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Trials / Completed

CompletedNCT01045603

Instanyl® Non-Interventional Study

A 3 Month Observational Prospective Patient Cohort Study of the Treatment of Breakthrough Pain in Cancer Patients With Instanyl®

Status
Completed
Phase
Study type
Observational
Enrollment
309 (actual)
Sponsor
Takeda · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to describe the use of Instanyl® (Intranasal fentanyl spray) in the treatment of breakthrough pain (BTP) in cancer patients by success of dose titration and distribution of dose strength. Data will be collected at three different time points over a 3 month period.

Conditions

Timeline

Start date
2009-12-01
Primary completion
2012-04-01
Completion
2012-04-01
First posted
2010-01-11
Last updated
2012-10-29

Locations

65 sites across 7 countries: Denmark, France, Greece, Ireland, Norway, Sweden, United Kingdom

Source: ClinicalTrials.gov record NCT01045603. Inclusion in this directory is not an endorsement.

Instanyl® Non-Interventional Study (NCT01045603) · Clinical Trials Directory