Overview

The Use of Intranasal Fentanyl for the Treatment of Incident Dyspnea in Congestive Heart Failure: A Prospective Trial

Status:
Completed
Trial end date:
2017-09-15
Target enrollment:
0
Participant gender:
All
Summary
Study Objective The primary object of this study is to investigate the safety and effectiveness of fentanyl on the management of incident dyspnea. Study Design The study design will be a cross over study with a minimum of a one hour wash out period.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
St. Boniface General Hospital Research Centre
St. Boniface Hospital
Treatments:
Fentanyl
Criteria
Inclusion Criteria:

- Patients must be experiencing activity-induced incident dyspnea without reversible
causes. They would have controlled background dyspnea without opioids.

- Patients must be physically able to safely ambulate in order to complete the 6MWT (may
have mobility devices and may use supplement oxygen prescribed pre-study).

Exclusion Criteria:

- Patients who are unable to perform the 6MWT for any reason or have contraindications
to performing the 6MWT

- Patients that have anatomical pathologies that would make intranasal administration
impossible

- Patients with known allergies/sensitivities to fentanyl/sufentanil