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N/A N=12,550

Identification of Herpes Simplex Virus (HSV) Shedding in the Female Genital Tract of Pregnant and Nonpregnant Women by GeneXpert PCR, Routine PCR, and Culture

Herpes Simplex Virus

Enrolled (actual)
12,550
Serious AEs
0.0%
Results posted
Sep 2020
Primary outcome: Primary: Sensitivity of Detection of HSV DNA by GeneXpert PCR From Specimens Obtained From the Genital Tract of Non-pregnant Women in STI Clinics, as Compared With HSV Culture — 100 Sensitivity (percent positive)

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Genexpert assay (Device)
Age
Adult, Older Adult · 19+ yrs
Sex
Female
Sponsor
University of Alabama at Birmingham
Primary completion
Dec 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Sensitivity of Detection of HSV DNA by GeneXpert PCR From Specimens Obtained From the Genital Tract of Non-pregnant Women in STI Clinics, as Compared With HSV Culture
100
PRIMARY
Positive Percent Agreement of Detection of HSV DNA by GeneXpert PCR From Specimens Obtained From Genital Tract of Pregnant Women, as Compared With Routine PCR Detection of Viral DNA
80
PRIMARY
Negative Percent Agreement of Detection of HSV DNA by GeneXpert PCR From Specimens Obtained From Genital Tract of Pregnant Women, as Compared With Routine PCR Detection of Viral DNA
99.2

Summary

PCR detection of HSV DNA shedding in the female genital tract using the GeneXpert system (Cepheid, Sunnyvale CA) will be compared with traditional (routine) PCR (pregnant and nonpregnant women) and with HSV culture (nonpregnant women). The GeneXpert system performs all sample-processing steps and real-time PCR in a single integrated cartridge. The standard cartridge is an inexpensive disposable plastic cartridge with filtration and ultrasonic lysis capabilities. It consists chiefly of several combined molded plastic components: a cartridge body containing eleven fluid reservoirs or chambers along with an attached PCR tube, a specialized valve body with an ultrasonic interface containing a sub-micron filter and glass lysis beads, and a rotary valve with an axial syringe barrel. The operation of the cartridge is simple. The rotary valve contains an inlet and an outlet port. Fluid such as a sample buffer can be drawn up into a syringe drive through the inlet port of the rotary valve and then dispensed into any other chamber within the cartridge by rotating the valve and expelling the fluid through the outlet port. The fluid can either be passed through a filter contained within the valve assembly or it can be passed directly into the next chamber without filtration, depending on the path that is chosen. The cartridge fluidics and subsequent real-time PCR all are performed within the GeneXpert instrument. The GeneXpert contains multiple modules (ICORE units) that can be independently programmed to drive the syringe/rotary valve, and to perform four-color real-time PCR. Each cartridge fits inside one module, and all processing, PCR, and analysis steps are performed automatically. Each ICORE module can be run and analyzed independently, so batching of samples is unnecessary.

Eligibility Criteria

Inclusion Criteria:•Signed Informed Consent from woman

•≥ 19 years of age

  • Female gender
  • In active labor with a viable fetus, OR non-pregnant and being evaluated in STI clinics for herpetic genital lesions

Exclusion Criteria:•For women in active labor, active herpetic lesions in the genital region

  • Receipt of acyclovir, valacyclovir, or famciclovir within the previous 14 days
  • Known HIV infection
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01878383). 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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