Cidofovir as a Treatment for Herpes Simplex in Patients With AIDS
Herpes Simplex, HIV Infections
About this trial
This is an interventional treatment trial for Herpes Simplex focused on measuring AIDS-Related Opportunistic Infections, Herpes Simplex, Acyclovir, Antiviral Agents, Gels, cidofovir
Eligibility Criteria
Inclusion Criteria Patients must have: AIDS diagnosis per CDC criteria. At least partially external mucocutaneous HSV infection confirmed by culture of current outbreak. Current HSV outbreak that is unresponsive to >= 10-day course of acyclovir at 1-4 gm/day po or 15 mg/kg/day IV or in vitro resistance of HSV isolate to acyclovir demonstrated within 60 days of study. Signed, informed consent from parent or legal guardian for patients less than 18 years of age. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Evidence of cervical intraepithelial neoplasia class III (CIN III) on Pap smear (Pap smear required within 6 months of starting study drug). Concurrent Medication: Excluded: Acyclovir, valacyclovir, famciclovir, ganciclovir, foscarnet, topical trifluride, cidofovir injection or other systemic or topical drugs with anti-herpes activity. Required: >= 10 day course acyclovir at 1-4 gm/day po or 15mg/kg/day IV (not required if there is confirmed in vitro resistance to acyclovir).
Sites / Locations
- Mem Med Group Inc
- AIDS Healthcare Foundation Labs
- Sharp Mission Park / Med Group
- Park Ctr for Health / Keith Vrhel
- Potrero Hill Med Ctr
- HIV Primary Care & Consult
- Central Florida Research Initiative
- Braude Mermin Spivey MD PC
- Christie Clinic / Urbana Campus
- Heywood Memorial Hosp
- Gouverneur Hosp
- Central Texas Med Foundation
- Dr Nicholaos Bellos
- Dr Susan M Diamond
- ID Associates