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Herpes clinical trials

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NCT ID: NCT04664127 Completed - Herpes Simplex Clinical Trials

Study of the Efficacy and Safety of Combined Treatment of Patients With Severe Herpes Simplex (HSV) Infection by Valacyclovir and Interferon Inducer Kagocel

Start date: October 30, 2017
Phase:
Study type: Observational

This study examined the efficacy, safety and benefits of modern treatment and changes in the dynamics of the life of adult patients quality with severe herpes simplex in the current medical practice when combined therapy by acyclic nucleoside Valacyclovir and antiviral agent Kagocel versus monotherapy by Valacyclovir. This study also evaluated the structure of herpesvirus infections and the rate of mixed variants of the course, the rate of exacerbations of herpes simplex, the time of disappearance of human herpesvirus isolation and the features of the immune phenotype of patients taking different types of therapy.

NCT ID: NCT02092233 Completed - Herpes Clinical Trials

A Two Arm, Multi-Site Clinical Evaluation of the ARIES HSV 1&2 Assay in Symptomatic Patients

Start date: January 2014
Phase: N/A
Study type: Observational

The ARIES HSV 1&2 Assay is a PCR based test for the direct detection and typing of herpes simplex virus (HSV 1 & 2) DNA. The objective is to establish the diagnostic accuracy of ARIES HSV-1&2 Assay.

NCT ID: NCT01477879 Completed - Herpes Clinical Trials

Hsv 1 and 2 Gowey Protocol Versus Placebo

Start date: January 2011
Phase: Phase 1/Phase 2
Study type: Interventional

This study will compare efficacy of versabase gel with 20% sarracenia purpurea versus placebo applied every 3-4 hours to herpes lesions.

NCT ID: NCT01321515 Completed - Herpes Clinical Trials

Bioequivalency Study of Famciclovir 500 mg Tablets Under Fasted Conditions

Start date: July 2007
Phase: N/A
Study type: Interventional

The objective of this study was to prove the bioequivalence of Famciclovir 500 mg Tablets under fasting conditions.

NCT ID: NCT01321502 Completed - Herpes Clinical Trials

Bioequivalency Study of Famciclovir 500 mg Tablets Under Fed Conditions

Start date: July 2007
Phase: N/A
Study type: Interventional

The objective of this study was to prove the bioequivalence of Famciclovir 500 mg Tablets under fed conditions.

NCT ID: NCT00362596 Completed - HIV Clinical Trials

A Randomized Controlled Trial of Acyclovir Among HIV and HSV-2 Co-Infected Women, Chiang Rai, Thailand

Start date: January 2005
Phase: Phase 4
Study type: Interventional

Herpes infection is an important co-factor in HIV transmission. A recent meta-analysis demonstrated that HSV infection contributed to a 2-fold increased risk of HIV transmission. Suppressive therapy with acyclovir has been a method proposed to reduce HIV transmission. We are conducting a randomized controlled cross-over trial to evaluate the effect of acyclovir suppressive therapy on HIV genital shedding in women co-infected with HIV-1 and Herpes Simplex Virus Type-2 (HSV-2) in Thailand.