drugset / Trial / NCT01980498

PEctin Rapid Fentanyl Efficacy Clinical Trial For pAin at Swallowing Undergoing radioTherapy

NCT01980498

RandomizedParallel-groupOpen-labelPrevention

Summary

The primary objective of the present phase IIIb study is to assess the efficacy of FPNS compared with Physician Choice-Usual Care (PC-UC) in the reduction of swallowing predictable BTP in head and neck cancer patients undergoing radiotherapy with or without chemotherapy.

Timeline

Start
2014-09
Primary completion
2015-09
Completion
2015-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Fentanyl Other / unclassified 800 ug Intranasal

Indications

No indication recorded.