ROTATEQ™ Post-Marketing Surveillance in the Philippines

NCT ID: NCT01357174

Last Updated: 2015-10-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Total Enrollment

915 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-10-31

Study Completion Date

2010-09-30

Brief Summary

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This study will collect demographic and safety information on the use of ROTATEQ™ in the Philippines.

Detailed Description

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Conditions

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Rotavirus Infections Gastroenteritis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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All Participants

Infants who were vaccinated with ROTATEQ™

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Received ROTATEQ™
Minimum Eligible Age

6 Weeks

Maximum Eligible Age

12 Weeks

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Merck Sharp & Dohme LLC

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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V260-046

Identifier Type: -

Identifier Source: org_study_id