ClinicalTrials.gg
RecruitingNCT05429346PCORISMMUpdated Apr 24, 2024

Treating Genital Herpes Infection to Reduce Racial Disparities in the Risk of Severe Maternal Morbidity

An observational study in Genital Herpes Simplex, Maternal Morbidity and Racial Disparities, sponsored by Kaiser Permanente. Recruiting at 1 site in United States. Open to female participants aged 18 Years to 55 Years. Per ClinicalTrials.gov, last updated 2024-04-24.

Sponsored by Kaiser Permanente · Observational

From the registry’s dates

  • Primary completion was expected by Jan 2025, 1 year 9 months ago, but the record still lists the study as recruiting.
  • Started Jan 2023; still recruiting 3 years 10 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
339,000
Ages
18 Years to 55 Years
Sex
Female
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 40 studies in Herpes Genitalis with a site in United States — 1 open to participants now, 2 under way, none of them phase 3. Herpes Genitalis · United States.

Started
2023
with 2 others
Observational
8 of 40
1 open now
Registered
37th of 40
by date

Among the 40 studies in Herpes Genitalis with a site in United States, this one is one of 3 that started in 2023, is one of 8 observational ones, and was the 37th registered.

Herpes Genitalis

70 studies on the registry are indexed under Herpes Genitalis; 3 are open to participants now.

Browse Herpes Genitalis studies →

Open to participants now

1 of the 40 studies in Herpes Genitalis with a site in United States is open now.

A study can be open while its sites in United States have not opened yet or have stopped. Only those recruiting at a site in United States →

Who these studies take

Of the 1 Herpes Genitalis studies recruiting now, 0 (0%) set no upper age limit and 1 (100%) stop at 75 or younger; 0 take children under 18; 0 take healthy volunteers.

This study: 18 Years to 55 Years · female · no healthy volunteers.

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02

Study summary

Severe Maternal Morbidity (SMM) has been associated with maternal mortality, fetal risk, and long-term maternal risk. African American (AA) women are at consistently higher risk than White women. However, factors contributing to these racial disparities are largely unknown and commonly known factors have not been able to explain them, so strategies to reduce them are absent. CDC reports that the rate of GHSV infection is 4 times higher in AA than White women. Studies have shown that pregnant women with genital herpes simplex virus (GHSV) infection are at higher risk of SMM and that treating women with GHSV using existing anti-herpes medications could reduce SMM risk. To address the question of racial disparities in SMM and examine the comparative effectiveness of treating women with GHSV infection to reduce the risk of SMM, the investigators are conducting a large cohort study with a two-stage design, combining an EMR-based cohort (Stage I) with a sub-cohort interview (Stage II) to examine the impact of confounders not available from EMR data. Based on status of GHSV and treatment, 4 cohorts of women will be established: (1) those with GHSV infection receiving treatment early in pregnancy; (2) those with GHSV infection receiving treatment later in pregnancy; (3) those with GHSV infection untreated during pregnancy; and (4) those without GHSV. Given that racial disparities in SMM present serious challenges, the study will provide much needed data to address the effectiveness of treating GHSV on reducing racial disparities in SMM.

Read the detailed description

Severe Maternal Morbidity (SMM), as defined by the CDC, has been repeatedly associated with maternal mortality, fetal risk, and long-term maternal risk. SMM is one of PCORI's research priorities (Special Areas of Emphasis, SAE). Racial disparities in SMM have also been well established, with African American (AA) women having more than twice the risk of SMM than White women However, factors contributing to racial disparities in SMM are largely unknown. Commonly known socio-economic factors have not been able to explain these racial disparities. Due to a lack of understanding of factors contributing to racial disparities in SMM, strategies to reduce them are largely absent.

Recent studies have shown that pregnant women with genital herpes simplex virus (GHSV) infection are at higher risk of pregnancy complications, including SMM. This reported association is supported by strong biological plausibility. Once infected, the virus remains in the body permanently, shedding the virus periodically and causing inflammation in the reproductive tract. The virus is often reactivated during pregnancy due to stress, hormonal changes, and weakened immunity, exacerbating existing inflammation and leading to pregnancy complications, including SMM. At the same time, CDC reports have repeatedly shown that the rate of GHSV infection is 4 times higher in AA women than in White women. Thus, the combination of (a) an increased risk of SMM associated with GHSV infection with (b) high GHSV infection rate in AA makes GHSV a likely contributing factor to the persistently observed racial disparities in SMM. More importantly, recent studies, including a pilot study conducted by the investigators, have shown that treating women with GHSV infection using existing anti-herpes medications could lead to reduction in the risk of SMM. Given that it would benefit AA women more because of their higher GHSV infection rate, the treatment could consequently lead to reduction in racial disparities in SMM. Currently, there is a significant knowledge gap regarding the benefit of treating GHSV infection to reduce the risk of SMM and its racial disparities. Thus, pregnant women with GHSV infection, including many AA women, are not being treated during pregnancy. The current CDC guidelines for treating GHSV infection at 36 weeks of gestation are focused on reducing vertical transmission to newborns; thus, the treatment timing is too late to prevent SMM. Thus, a potentially effective treatment in reducing racial disparities in SMM is not being implemented because of the lack of evidence and the knowledge gap which urgently need to be addressed.

To investigate the comparative effectiveness of treating women with GHSV infection, in comparison to not treating or treating too late, to reduce racial disparities in SMM, the investigators will conduct a large cohort study by leveraging their experience and expertise in studying GHSV infection during pregnancy. The study will consist of pregnant women in four cohorts: (1) women with GHSV infection who received treatment early in pregnancy (before the 3rd trimester); (2) women with GHSV infection who received treatment later in pregnancy (during the 3rd trimester); (3) women with GHSV infection without treatment during pregnancy (untreated); and (4) women without GHSV infection (unexposed controls). Data on GHSV infection and its treatment, SMM diagnosis, and potential confounders are available for all included women from electronic medical records (EMRs). In addition, the study will consist of a sub-cohort of 1,200 participants, selected from each of the four cohorts, who will be interviewed to collect data on additional confounders not available from the EMR. These data will allow the investigators to assess the existence of unmeasured confounders and whether they will impact the results, if any.

The specific aims will address these questions:

Aim 1: Is treating GHSV infection in pregnancy effective in mitigating the racial disparities in SMM? Aim 2: Is treating GHSV infection early in pregnancy more effective than later in pregnancy to mitigate the racial disparities in SMM? Aim 3: Does GHSV infection, if untreated, contribute to racial disparities in the risk of SMM?

The proposed study will address not only one of PCORI research priorities (SAE) in relation to severe maternal morbidity, but also another PCORI priority: reducing racial disparities in health outcomes. The study is also rooted in, and supported by, promising preliminary results and emerging literature with biological plausibility (scientific premise). Unlikely other factors that may contribute to racial disparities that are either very difficult to modify (e.g. sociodemographic factors) or impossible to modify (e.g., genetic factors), if the findings of the pilot study are confirmed, GHSV infection is a modifiable factor that can be treated by existing anti-herpes medications. Thus, the study will fill a knowledge gap which could lead to reduction in racial disparities in SMM through changes in clinical practice of how GHSV infection is treated among pregnant women.

03

Conditions studied

  • Genital Herpes Simplex
  • Maternal Morbidity
  • Racial Disparities

Browse trials for

Keywords

  • GHSV
  • SMM
  • Racial Disparities
04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All KPNC pregnant women during the study period will be eligible for the study.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Kaiser Permanente Northern California Members
  • Pregnant women

Exclusion criteria

Exclusion Criteria:

  • Non Kaiser Permanente Northern California Members
  • Non-pregnant women
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
339,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Genital herpes treated before third trimester

    Pregnant women with genital herpes infection receiving treatment before the 3rd trimester.

  • Genital herpes treated during third trimester

    Pregnant women with genital herpes infection receiving treatment during the 3rd trimester.

  • Genital herpes untreated

    Pregnant women with untreated genital herpes infection.

  • Control Group

    Pregnant women (controls) with neither genital herpes infection nor treatment.

06

What researchers measure

Primary outcomes

  1. Women with SMM

    SMM Diagnoses based on CDC's list of 21 indicators

    Time frame: During labor and delivery

07

Study locations

1 of 1 sites recruiting
  • Division of Research, Kaiser Permanente Northern California
    Oakland, California 94312, United States
    Recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jan 2023 (actual). Primary completion is estimated for Jan 2025, 24 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 17, 2022
First posted
Jun 23, 2022
StartActual
Jan 8, 2023
Primary completionEst.
Jan 31, 2025
CompletionEst.
Apr 30, 2026
Last update
Apr 24, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 24, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05429346
Lead sponsor
Kaiser Permanente
Collaborators
Patient-Centered Outcomes Research Institute
Responsible party
Sponsor
First posted
Jun 23, 2022
Start date
Jan 8, 2023
Primary completion
Jan 31, 2025 (estimated)
Completion
Apr 30, 2026 (estimated)
Last update
Apr 24, 2024

Study contacts

Roxana Odouli, MSPH
Contact
Roxana.Odouli@kp.org
888.381.6818
Sannaz Keyhani, MA
Contact
Sannaz.Keyhani@kp.org
510.326.0174
De-Kun Li, MD, PhD
principal investigator · Division of Research, Kaiser Permanente Northern California

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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