Skip to main content
MedPathMedPath Home
Clinical Trials/ACTRN12608000176369
ACTRN12608000176369
Not yet recruiting
未知

A prospective study to examine the effectiveness and safety of neuraminidase inhibitors in index cases with presumed pandemic influenza infection

ational Centre in HIV Epidemiology and Clinical Research (NCHECR)0 sites1,000 target enrollmentApril 9, 2008
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
ConditionsPandemic influenzaInfection - Other infectious diseases

Overview

Phase
未知
Intervention
Not specified
Conditions
Pandemic influenza
Sponsor
ational Centre in HIV Epidemiology and Clinical Research (NCHECR)
Enrollment
1000
Status
Not yet recruiting
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 9, 2008
End Date
TBD
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
ational Centre in HIV Epidemiology and Clinical Research (NCHECR)

Eligibility Criteria

Inclusion Criteria

  • •1\. Clinical diagnosis of pandemic influenza (consistent with the applicable clinical case definition)
  • •2\. Provision of written informed consent or equivalent
  • •3\. Intention to commence treatment with a neuraminidase inhibitor

Exclusion Criteria

  • •There are no exclusion criteria.

Outcomes

Primary Outcomes

Not specified

Similar Trials

Not yet recruiting
Not Applicable
A prospective study to examine the effectiveness and safety of antivirals in volunteers who receive short-term prophylaxis against pandemic influenza
ACTRN12608000179336ational Centre in HIV Epidemiology and Clinical Research500
Not yet recruiting
Not Applicable
A prospective study to examine the effectiveness and safety of neuraminidase inhibitors in volunteers who receive long-term prophylaxis against pandemic influenza: PIPET B
ACTRN12608000178347ational Centre in HIV Epidemiology and Clinical Research (NCHECR)1,000
Completed
Not Applicable
Prospective study to assess the effectiveness of an integrative primary care approach versus standard primary care management of chronic musculoskeletal pain.
NL-OMON36897ouis Bolk Instituut268
Active, not recruiting
Phase 1
A prospective study to assess the effectiveness of lignocaine versus normal saline in the reduction of pain associated with dressing removal in finger tip injuriesFinger tip injuries
EUCTR2005-005591-32-GBDerby Hospitals NHS Foundation Trust20
Completed
Not Applicable
A prospective study to assess the effectiveness of lignocaine versus normal saline in the reduction of pain associated with dressing removal in fingertip injuries
ISRCTN59113767Record Provided by the NHSTCT Register - 2007 Update - Department of Health98