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Herpes Zoster clinical trials

View clinical trials related to Herpes Zoster.

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NCT ID: NCT02052596 Completed - Herpes Zoster Clinical Trials

Study to Assess the Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Subunit (HZ/su) Vaccine (GSK1437173A) When Co-administered With GSK Biologicals' Diphtheria, Tetanus and Pertussis Vaccine (Boostrix®) in Adults Aged 50 Years and Older

Start date: February 7, 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess immunogenicity, reactogenicity and safety of GSK Biologicals' HZ/su vaccine when its first dose is co-administered with the Boostrix® vaccine in adults aged 50 years or older compared to administration of vaccines separately.

NCT ID: NCT02045836 Completed - Herpes Zoster Clinical Trials

Study to Evaluate Immunogenicity and Safety Study of GSK Biologicals' Herpes Zoster (HZ) Vaccine GSK1437173A When Co-administered With Pneumovax 23™ in Adults Aged 50 Years and Older

Start date: March 5, 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the immunogenicity, reactogenicity and safety of the GSK Biologicals HZ/su candidate vaccine when its first dose is co-administered with Pneumovax 23™ vaccine in adults aged 50 years or older.The impact of HZ/su vaccine on Pneumovax 23™ vaccine immune response will also be evaluated.

NCT ID: NCT02026089 Withdrawn - Clinical trials for Persistence of Varicella Immunity

Persistence of Varicella Immunity in Hospital Employees Receiving Varicella Vaccine

Start date: December 2021
Phase: Phase 4
Study type: Interventional

The purpose of the study is to learn more abou how the immune system responds to the chickenpox vaccine in adults who had never had chickenpox as a child and were then vaccinated as an adult. The study aims to learn more about the strength and duration of the protection provided by the vaccine in adults, and to observe the immune response to an additional dose of chickenpox vaccine in adults who had received the vaccine at least 5 years earlier. This is especially relevant to workers in a hospital who may be exposed to chickenpox.

NCT ID: NCT01959841 Completed - Herpes Zoster Clinical Trials

Phase III Study of ASP2151 in Herpes Zoster Patients

Start date: August 2013
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy and safety of ASP2151 (200 mg and 400 mg) in comparison with valaciclovir (VACV) 3000 mg in patients with herpes zoster.

NCT ID: NCT01954251 Completed - Herpes Zoster Clinical Trials

Study to Evaluate the Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A When Co-administered With GSK Biologicals' Seasonal Influenza Vaccine GSK2321138A in Adults Aged 50 Years and Older

Start date: October 3, 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess immunogenicity, reactogenicity and safety of GSK Biologicals' HZ/su vaccine when its first dose is co-administered with the FLU-D-QIV vaccine in adults aged 50 years or older compared to administration of vaccines separately.

NCT ID: NCT01911065 Completed - Herpes Zoster Clinical Trials

T Cell Responses to Varicella Zoster Virus (VZV) Vaccine SLVP020

Start date: September 2010
Phase: Phase 4
Study type: Interventional

In this study the investigators are trying to identify immune signatures that are associated with effective or poor vaccine responses to naturally-acquired herpes zoster virus and the zoster (shingles) vaccine, Zostavax.

NCT ID: NCT01887496 Completed - Chickenpox Clinical Trials

Varicella-related Hospitalizations in Turkey

VARICOMP
Start date: September 2010
Phase: N/A
Study type: Observational

Epidemiological information on varicella complications in children is essential for the development of appropriate immunization recommendations. Economic analyses of varicella immunization are sensitive to the costs of hospitalized cases, so there is a need to validate varicella-related hospitalization data in a country-specific manner. These data also provide a baseline for comparison with data collected after routine varicella immunization to evaluate the overall impact and cost-effectiveness of varicella immunization programs. Knowledge about the cause and incidence of varicella-related hospitalizations in Turkey is limited, center-specific and not sufficiently accurate. The aim of this multicenter study (VARICOMP) was to estimate the annual incidence of pediatric varicella-related hospitalization, describe the associated complications and estimate the annual mortality and economic cost of these cases.

NCT ID: NCT01873365 Completed - Herpes Zoster Clinical Trials

A Study to Assess the Burden of Herpes Zoster and Postherpetic Neuralgia in Japanese Adults Aged Sixty Years and Above

Start date: June 29, 2013
Phase:
Study type: Observational

The study aims to estimate the incidence of herpes zoster (HZ), proportion of postherpetic neuralgia (PHN) and the economic burden and impact on quality of life, in Japanese adults greater than or equal to sixty years of age.

NCT ID: NCT01866566 Recruiting - Varicella Clinical Trials

The Safety and Immunogenicity Research of Live Attenuated Varicella Vaccine After the 2 Doses Vaccination

Start date: June 2013
Phase: Phase 4
Study type: Interventional

Through evaluating the immunogenicity and safety for Varicella vaccine two doses immune procedure we could supply scientific and practical evidence for this two doses immune procedure promotion and management.

NCT ID: NCT01830283 Enrolling by invitation - Varicella Clinical Trials

The Safety, Immunogenicity and Immune Effect Research of the Varicella Vaccine After the 2nd Dose Vaccination

Start date: April 2013
Phase: Phase 4
Study type: Interventional

To investigate the safety, immunogenicity and immune effect of the Varicella vaccine after the 2nd dose vaccination in Chao yang district, Bei jing, since the 2nd varicella vaccination was promoted by Beijing Center for Disease Control and Prevention in November, 2012.