Clinical Trials Directory

Trials / Completed

CompletedNCT00526864

Measuring Herpes Zoster and PHN Associated Burden of Illness and Health Care Utilization Costs in Thailand

Measuring Herpes Zoster and Post-Herpetic Neuralgia Associated Burden of Illness and Health Care Utilization and Costs in Thailand

Status
Completed
Phase
Study type
Observational
Enrollment
180 (actual)
Sponsor
Mahidol University · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

Total 7 institutions will be recruited i.e. Clinical Infectious Disease Research Unit Department of Clinical Tropical Medicine, Faculty of Tropical Medicine Mahidol University,Bamrasnaradura Infectious Disease Institute ,Pramonkutklao Hospital,Rajavithi Hospital,NationalCancerInstitute,Institute of Dermatology,Raj Pracha Samasai Institute OBJECTIVES * Measure the burden of illness due to herpes zoster (Zoster) and post-herpetic neuralgia (PHN) (severity and duration); * Assess the quality of life (QoL) and quality adjusted life years (QALY) lost due to Zoster and PHN; * Describe health care resource utilization associated with Zoster and PHN; * Describe the direct and indirect costs per case of Zoster and PHN

Detailed description

This will be a prospective cohort study of patients presenting with Zoster rash in 7 specialized institutions in Thailand. Subjects will be entered in the cohort at the time of presentation with Zoster rash. After the baseline assessment (day 0) that will be conducted at the investigator's office there will be 4 assessments (prospective part of the study) that will be conducted at day 7, month 1, month 3 and month 6. We expect that there will be approximately 150 patients included in the study cohort. Cohort assembly will take place between April 2007 and October 2007. The study will be conducted in 3 groups Eligible patients for each group will include * Group A: Both male and female patients ≥ 50 years of age with Zoster rash. * Group B: Both HIV infected male and female patients ≥ 20 years of age with Zoster rash. * Group C: Both Oncology male and female patients ≥ 20 years of age who on chemotherapy with Zoster rash. Key exclusion criteria includes patient who refuses to sign informed consent.

Conditions

Timeline

Start date
2007-05-01
Primary completion
2008-07-01
Completion
2008-07-01
First posted
2007-09-10
Last updated
2015-09-23

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT00526864. Inclusion in this directory is not an endorsement.