Evaluation of the HSV 1 & 2 Assay in Specimens From Symptomatic Subjects
Status: | Active, not recruiting |
---|---|
Conditions: | Infectious Disease |
Therapuetic Areas: | Immunology / Infectious Diseases |
Healthy: | No |
Age Range: | Any |
Updated: | 4/21/2016 |
Start Date: | December 2014 |
End Date: | June 2016 |
Clinical Evaluation of the Aptima® Herpes Simplex Viruses 1 & 2 Assay on the Panther® System in Swab Specimens From Symptomatic Subjects Presenting With a Suspected Herpes Lesion(s)
This clinical performance study is being conducted to evaluate the performance of the Aptima
Herpes Simplex Viruses 1 & 2 assay for detection of herpes simplex virus (HSV) type 1
(HSV-1) and HSV type 2 (HSV-2) in swab samples prospectively collected from suspected HSV
lesions in the male anogenital region, the female anogenital region, the oral cavity and
other mucomembranous or mucocutaneous areas of the face (oral/facial), and the skin.
Specimens collected using swabs from viral transport medium (VTM)collection kits and Aptima
swab collection kits will be evaluated.
Herpes Simplex Viruses 1 & 2 assay for detection of herpes simplex virus (HSV) type 1
(HSV-1) and HSV type 2 (HSV-2) in swab samples prospectively collected from suspected HSV
lesions in the male anogenital region, the female anogenital region, the oral cavity and
other mucomembranous or mucocutaneous areas of the face (oral/facial), and the skin.
Specimens collected using swabs from viral transport medium (VTM)collection kits and Aptima
swab collection kits will be evaluated.
Inclusion Criteria:
- The subject has at least 1 active lesion (lesion with exudates and cellular material;
eg, vesicle, ulcer) that is suspected to be caused by HSV (as determined by the
clinician)
- The subject and/or legally authorized representative is willing and able to provide
consent prior to study participation (a minor will need the documented consent of
his/her parent or legal guardian, unless the site has an institutional review
board-approved waiver for parental consent for minors)
Exclusion Criteria:
- The subject has only HSV lesions without exudates and cellular material
- The subject used a topical or oral antiviral medication used to treat HSV within 21
days of enrollment
- Subject already participated in this study
- Subject has a history of illness that the principal investigator (PI) or designee
considers could interfere with or affect the conduct, results, and/or completion of
the study
- Subject has a history of illness that the PI or designee considers could create an
unacceptable risk to the subject if enrolled in the study
We found this trial at
22
sites
Los Angeles, California 90069
Principal Investigator: Anthony Mills, MD
Phone: 310-550-2271
Click here to add this to my saved trials
1720 2nd Ave S
Birmingham, Alabama 35233
Birmingham, Alabama 35233
(205) 934-4011
Principal Investigator: Jane Schwebke, MD
Phone: 205-975-5665
University of Alabama at Birmingham The University of Alabama at Birmingham (UAB) traces its roots...
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Houston, Texas 77023
Principal Investigator: Paul Fine, MD
Phone: 713-831-6553
Click here to add this to my saved trials
340 W 10th St #6200
Indianapolis, Indiana 46202
Indianapolis, Indiana 46202
(317) 274-3772
Principal Investigator: Kenneth Fife, MD
Phone: 317-274-8115
Indiana University School of Medicine With more than 2,000 students in 2013, the Indiana University...
Click here to add this to my saved trials
884 Lakeland Drive
Jackson, Mississippi 39216
Jackson, Mississippi 39216
Principal Investigator: Leandro Mena, MD
Phone: 601-984-5560
Click here to add this to my saved trials
Click here to add this to my saved trials
New Haven, Connecticut 06520
Principal Investigator: Michael Kozal, MD
Phone: 203-737-4040
Click here to add this to my saved trials
New Orleans, Louisiana 70112
Principal Investigator: Stephanie N Taylor, MD
Phone: 504-568-4132
Click here to add this to my saved trials
10040 Regency Cir
Omaha, Nebraska 68114
Omaha, Nebraska 68114
(402) 934-0044
Principal Investigator: Michael Dunn, MD
Phone: 402-934-0044
Quality Clinical Research, Inc. Welcome to Quality Clinical Research. We originated here in Omaha, NE...
Click here to add this to my saved trials
Philadephia, Pennsylvania 19107
Principal Investigator: Joel Lebed, DO
Phone: 267-514-2098
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Shreveport, Louisiana 71103
Principal Investigator: John Vanchiere, MD, PhD
Phone: 318-675-6081
Click here to add this to my saved trials
Click here to add this to my saved trials
Webster, Texas 77598
Principal Investigator: Stephen Tyring, MD
Phone: 281-333-2288
Click here to add this to my saved trials