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Nasal Fentanyl for Chronic Cancer Pain

WithdrawnPhase 3NCT01906073
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Today, patients with cancer pain in need of opioids for moderate to severe pain get long-acting morphine twice a day and morphine tablets taken on demand in addition. This procedure might be based on the assumption that cancer pain is persistent, although the evidence to support whether this assumption applies to all cancer patients is lacking. Some cancer patients might not need a fixed dose of long-acting morphine. Because of rapid pain relief, the new fentanyl drugs open for the possibility to take an opioid on demand when pain occurs. A pilot study where 10 patients with cancer pain were treated with a rapid-acting fentanyl nasal spray taken on demand, showed that this treatment was apparently feasible and safe for these patients. This approach is studied further in NFCP-II. The participants will be treated with rapid-acting fentanyl nasal spray and long-acting morphine in a crossover study. The primary outcome will be patient satisfaction. The study will consist of a test dose of nasal fentanyl, a dose-finding phase and a treatment phase with either nasal fentanyl taken on demand or slow-released morphine taken twice a day. After 10 days of treatment there is a crossover and the opposite drug is used for the same participant. Morphine tablets can be taken on demand in all phases of the study. The participants will meet the investigator at inclusion, at the crossover and at the end of treatment. During the study, a diary is filled in by the participants every morning. Questions about pain and side effects are answered. Satisfaction is measured at the crossover and at end of treatment while preference is measured at the end of treatment.

Study details

Official title
An Open Label, Cross-over, Randomized Controlled Multicenter Phase III Study Comparing Standard Oral SR-morphine by the Clock Medications With Self-controlled Nasal Fentanyl for Chronic Cancer Pain Requiring Opioids
Conditions
Interventions
  • Drug: intranasal fentanyl spray
  • Drug: slow release morphine
Sponsor
Norwegian University of Science and Technology
Collaborators
St. Olavs Hospital; Fondazione IRCCS Istituto Nazionale dei Tumori, Milano; L'Hospitalet de Llobregat; University Hospital, Bonn; Cantonal Hospital of St. Gallen; Maastricht University Medical Center; Flinders University
Start date
2017-01
Primary completion
2020-12
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Total sites listed
0

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Cancer disease 2. Adult (older than 18 years) 3. Cancer-related pain \> 4 on an 11 point Numerical Rating Scale (NRS) 4. In the need of opioids (step II or III) 5. Able to use nasal drugs. 6. Life expectancy of \> 6 months 7. Karnofsky status \> = 60 8. Women of child bearing potential must use adequate contraception 9. Informed consent given according to applicable requirements before any trial-related activities. Exclusion Criteria: 1. Use of opioids for moderate and severe pain 2. History of substance abuse.\* 3. Pathological conditions of the nasal cavity as contraindication to nasal fentanyl 4. Renal- or liver- failure, defined as creatinin \> 150 and alanine-amino transferase (ALAT) \> x 1.5 reference value 5. Sleep apnoea syndrome, severe chronic obstructive lung disease or illnesses leading to severe respiratory depression. 6. Psychiatric disease 7. Neurological disease giving dizziness or sedation 8. Cognitive impairment which makes the patient unable to complete questionnaires or not able to comply with the study procedures. 9. Previous or ongoing facial radiotherapy 10. Recurrent nose bleeding 11. Known hypersensitivity to the active substances or excipients of the study drugs 12. Pregnant or breastfeeding women 13. Treated with monoamine oxidase (MAO) inhibitor within the last 14 days

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01906073