Prospective Studies Clinical Trial
— NPOfficial title:
A Prospective Study to Detect Novel Pathogens and Characterize Emerging Infections
Verified date | October 2017 |
Source | Singapore General Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Infectious disease is the single biggest cause of death worldwide. New infectious agents,such
as the Severe Acute Respiratory Syndrome coronavirus and new strains of influenza continually
emerge and require new investigations to understand pathogen biology and pathogenesis in the
host. Witness the Influenza A pandemic. Concerns about new viruses and their impact on health
and the economy are also increasing. Current alerts sent out by the Ministry of Health (about
the novel coronavirus and the Avian influenza A virus) are but cases in point. These likely
reflect advances in science, which have allowed novel pathogens to be identified.
Because of its geography, Singapore is vulnerable to new pathogens through importation or the
global travel of its citizens. Hence we must be ever ready to meet unexpected challenges
anytime.
On the administrative front, Singapore General Hospital has a Disease Outbreak Task-force
which has in place many plans that can be activated should there be a large-scale epidemic.
What is missing thus far is a program that will enable us to perform scientific studies in
the setting of an epidemic. Hence in this study, we will, in collaboration with the Program
in Emerging Infectious Diseases (EID) in Duke-National University of Singapore Postgraduate
Medical School, attempt to (i) detect novel, previously undescribed pathogens; (ii)
characterize viruses (not necessarily novel but emerging and re-emerging) that are raising
concern or causing clusters or epidemics in the hospital and/or country; (iii) characterize
immune responses to such viruses in healthcare workers as well as patients (those affected by
these viruses and those exposed to the affected). The techniques that will be used will be
those not routinely available in a hospital's service labs.
Some patients will remain undiagnosable with the best available technology. Since new
laboratory tools that can detect previously undiagnosed pathogens may become available in the
future, the study also aims to archive specimens from patients whose illnesses remain
undiagnosed.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | June 2020 |
Est. primary completion date | January 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: Any person admitted to Singapore General Hospital or seen as an outpatient in the Specialist Outpatient Clinic who has: 1. clinical history and/or clinical syndromes compatible with a suspected novel/re-emerging infective etiological agent Exclusion Criteria: 1. Any person unable to give informed consent and for whom no legally acceptable representative is available |
Country | Name | City | State |
---|---|---|---|
Singapore | Singapore General Hospital | Singapore |
Lead Sponsor | Collaborator |
---|---|
Singapore General Hospital |
Singapore,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Detecting of Novel Pathogens | Clinical data collection through case records, and interview of patients or next-of-kin or friend in the event information is unavailable or incompletely documented in the case records. Sample collection will be performed according to the following frequency: First day of enrolment: blood draw (by weight) not more than 20ml, nasal (and/or nasopharyngeal ) and/or throat swab, stool and urine sample. On days 2, 3, 5, 7, 10, 14 and 28: blood (by weight) not more than 10 ml, nasal (and/or nasopharyngeal l) and/or throat swab, stool and urine sample. On D28, blood (by weight) not more than 20ml, will be drawn as most immune response changes manifest by then. If available, urine and stool sample will be collected. If the subject is intubated, endotracheal aspirate will replace nasal and throat swab. Sample collection for research will be done at the same time as samples for clinical testing as far as possible, to minimize patient discomfort. |
Day 1 - Day 28 of recruitment |
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