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N/A N=160

Cytomegalovirus Shedding Characteristics in Pregnant Women

CMV · Congenital Cmv · Maternal Infections Affecting Fetus or Newborn · Shedding Virus

Enrolled (actual)
160
Serious AEs
6.9%
Results posted
Jun 2024
Primary outcome: Primary: The Prevalence of CMV Shedding in Saliva, Urine and Vaginal Secretions of CMV Seropositive Women in Pregnancy — 27; 4; 16; 20 Participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
No intervention- not applicable (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
St George's, University of London
Primary completion
Oct 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
The Prevalence of CMV Shedding in Saliva, Urine and Vaginal Secretions of CMV Seropositive Women in Pregnancy
27; 4; 16; 20
SECONDARY
The Proportion of CMV Shedding in Saliva, Urine and Vaginal Secretions of CMV Seropositive Women Throughout Pregnancy and Postpartum
3; 9; 9; 3; 10; 10
SECONDARY
The Quantity of CMV Shedding in Saliva, Urine and Vaginal Secretions in CMV Seropositive Women Throughout Pregnancy and Postpartum
521.0; 1.0; 800.0; 693.0; 104.5; 189.5
SECONDARY
The Proportion of Pregnant Women Approached Who Are Recruited Into the Study
966; 804; 384; 160
SECONDARY
The Proportion of Participating Pregnant Women Completing the Study
66; 123; 119
SECONDARY
The Acceptability of the Study Procedures to Participating Pregnant Women
4.03; 4.57; 4.38; 4.48; 4.50; 4.22
SECONDARY
The Association of Demographics With CMV Shedding in CMV Seropositive Women in Pregnancy
3.17; 0.95; 1.02; 1.41; 0.99; 0.36
SECONDARY
The Association of Contact With Young Children's Bodily Fluids With CMV Shedding in CMV Seropositive Women Throughout Pregnancy and Postpartum
0; 0.74; 0.74; 0.99; 0.81; 1.10
SECONDARY
The Prevalence of CMV-specific T-cell Immune Responses as Measured by CMV-QuantiFERON in CMV Seropositive Women in Pregnancy
62
SECONDARY
The Prevalence of CMV-specific T-cell Immune Responses as Measured by CMV-ELISPOT in CMV Seropositive Women in Pregnancy
67
SECONDARY
The Proportion of CMV-specific T-cell Immune Responses as Measured by CMV-QuantiFERON in CMV Seropositive Women Throughout Pregnancy and Postpartum
50; 39; 31; 10
SECONDARY
The Proportion of CMV-specific T-cell Immune Responses as Measured by CMV-ELISPOT in CMV Seropositive Women Throughout Pregnancy and Postpartum
49; 24; 25; 8
SECONDARY
The Association Between CMV-specific T Cell Immune Response and CMV Shedding in CMV Seropositive Pregnant Women as Measured by CMV-QuantiFERON
0.56; 1.19; 2.82; 0.00
SECONDARY
The Association Between CMV-specific T Cell Immune Response and CMV Shedding in CMV Seropositive Pregnant Women as Measured by CMV-ELISPOT
1.00; 0.99; 1.00; 0.97; 1.00; 0.99

Summary

The cCHIPS study is a feasibility study for larger scale multi-centre studies and is designed as a single-centre observational cohort, longitudinal, natural history study. The overarching aim of this study is to evaluate the feasibility of performing larger scale, multi-centre studies to evaluate the relationship between CMV shedding in pregnancy with congenital CMV (cCMV). There is no randomisation involved in this study and all participants will perform the same study procedures and receive treatment as usual. The primary (main) objective is to evaluate the prevalence (percentage of occurrence) of CMV shedding in saliva, urine and vaginal secretions of CMV seropositive women throughout pregnancy. The secondary objectives are to evaluate the quantity of CMV shedding in saliva, urine and vaginal secretions of CMV seropositive women throughout pregnancy, to compare the prevalence and quantity of CMV shedding in CMV seropositive women between different sources of shedding (saliva, urine or vaginal secretions) and different gestational stages, to identify risk factors for CMV shedding in CMV seropositive pregnant women, to evaluate the acceptability of the study procedures to the participating pregnant women, to evaluate the proportion of women approached who are recruited into the study and who are completing the study, and to evaluate the relationship between CMV specific cell mediated immunity (a type of immune protection following exposure to CMV) and CMV shedding in CMV seropositive pregnant women. The tertiary objective is to compare the evaluation of CMV specific T cell immune responses (a type of CMV specific cell mediated immunity) between the two commercially available CMV-specific T cell immune response assays which are QuantiFERON-CMV and CMV-ELISPOT assays. This study will aim to recruit 200 pregnant women. This study will be undertaken in parallel with a separate study called RACE-FIT (REC reference number 18/SC/0360, IRAS ID 239977), which will have ethical approval to screen pregnant women with children less than 4 years of age booked for their antenatal care at St George's Hospital, London, identified during the antenatal combined screening bloods appointment or the antenatal booking appointment, for their CMV serology status on a sample of blood collected as part of the screening process. As part of the ethical approval sought for the RACE-FIT study and the cCHIPS study, the pregnant women screened and found to be CMV seronegative will be eligible for recruitment into the RACE-FIT study and those screened and found to be CMV seropositive will be eligible and approached for recruitment into the cCHIPS study. The cCHIPS study aim to recruit over a 6 month period. The study involves four visits (Visit 1, Visit 2, Visit 3, Visit 4) for each participant. The total study period for each participant will be between 6 to 8 months.

Eligibility Criteria

Inclusion Criteria

  • Pregnant
  • CMV seropositive
  • Willing and able to provide informed consent
  • Living with child(ren), at least one of whom is less than four years old
  • Willing to have saliva, urine and vaginal secretion sampling to be tested for CMV PCR
  • Willing to be followed up until the postpartum period

Exclusion Criteria

  • Age less than 18 years
  • Evidence of acute maternal CMV infection at the time of screening
  • Documented immunodeficiency of any aetiology including the use of oral steroid therapy equivalent to >1mg/kg of prednisone per day for more than one week
  • In the opinion of the investigator is unlikely to comply with the study procedures
  • In the opinion of the investigator does not have adequate understanding or verbal and written English
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04021628). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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