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Herpes Zoster clinical trials

View clinical trials related to Herpes Zoster.

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NCT ID: NCT00209352 Completed - Clinical trials for VZV Infection After Bone Marrow Transplantation

Long-Term Oral Acyclovir Usage to Prevent Herpes Zoster Virus Infection After Bone Marrow Transplant

Start date: June 1985
Phase: Phase 3
Study type: Interventional

The objective of this study is to prevent reactivation of herpes zoster during the first year after transplant.

NCT ID: NCT00138255 Terminated - Measles Clinical Trials

Responses of Premature Infants to Measles-Mumps-Rubella (MMR) and Varicella Vaccines

Start date: June 2004
Phase: Phase 4
Study type: Observational

The purpose of this study is to see if the MMR and chickenpox vaccines work as well in premature infants as in children that were carried to full term. A group of children who were carried full-term will be matched for age, sex, and race and will be used for comparison.

NCT ID: NCT00130793 Completed - Herpes Zoster Clinical Trials

A Study to Evaluate Safety, Tolerability, and Immunogenicity of an Investigational Zoster Vaccine In Subjects With a History of Varicella (Chickenpox)(V211-010)(COMPLETED)

Start date: August 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the refrigerator-stable formulation of an investigational vaccine has a comparable immune response (the body's ability to protect against disease) and safety profile to that of the freezer-stable formulation of the vaccine.

NCT ID: NCT00127608 Completed - Varicella Clinical Trials

Detection and Characterisation of Varicella Zoster Virus From Dermal Lesions of Chickenpox-infected Patients

Start date: June 7, 2005
Phase: Phase 3
Study type: Interventional

This study is conducted in order to collect clinical samples from patients who are diagnosed of having chickenpox infection. The results of this study will provide basic scientific information about chickenpox disease.

NCT ID: NCT00127023 Completed - Measles Clinical Trials

Immunogenicity and Safety of a Combined Vaccine to Prevent Measles, Mumps, Rubella and Chickenpox Diseases

Start date: May 2005
Phase: Phase 3
Study type: Interventional

This is a study to evaluate the immunogenicity and safety of GlaxoSmithKline (GSK) Biologicals combined measles-mumps-rubella varicella candidate vaccine given to healthy children in their second year of life.

NCT ID: NCT00127010 Completed - Measles Clinical Trials

Immunogenicity and Safety of a Combined Vaccine to Prevent Measles, Mumps, Rubella and Chickenpox Diseases

Start date: November 2005
Phase: Phase 3
Study type: Interventional

This is a study to evaluate the immunogenicity and safety of GlaxoSmithKline (GSK) Biologicals combined measles-mumps-rubella varicella candidate vaccine given to healthy children in their second year of life.

NCT ID: NCT00126997 Completed - Measles Clinical Trials

Immunogenicity and Safety of Combined Vaccine to Prevent Measles, Mumps, Rubella and Chickenpox Diseases

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

This is a study to assess the immunogenicity and safety of GlaxoSmithKline (GSK) Biologicals live attenuated measles-mumps-rubella-varicella vaccine given to healthy children in their second year of life.

NCT ID: NCT00118885 Completed - Aging Clinical Trials

Shingles: Immune Effects of Tai Chi

Start date: July 2001
Phase: Phase 2
Study type: Interventional

The purpose of this trial is to evaluate the effects of Tai Chi Chih versus Health Education on shingles immunity in older adults as measured by unstimulated and vaccine-stimulated responses. The secondary goal of the study is to determine the effects of Tai Chi Chih versus Health Education on measures of health functioning, depressive symptoms, and health behaviors in the elderly.

NCT ID: NCT00115310 Completed - Pain Clinical Trials

Study of NGX-4010 for the Treatment of Postherpetic Neuralgia

Start date: June 2005
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess the efficacy and safety of NGX-4010 applied for 60 minutes for the treatment of postherpetic neuralgia (PHN).

NCT ID: NCT00109122 Completed - Shingles Clinical Trials

Safety, Tolerability, and the Body's Ability to Develop Resistance to an Investigational Vaccine for Shingles (V211-007)

Start date: November 2001
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the immunity (the body's protection) against shingles after receiving two doses of an investigational vaccine or placebo (a look alike vaccine with no active ingredients).