Abstract | OBJECTIVE: DESIGN: A double-blind, randomized, controlled, multicenter clinical trial in which patients received 7 days of treatment and were followed up for 24 weeks. SETTINGS: Patients reported directly to specialist centers or were referred from primary care centers. PATIENTS: There were 597 otherwise healthy immunocompetent outpatients, aged 50 years and older, who presented within 72 hours of onset of zoster rash. INTERVENTIONS: MAIN OUTCOME MEASURES: RESULTS: CONCLUSIONS:
|
Authors | S K Tyring, K R Beutner, B A Tucker, W C Anderson, R J Crooks |
Journal | Archives of family medicine
(Arch Fam Med)
2000 Sep-Oct
Vol. 9
Issue 9
Pg. 863-9
ISSN: 1063-3987 [Print] United States |
PMID | 11031393
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Antiviral Agents
- 2-Aminopurine
- Valine
- Valacyclovir
- Famciclovir
- Acyclovir
|
Topics |
- 2-Aminopurine
(analogs & derivatives, economics, therapeutic use)
- Acyclovir
(analogs & derivatives, economics, therapeutic use)
- Aged
- Antiviral Agents
(economics, therapeutic use)
- Cost-Benefit Analysis
- Double-Blind Method
- Famciclovir
- Female
- Herpes Zoster
(drug therapy)
- Humans
- Male
- Middle Aged
- Neuralgia
(etiology, prevention & control)
- Pain
(etiology, prevention & control)
- Proportional Hazards Models
- Time Factors
- Valacyclovir
- Valine
(analogs & derivatives, economics, therapeutic use)
|