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WithdrawnNCT01839552

An Assessment of the Ability of Fentanyl Citrate Nasal Spray to Manage Breakthrough Pain in Cancer Patients.

An Assessment of the Ability of Fentanyl Citrate Nasal Spray to Manage Breakthrough Pain in Cancer Patients Without a Timely Response to Their Short-acting Opioids.

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
University of Louisville · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Lazanda is a prescription nasal spray medicine that contains the medicine fentanyl. It is used to manage breakthrough pain in adults with cancer who are already routinely taking other opioid pain medicines around-the-clock for cancer pain. Lazanda is started only after taking other opioid pain medicines and the patient's body has become used to them (opioid tolerant). The purpose of this study is to assess the ability of Lazanda to control pain during an episode of breakthrough pain in cancer patients.

Conditions

Interventions

TypeNameDescription
DRUGFentanyl Citrate Nasal Spray (FCNS)

Timeline

Start date
2014-10-01
Primary completion
2017-04-01
Completion
2018-04-01
First posted
2013-04-25
Last updated
2018-03-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01839552. Inclusion in this directory is not an endorsement.

An Assessment of the Ability of Fentanyl Citrate Nasal Spray to Manage Breakthrough Pain in Cancer Patients. (NCT01839552) · Clinical Trials Directory