Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Center for Clinical Studies, Texas
Age
50–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Male or female patients of 50 years of age and older.
Patients with a clinical diagnosis of uncomplicated herpes zoster presenting within the first 72 hours of vesicles.
Patients who are willing and able to comply with the requirements of the study.
Patients who are willing and able to give written informed consent.
Average pain score pre-therapy greater or equal than 4 on 10-point Likert scale.
You may not be if
Sexually-active women of childbearing potential, including postmenopausal women less than 1 year since last menses, not employing adequate contraception (approved oral contraceptive, intrauterine device, barrier methods or total abstinence).
Pregnant females and nursing mothers.
Patients with immune dysfunction including congenital immune deficiency, active malignancy of any type, collagen vascular diseases, organ or bone marrow transplantations, known infection with HIV or severe atopic dermatitis.
Patients who have received cytotoxic drugs or immunosuppressive therapy (e.g., chronic systemic corticosteroids) within the previous 3 months.
Patients with evidence of cutaneous or visceral dissemination of herpes zoster infection (cutaneous dissemination is defined as \> 20 discrete lesions outside adjacent dermatomes).
Patients who have received systemic anti-VZV medications or immunomodulatory medications (including interferon) within the previous 4 weeks.
Patients currently receiving probenecid.
Patients with impaired renal function: calculated creatinine clearance of \<30 mL/min using Cockcroft and Gault formula.
Patients with abnormal liver function (alanine transaminase (ALT) or aspartate;transaminase (AST) levels greater than five times the upper limit of the normal range).
Patients with a history of intolerance or hypersensitivity to acyclovir, penciclovir, valacyclovir, famciclovir or gabapentin.
Patients currently receiving therapy with gabapentin or tricyclic antidepressants.
Patients with clinical evidence of ocular involvement of herpes zoster. Patients with herpes zoster of the ophthalmic branch of the trigeminal nerve without evidence of ocular involvement will be included.
