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Status unknownNCT00228202Updated Aug 18, 2006

Genotyping of Cytomegalovirus From Patients in Israel

An observational study in Cytomegalovirus Infections, sponsored by Sheba Medical Center. Status unknown at 1 site in Israel. Open to participants aged 0 Years and older. Per ClinicalTrials.gov, last updated 2006-08-18.

Sponsored by Sheba Medical Center · Observational

The sponsor has not verified this record recently (last verified Jan 2006), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Natural history
Time perspective
Other
Enrollment
100
Ages
0 Years and older
Sex
All
01

Study summary

The researchers select 100 cytomegalovirus (CMV) DNA samples from patients diagnosed with CMV infection. Patients include bone marrow transplant patients, pregnant women and newborns. The researchers determine viral load by real-time polymerase chain reaction (PCR). They amplify CMV-gB sequences by PCR and type by sequencing and restriction fragment length polymorphism (RFLP). The researchers obtain clinical data from patients' records. They examine association between patients' clinical status and CMV-gB genotype and viral load.

Read the detailed description

The study aims at finding association between CMV viral load and viral glycoprotein B genotype and the clinical status of patients suffering from CMV infection. Bone marrow transplant patients are at increased risk of developing severe CMV disease and are routinely followed for viral load. Fetuses are also at high risk for developing severe malformations and neurological defects following maternal primary infection during pregnancy. Therefore amniotic fluid from women diagnosed with CMV infection is examined for CMV presence. Newborns having congenital defects are tested for CMV excretion.

There is not yet any confirmed marker for assessment of the potential severity of the viral infection and for prognosis. Therefore we shall attempt to find association between the viral load and genotype and the clinical status.

CMV DNA samples prepared at the Central Virology Laboratory from clinical specimens obtained from patients for diagnostic purposes will be coded and then subjected to viral load analysis using real-time PCR. The gB genotype will be determined by either of two methods described in the literature: (a) PCR and RFLP (b) PCR and sequencing.

Relevant clinical data will be retrieved from the patients clinical records and saved as coded information to match the samples. Bone marrow transplant patients will be followed for prolonged periods covering repeated viral reactivation events. Clinical records from mothers and newborns will be matched when present. Otherwise maternal and newborn samples will be kept as is.

Statistical analysis will be performed to try and find association between the clinical status of patients, the viral load and the viral genotype.

02

Conditions studied

  • Cytomegalovirus Infections

Keywords

  • cytomegalovirus
  • CMV
  • pregnancy
  • amniotic fluid
  • bone marrow
  • transplantation
  • viral load
  • glycoprotein B
  • genotyping
  • PCR
  • real-time PCR
  • CMV disease
  • Congenital CMV infection
03

In context

Cytomegalovirus Infections

359 studies on the registry are indexed under Cytomegalovirus Infections; 59 are open to participants now.

This study's enrollment of 100 is below the median of 150 across 97 observational studies indexed under Cytomegalovirus Infections.

Browse Cytomegalovirus Infections studies →

Lead sponsor

Sheba Medical Center is the lead sponsor of 660 studies on the registry; 63 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
0 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

  • CMV DNA sample from a transplant patient with CMV disease.
  • CMV DNA from amniotic fluid of women with CMV infection
  • CMV DNA from urine of newborns with congenital defects compatible with CMV.
05

Study design

Observational model
Natural history
Time perspective
Other
Enrollment
100 participants
06

Study locations

1 of 1 sites recruiting
  • Central Virology Laboratory, Chaim Sheba Medical Center Tel-Hashomer
    Ramat Gan, 52621, Israel
    Recruiting
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 18, 2006, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00228202
Lead sponsor
Sheba Medical Center
First posted
Sep 28, 2005
Start date
Sep 2005
Last update
Aug 18, 2006

Study contacts

Ella Mendelson, PhD
Contact
ellamen@sheba.health.gov.il
972-3-530-2421
Naty Keller, MD/PhD
Contact
kelern@sheba.health.gov.il
972-3-530-2304
Naty Keller, MD/PhD
study director · Sheba Medical Center
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2006. You cannot join it, but the record below documents what was studied.

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