus Infection Maternal Cytomegalovirus Infection||Behavioral: Hygienic recommendations||Not Applicable|
Part 1. Epidemiologic study. To investigate incidence and outcome of congenital infection in immune mothers, clinical records of pregnant women are reviewed for HCMV serostatus at ≤ 13 weeks' gestation. Women with HCMV serology compatible with a remote infection are asked to participate in the study. Consenting women are given a pre-stamped, pre-addressed envelope containing a swab to collect newborn's saliva. Envelopes are sent by courier to a centralized diagnostic facility for HCMV testing.
Women can also be enrolled at delivery, provided that the woman has records of presence of virus-specific IgG and absence of IgM early during gestation(or in a previous pregnancy) or, in case of unknown serostatus, a sample of serum/plasma stored at ≤ 13 weeks' gestation is available for retrospective antibody testing (retrospective part of the epidemiology study).
Part 1. Nested study. A subset of IgG pos IgM neg women selected among those enrolled at ≤13 weeks' gestation in the epidemiology study are included in a nested study. These women are monitored at enrolment, 20, 30 weeks of gestation and at delivery by prospective determination of HCMV DNA excretion in different bodily fluids. In DNA-positive specimens selected HCMV genes will be sequenced.
Part 2. Prevention study. To assess the effectiveness of hygiene measures for prevention of congenital infection HCMV seropositive pregnant women are enrolled at ≤ 13 weeks' gestation. Part 2 starts when enrolment of Part 1 is completed. In practice, part 2 is a continuation of part 1 with the only addition of delivering hygiene information at enrolment.
Part 2 will not be performed in case congenital infection rate in Part 1 is <0.4% and clear maternal risk factor for intrauterine transmission cannot be identified at interim analysis (i.e. after examination of 5000 newborns).
In case HCMV DNA is detected in newborn's saliva, a urine sample is obtained for confirmation of congenital infection. Infants with documented congenital infection are clinically assessed at the time of diagnosis (for Part 1 and 2) and at one year of age (Part 1 only).
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||23500 participants|
|Intervention Model:||Sequential Assignment|
|Masking:||None (Open Label)|
|Official Title:||Incidence, Outcome and Prevention of Congenital Human Cytomegalovirus (HCMV) Infection in HCMV-seropositive Pregnant Women|
|Actual Study Start Date :||September 4, 2017|
|Estimated Primary Completion Date :||July 2020|
|Estimated Study Completion Date :||December 2020|
No Intervention: Epidemiology
HCMV-seropositive pregnant women receiving standard care
HCMV-seropositive pregnant women receiving hygienic information
Behavioral: Hygienic recommendations
Recommendation of protective behaviours such as frequent hand washing and avoiding risky behaviours such as kissing young children on the mouth or cheeks and sharing utensils, foods etc.
- Part 1. Epidemiology study. Incidence and clinical outcome of congenital HCMV infection in pregnant women with preconception immunity. [ Time Frame: Within 21 days of life ]Number of infants with ascertained congenital infection.
- Part 2. Prevention study. Efficacy of hygiene counseling in reducing congenital HCMV infection in pregnant women with preconception immunity. [ Time Frame: Within 21 days of life ]Number of infants with ascertained congenital infection born to HCMV seropositive women informed about hygiene measures compared to the number of newborns with congenital infection diagnosed in Part 1.
- Frequency of non-primary infections during pregnancy (Nested study) [ Time Frame: 10, 20, 30, 40 gestation weeks ]Number of participants with HCMV non-primary infection. HCMV non-primary infection is defined as detection of HCMV DNA shedding in bodily fluids.
- Frequency of HCMV re-infections vs re-activations during pregnancy (Nested study) [ Time Frame: 10, 20, 30, 40 gestation weeks ]Number of participants with HCMV re-infection or re-activation. Re-infection is defined as the appearance of genetically distinct HCMV strains; Reactivation is defined as the sustained presence of the same strain.
- Antigen-specific IgG levels in non-primary infection during pregnancy (Nested study) [ Time Frame: 10, 20, 30, 40 gestation weeks ]Levels of antigen-specific IgG in participants with or w/o non-primary infection.
- Antigen-specific IgM levels in non-primary infection during pregnancy (Nested study) [ Time Frame: 10, 20, 30, 40 gestation weeks ]Levels of antigen-specific IgM in participants with or w/o non-primary infection.
- Neutralizing antibody titers in non-primary infection during pregnancy (Nested study) [ Time Frame: 10, 20, 30, 40 gestation weeks ]Titers of neutralizing antibodies in participants with or w/o non-primary infection.
- Risk factors for congenital HCMV infection in pregnant women with preconception immunity. Age [ Time Frame: Delivery ]Age in mothers of newborns with or w/o congenital HCMV infection
- Risk factors for congenital HCMV infection in pregnant women with preconception immunity. Country of origin [ Time Frame: Delivery ]Country of origin of mothers of newborns with or w/o congenital HCMV infection
- Risk factors for congenital HCMV infection in pregnant women with preconception immunity. Occupation [ Time Frame: Delivery ]Occupation of mothers of newborns with or w/o congenital HCM infection
- Risk factors for congenital HCMV infection in pregnant women with preconception immunity. Contact with young children [ Time Frame: Delivery ]Contact with children <36 months in mothers of newborns with or w/o congenital HCMV infection
- Risk factors for congenital HCMV infection in pregnant women with preconception immunity. Twin pregnancy [ Time Frame: Delivery ]Twin vs singleton pregnancy in mothers of newborns with or w/o congenital HCMV infection
- Risk factors for congenital HCMV infection in pregnant women with preconception immunity. Concomitant pathologies [ Time Frame: Delivery ]Concomitant pathologies in mothers of newborns with or w/o congenital HCMV infection
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03973359
|Contact: Daniele Lilleri, MD||+39 0382 email@example.com|
|Contact: Gabriela Cassinelli, PhD||+39 0382 firstname.lastname@example.org|
|ASST Spedali Civili di Brescia||Recruiting|
|Brescia, Italy, 25123|
|Contact: Federico Prefumo, MD|
|Brescia, Italy, 25124|
|Contact: Giorgio Pagani, MD|
|ASST Vimercate (Ospedale di Carate Brianza)||Recruiting|
|Carate Brianza, Italy, 20841|
|Contact: Anna Locatelli, MD|
|ASST Monza (presidio di Desio)||Recruiting|
|Desio, Italy, 20832|
|Contact: Simona Rutolo, MD|
|Fondazione IRCCS Ospedale Maggiore Policlinico||Recruiting|
|Milan, Italy, 20122|
|Contact: Beatrice Tassis, MD|
|Ospedale Macedonio Melloni (ASST FBF-Sacco)||Recruiting|
|Milan, Italy, 20129|
|Contact: Michele Vignali, MD|
|Ospedale San Raffaele||Recruiting|
|Milan, Italy, 20132|
|Contact: Paolo Cavoretto, MD|
|Ospedale Buzzi (ASST FBF-Sacco)||Recruiting|
|Milan, Italy, 20154|
|Contact: Irene Cetin, MD|
|Ospedale Sacco (ASST FBF-Sacco)||Recruiting|
|Milan, Italy, 20157|
|Contact: Valeria Savasi, MD|
|Fondazione Monza Brianza per il Bambino e la sua Mamma||Recruiting|
|Monza, Italy, 20900|
|Contact: Patrizia Vergani, MD|
|Fondazione IRCCS Policlinico San Matteo||Recruiting|
|Contact: Arsenio Spinillo, MD|
|ASST dei Sette Laghi (Ospedale Filippo Del Ponte)||Active, not recruiting|
|Varese, Italy, 21100|
|Principal Investigator:||Daniele Lilleri, MD||Fondazione IRCCS Policlinico San Matteo|