Epidemiology and Prevention of Congenital HCMV in Immune Mothers. Congenital HCMV Infection Lombardy

Congenital Cytomegalovirus Infection Clinical Trial

— CHILd  

Official title:

Incidence, Outcome and Prevention of Congenital Human Cytomegalovirus (HCMV) Infection in HCMV-seropositive Pregnant Women

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03973359
• Other study ID #: 20170011101
• Status: Recruiting
• Phase: N/A
• Start date: September 4, 2017
• Est. completion date: December 2020

Study information

• Verified date: May 2019
• Source: Foundation IRCCS San Matteo Hospital
• Contact: Daniele Lilleri, MD
• Phone: +39 0382 501501
• Email: d.lilleri[@]smatteo.pv.it
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 23500
• Est. completion date: December 2020
• Est. primary completion date: July 2020
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Adult (= 18 years old) pregnant women at =13 weeks gestation

• Presence of HCMV IgG and absence of IgM or presence of high avidity IgG with or without IgM

• Presence of HCMV-specific IgG and absence of IgM or presence of high avidity IgG in case of positive IgM at =13 weeks gestation documented by medical report or by retrospective antibody determination on samples stored at =13 weeks (for women enrolled at delivery)

• Willingness to participate in the study

• Ability to understand information material

• Written informed consent

Exclusion Criteria:

• Unreliable women as judged by the investigator

• Women not willing to give written consent

Related Conditions & MeSH terms

• Communicable Diseases
• Congenital Cytomegalovirus Infection
• Cytomegalovirus Infections
• Infection
• Maternal Cytomegalovirus Infection

Intervention

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.

Locations

Country	Name	City	State
Italy	ASST Spedali Civili di Brescia	Brescia
Italy	Poliambulanza Brescia	Brescia
Italy	ASST Vimercate (Ospedale di Carate Brianza)	Carate Brianza
Italy	ASST Monza (presidio di Desio)	Desio
Italy	Fondazione IRCCS Ospedale Maggiore Policlinico	Milan
Italy	Ospedale Buzzi (ASST FBF-Sacco)	Milan
Italy	Ospedale Macedonio Melloni (ASST FBF-Sacco)	Milan
Italy	Ospedale Sacco (ASST FBF-Sacco)	Milan
Italy	Ospedale San Raffaele	Milan
Italy	Fondazione Monza Brianza per il Bambino e la sua Mamma	Monza
Italy	Fondazione IRCCS Policlinico San Matteo	Pavia
Italy	ASST dei Sette Laghi (Ospedale Filippo Del Ponte)	Varese

Sponsors (2)

Lead Sponsor	Collaborator
Foundation IRCCS San Matteo Hospital	Fondazione Regionale per la Ricerca Biomedica (FRRB) - Regione Lombardia

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Part 1. Epidemiology study. Incidence and clinical outcome of congenital HCMV infection in pregnant women with preconception immunity.	Number of infants with ascertained congenital infection.	Within 21 days of life
Primary	Part 2. Prevention study. Efficacy of hygiene counseling in reducing congenital HCMV infection in pregnant women with preconception immunity.	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.	Within 21 days of life
Secondary	Frequency of non-primary infections during pregnancy (Nested study)	Number of participants with HCMV non-primary infection. HCMV non-primary infection is defined as detection of HCMV DNA shedding in bodily fluids.	10, 20, 30, 40 gestation weeks
Secondary	Frequency of HCMV re-infections vs re-activations during pregnancy (Nested study)	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.	10, 20, 30, 40 gestation weeks
Secondary	Antigen-specific IgG levels in non-primary infection during pregnancy (Nested study)	Levels of antigen-specific IgG in participants with or w/o non-primary infection.	10, 20, 30, 40 gestation weeks
Secondary	Antigen-specific IgM levels in non-primary infection during pregnancy (Nested study)	Levels of antigen-specific IgM in participants with or w/o non-primary infection.	10, 20, 30, 40 gestation weeks
Secondary	Neutralizing antibody titers in non-primary infection during pregnancy (Nested study)	Titers of neutralizing antibodies in participants with or w/o non-primary infection.	10, 20, 30, 40 gestation weeks
Secondary	Risk factors for congenital HCMV infection in pregnant women with preconception immunity. Age	Age in mothers of newborns with or w/o congenital HCMV infection	Delivery
Secondary	Risk factors for congenital HCMV infection in pregnant women with preconception immunity. Country of origin	Country of origin of mothers of newborns with or w/o congenital HCMV infection	Delivery
Secondary	Risk factors for congenital HCMV infection in pregnant women with preconception immunity. Occupation	Occupation of mothers of newborns with or w/o congenital HCM infection	Delivery
Secondary	Risk factors for congenital HCMV infection in pregnant women with preconception immunity. Contact with young children	Contact with children <36 months in mothers of newborns with or w/o congenital HCMV infection	Delivery
Secondary	Risk factors for congenital HCMV infection in pregnant women with preconception immunity. Twin pregnancy	Twin vs singleton pregnancy in mothers of newborns with or w/o congenital HCMV infection	Delivery
Secondary	Risk factors for congenital HCMV infection in pregnant women with preconception immunity. Concomitant pathologies	Concomitant pathologies in mothers of newborns with or w/o congenital HCMV infection	Delivery