Oxis 9mcg Turbuhaler Clinical Experience Investigation

NCT01749462 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 398

Last updated 2016-02-10

No results posted yet for this study

Summary

The purpose of the investigation is to confirm the ADR development and the contributing factors possibly having an impact on the safety under the post-marketing actual use of Oxis 9 mcg Turbuhaler.

Conditions

Sponsors & Collaborators

Principal Investigators

  • Shigeru Yoshida, MD · Astrazeneca KK

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2015-07-31
Completion
2015-07-31

Countries

  • Japan

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01749462 on ClinicalTrials.gov