Last updated: 12/26/2019 10:40:04

GSK study ID
108288
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title:
Trial description:
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
2008-29-07
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Infections, Papillomavirus
Product
SB580299
Collaborators
Not applicable
Study date(s)
December 2006 to July 2008
Type
Observational
Phase
Not applicable

Participation criteria

Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable

Trial location(s)

Location
Status
Contact us
Contact us
Location
GSK Investigational Site
Almada, Portugal, 2805-267
Status
Study Complete
Location
GSK Investigational Site
Amadora, Portugal, 2720-276
Status
Study Complete
Location
GSK Investigational Site
Athens, Greece, 11521
Status
Study Complete
Location
GSK Investigational Site
Athens, Greece, 11522
Status
Study Complete
Location
GSK Investigational Site
Athens, Greece, 11528
Status
Study Complete
Location
GSK Investigational Site
BUCHAREST, Romania
Status
Study Complete
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Study documents

Clinical study report
Available language(s): English

If you wish to request for full study report, please contact - [email protected]

Results overview

Refer to study documents

Recruitment status
Study complete
Actual primary completion date
2008-29-07
Actual study completion date
2008-29-07

Plain language summaries

Not applicable. GSK’s transparency policy provides for Plain Language Summaries for Interventional studies.

Additional information about the trial

Not applicable
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