Skip to content

Study to Estimate the Burden of Herpes Zoster and Postherpetic Neuralgia in Spain

Population Based Surveillance to Estimate the Burden of Herpes Zoster and Postherpetic Neuralgia in Spain

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01521286
Enrollment
552
Registered
2012-01-30
Start date
2012-03-31
Completion date
2015-05-31
Last updated
2015-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Herpes Zoster

Keywords

Spain, cost, complications, incidence, adults, quality of life, Herpes Zoster, Surveillance

Brief summary

The purpose of this study is to collect data on the incidence, complications and impact on quality of life of herpes zoster (HZ) disease in adults \>=50 years of age in Spain. This study will also collect data on costs related to the HZ disease, especially postherpetic neuralgia (PHN)

Interventions

OTHERData collection

HZ and PHN booklet questionnaire and zoster brief pain inventory (ZBPI) questionnaire.

Sponsors

GlaxoSmithKline
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* A male or female \>=50 years of age at the time of study enrolment presenting with acute HZ; * HZ diagnosis for this HZ episode; * is the subject's first outpatient diagnosis; OR * took place at another site/ centre up to seven days before the initial visit for the present study; * Ability to comply with study procedures\*; * Written informed consent obtained from the subject\*. Note: \* will be applicable to secondary objectives only and not for the primary objective to calculate incidence.

Exclusion criteria

• Subject participating in another research study. Note: This

Design outcomes

Primary

MeasureTime frame
Total number of HZ cases as recorded per participating practice, overall and within a specific age group and gender.up to one year

Secondary

MeasureTime frame
Anamnestic information, clinical parameters and complications related to HZ.Between Day 0 and Day 270
Direct medical, direct non-medical and indirect costs related to HZ.Between Day 0 and Day 90
Pain assessment in HZ subjects.At Day 90
Occurrence of PHN, i.e. persistence of HZ-related pain.90, 180, and 270 days after onset of HZ.
Direct medical, direct non-medical and indirect costs related to PHN.At Day 90, Day 180 and Day 270
Pain assessment in PHN subjects.At Day 90, Day 180 and Day 270
Quality of life assessment in PHN subjects.At Day 90, Day 180 and Day 270
Quality of life assessment in HZ subjectsDay 15, Day 30, Day 60 and Day 90

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026