Comparison of Nasal Fentanyl and Oral Transmucosal Fentanyl (Actiq) in Cancer Breakthrough Pain (FT-019-IM)

• Status: Completed
• Trial end date: 2009-10-01
• Target enrollment: 0
• Participant gender: All

Summary

Primary:

• To compare the efficacy of nasal fentanyl (NF) to oral transmucosal fentanyl (Actiq®) (hereafter Actiq) in the management of breakthrough pain in cancer patients.

Secondary:

• To compare patients' general impression and preference of NF and Actiq

• To explore the relationship between NF doses and dose of current opioid for breakthrough pain (BTP) and the relationship between dose of NF and of background opioid

• To assess safety and tolerability of NF

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Nycomed
• Treatments: Fentanyl

Criteria

Inclusion Criteria:

• Adult in- or out patient with cancer and breakthrough pain; using a stable, chronic opioid treatment for background pain.

• Minimum three BTP episodes per week and maximum four per day. Life expectancy of at least three months.

• Chemotherapy and palliative radiotherapy (except facial radiotherapy) are allowed.

• Randomisation in previous studies with NF, i.e. FT-016-IM, FT-017-IM or FT-018-IM, is not allowed.

• Previous use of Actiq is accepted.