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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00807378
Other study ID # RH-CMR-004
Secondary ID
Status Completed
Phase N/A
First received December 9, 2008
Last updated May 19, 2010
Start date July 2008
Est. completion date March 2010

Study information

Verified date May 2010
Source Rajavithi Hospital
Contact n/a
Is FDA regulated No
Health authority Thailand: Ministry of Public Health
Study type Observational

Clinical Trial Summary

This study of neurotropic viral infection and Tuberculous CNS infection is the comprehensive investigation of CSF PCR arrays (Hybrydiaztion technique,Sybergreen and Taqman real time PCR arrays of CSF ) in suspected cases of viral CNS infection, Tuberculous CNS infection in both AIDS and non AIDS patients.

Patients with clinical viral encephalitis and all meningoencephalitis including all patients with HIV/AIDS CSF and non AIDS will be banked and test for RNA and DNA viral sequence by Real time PCR arrays and IS6110 gene of Mycobacterium tuberculosis. Clinical data and final diagnosis will be used to analyze the result of this PCR arrays technique compared to clinical gold standard criteria.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date March 2010
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender Both
Age group 15 Years and older
Eligibility Inclusion Criteria:

1. AGE MORE THAN 15 YRS

2. ABLE TO INFORM CONSENT BY THEMSELF OR THEIR PARENT

3. SUSPECTED CNS VIRAL INFECTION

Exclusion Criteria:

1. UNABLE/CONTRAINDICATED FOR LUMBAR PUNCTURE OR CSF COLLECTION

2. WITHDRAW CONSENT

3. SUSPECTED SEVERE OR VILURENT VIRAL INFECTION SUCH AS H5N1/SARS INFECTION

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Intervention

Other:
LUMBAR PUNCTURE
LUMBAR PUNCTURE FFOR CSF COLLECTION

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Rajavithi Hospital Rajavithi Biomolecular Research Center