30-Day Trial of Oral Valtrex or Valtrex Plus Aspirin on Shedding of HSV DNA in Tears and Saliva of Volunteers
Primary Purpose
Herpes Simplex
Status
Unknown status
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
valacyclovir hydrochloride
placebo
valacyclovir plus aspirin
Sponsored by
About this trial
This is an interventional prevention trial for Herpes Simplex focused on measuring HSV DNA, volunteers
Eligibility Criteria
Inclusion Criteria:
- either sex
- any race
- over age of 21 years
Exclusion Criteria:
- have active ocular herpetic lesion
- had ocular herpetic lesion in past 30 days
- taking systemic or oral antiviral drugs
- have taken antiviral drugs in the past 30 days
- taking aspirin or NSAIDs
- have dry eyes
- have hypersensitivity to acyclovir or valacyclovir
- have hypersensitivity of contraindication to use of aspirin
- have bleeding disorder
- have GI ulcer
- have kidney impairment
- are pregnant or nursing
- have participated in a clinical trial in the past 30 days
Sites / Locations
- LSU Eye CenterRecruiting
- Children's HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Experimental
Arm Label
1
2
3
Arm Description
placebo, 6 capsules per day for 30 days
500 mg Valtrex one capsule per day plus 5 capsules of placebo per day for 30 days
500 mg Valtrex capsule one per day, Acetylsalicylic acid (aspirin) 325 mg capsules three per day, plus 2 placebo capsules per day for 30 days
Outcomes
Primary Outcome Measures
Cessation of DNA shedding above the positive detection threshold
Secondary Outcome Measures
Full Information
NCT ID
NCT00587496
First Posted
December 21, 2007
Last Updated
December 21, 2007
Sponsor
National Eye Institute (NEI)
1. Study Identification
Unique Protocol Identification Number
NCT00587496
Brief Title
30-Day Trial of Oral Valtrex or Valtrex Plus Aspirin on Shedding of HSV DNA in Tears and Saliva of Volunteers
Official Title
A 30-Day Double-Masked Study to Determine the Effect of Oral Valacyclovir or Oral Valacyclovir Plus Aspirin on the Shedding of Herpes Simplex Virus DNA in the Tears and Saliva of Volunteers Without Clinical Signs of Ocular Herpetic Disease
Study Type
Interventional
2. Study Status
Record Verification Date
December 2007
Overall Recruitment Status
Unknown status
Study Start Date
April 2006 (undefined)
Primary Completion Date
July 2008 (Anticipated)
Study Completion Date
July 2008 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
National Eye Institute (NEI)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine whether oral Valtrex alone or in combination with aspirin will reduce the shedding of herpes simplex virus DNA in the tears and saliva from volunteers with no evidence of ocular herpes infection. The secretion of virus into the tears and saliva might make people more susceptible to virus infection in the future if their immune system becomes deficient. The study will also try to determine if there is a correlation between shedding of viral DNA and herpes virus antibodies in serum and to determine if subjects are carriers of a special form of a gene in their blood cells, the presence of which may suggest the possibility of an increased susceptability to herpes and to Alzheimer's disease and heart disease.
Detailed Description
Published studies have shown that treatment with oral acyclovir reduced clinical recurrences of ocular herpetic keratitis by about 40-50 %8, and treatment with valacyclovir, a more soluble prodrug of acyclovir, reduced the risk of transmission of genital herpes9, 10, 11. For this study, we will use the dose of valacyclovir that was shown effective in reducing the risk of transmission of HSV-2.9 The dose of 325 mg aspirin three times a day was chosen based on our experience with mice and other laboratory animals12. If it is effective and well tolerated at this dose, in future studies we will attempt to use lower doses and determine if they too may be effective.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Herpes Simplex
Keywords
HSV DNA, volunteers
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
placebo, 6 capsules per day for 30 days
Arm Title
2
Arm Type
Experimental
Arm Description
500 mg Valtrex one capsule per day plus 5 capsules of placebo per day for 30 days
Arm Title
3
Arm Type
Experimental
Arm Description
500 mg Valtrex capsule one per day, Acetylsalicylic acid (aspirin) 325 mg capsules three per day, plus 2 placebo capsules per day for 30 days
Intervention Type
Drug
Intervention Name(s)
valacyclovir hydrochloride
Other Intervention Name(s)
Valtrex
Intervention Description
500 mg capsule, one per day for 30 days
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
lactose placebo capsule, six per day for 30 days
Intervention Type
Drug
Intervention Name(s)
valacyclovir plus aspirin
Intervention Description
500 mg valacyclovir capsule, one per day for 30 days 325 mg acetyl salicylic acid (aspirin) capsule, three per day for 30 days placebo capsule, two per day for 30 days
Primary Outcome Measure Information:
Title
Cessation of DNA shedding above the positive detection threshold
Time Frame
30 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
either sex
any race
over age of 21 years
Exclusion Criteria:
have active ocular herpetic lesion
had ocular herpetic lesion in past 30 days
taking systemic or oral antiviral drugs
have taken antiviral drugs in the past 30 days
taking aspirin or NSAIDs
have dry eyes
have hypersensitivity to acyclovir or valacyclovir
have hypersensitivity of contraindication to use of aspirin
have bleeding disorder
have GI ulcer
have kidney impairment
are pregnant or nursing
have participated in a clinical trial in the past 30 days
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Emily D Varnell, BS
Phone
504 568-2254
Email
evarne@lsuhsc.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Robin Cooper, BS
Phone
504 568-2815
Email
rcoope@lsuhsc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Herbert E Kaufman, MD
Organizational Affiliation
LSU Eye Center, LSU Health Sciences Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
LSU Eye Center
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70112
Country
United States
Individual Site Status
Recruiting
Facility Name
Children's Hospital
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70118
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Herbert E Kaufman, MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
15623779
Citation
Kaufman HE, Azcuy AM, Varnell ED, Sloop GD, Thompson HW, Hill JM. HSV-1 DNA in tears and saliva of normal adults. Invest Ophthalmol Vis Sci. 2005 Jan;46(1):241-7. doi: 10.1167/iovs.04-0614.
Results Reference
background
PubMed Identifier
4295319
Citation
Lindgren KM, Douglas RG Jr, Couch RB. Significance of Herpesvirus hominis in respiratory secretions of man. N Engl J Med. 1968 Mar 7;278(10):517-23. doi: 10.1056/NEJM196803072781001. No abstract available.
Results Reference
background
PubMed Identifier
4312871
Citation
Douglas RG Jr, Couch RB. A prospective study of chronic herpes simplex virus infection and recurrent herpes labialis in humans. J Immunol. 1970 Feb;104(2):289-95. No abstract available.
Results Reference
background
PubMed Identifier
9250929
Citation
Scott DA, Coulter WA, Biagioni PA, O'Neill HO, Lamey PJ. Detection of herpes simplex virus type 1 shedding in the oral cavity by polymerase chain reaction and enzyme-linked immunosorbent assay at the prodromal stage of recrudescent herpes labialis. J Oral Pathol Med. 1997 Aug;26(7):305-9. doi: 10.1111/j.1600-0714.1997.tb00220.x.
Results Reference
background
PubMed Identifier
9041386
Citation
Hobson A, Wald A, Wright N, Corey L. Evaluation of a quantitative competitive PCR assay for measuring herpes simplex virus DNA content in genital tract secretions. J Clin Microbiol. 1997 Mar;35(3):548-52. doi: 10.1128/jcm.35.3.548-552.1997.
Results Reference
background
PubMed Identifier
10325351
Citation
Ryncarz AJ, Goddard J, Wald A, Huang ML, Roizman B, Corey L. Development of a high-throughput quantitative assay for detecting herpes simplex virus DNA in clinical samples. J Clin Microbiol. 1999 Jun;37(6):1941-7. doi: 10.1128/JCM.37.6.1941-1947.1999.
Results Reference
background
PubMed Identifier
10878056
Citation
Kessler HH, Muhlbauer G, Rinner B, Stelzl E, Berger A, Dorr HW, Santner B, Marth E, Rabenau H. Detection of Herpes simplex virus DNA by real-time PCR. J Clin Microbiol. 2000 Jul;38(7):2638-42. doi: 10.1128/JCM.38.7.2638-2642.2000.
Results Reference
background
PubMed Identifier
9696640
Citation
Acyclovir for the prevention of recurrent herpes simplex virus eye disease. Herpetic Eye Disease Study Group. N Engl J Med. 1998 Jul 30;339(5):300-6. doi: 10.1056/NEJM199807303390503.
Results Reference
background
PubMed Identifier
14702423
Citation
Corey L, Wald A, Patel R, Sacks SL, Tyring SK, Warren T, Douglas JM Jr, Paavonen J, Morrow RA, Beutner KR, Stratchounsky LS, Mertz G, Keene ON, Watson HA, Tait D, Vargas-Cortes M; Valacyclovir HSV Transmission Study Group. Once-daily valacyclovir to reduce the risk of transmission of genital herpes. N Engl J Med. 2004 Jan 1;350(1):11-20. doi: 10.1056/NEJMoa035144.
Results Reference
background
PubMed Identifier
14702430
Citation
Crumpacker CS. Use of antiviral drugs to prevent herpesvirus transmission. N Engl J Med. 2004 Jan 1;350(1):67-8. doi: 10.1056/NEJMe038189. No abstract available.
Results Reference
background
PubMed Identifier
15512958
Citation
Gebhardt BM, Varnell ED, Kaufman HE. Acetylsalicylic acid reduces viral shedding induced by thermal stress. Curr Eye Res. 2004 Aug-Sep;29(2-3):119-25. doi: 10.1080/02713680490504588.
Results Reference
background
Citation
Anon. New indications. Valtrex. FDA Drug Approvals 38:572-573, 2003.
Results Reference
background
Citation
Sheskin DJ. Handbook of Parametric and Nonparametric tatistical Procedures. 2nd Edition. Chapman & Hall/CRC, Boca Raton, FL pp. 982,2000.
Results Reference
background
Learn more about this trial
30-Day Trial of Oral Valtrex or Valtrex Plus Aspirin on Shedding of HSV DNA in Tears and Saliva of Volunteers
We'll reach out to this number within 24 hrs