Clinical Trials Directory

Trials / Completed

CompletedNCT01077804

A Study to Evaluate Long-term Impact of VARIVAX Among Children and Adolescents (V210-036)(COMPLETED)

Fifteen Year Follow-up to Evaluate Long-term Effectiveness of VARIVAX Among Children and Adolescents

Status
Completed
Phase
Study type
Observational
Enrollment
7,585 (actual)
Sponsor
Merck Sharp & Dohme LLC · Industry
Sex
All
Age
12 Months – 23 Months
Healthy volunteers
Accepted

Summary

The purpose of these continuing post-licensure studies is to evaluate the long-term effectiveness of VARIVAX® \[Varicella Virus Vaccine Live (Oka/Merck)\] and to assess the impact of the vaccine on the epidemiology of varicella and herpes zoster.

Detailed description

Parents/guardians of the cohort of children vaccinated between 12 and 23 months of age during a six-month period in 1995 (June-November) at KPMCP Northern California were interviewed by telephone at 6-month intervals to ascertain whether their child had varicella or herpes zoster in the 6 months prior to interview. Follow-up continued for a minimum of 14 years after vaccination.

Conditions

Timeline

Start date
1995-06-01
Primary completion
2010-09-01
Completion
2010-11-01
First posted
2010-03-01
Last updated
2017-09-15
Results posted
2011-11-03

Source: ClinicalTrials.gov record NCT01077804. Inclusion in this directory is not an endorsement.

A Study to Evaluate Long-term Impact of VARIVAX Among Children and Adolescents (V210-036)(COMPLETED) (NCT01077804) · Clinical Trials Directory