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Clinical Trials/NCT03834363
NCT03834363
Completed
Phase 4

Morphine or Fentanyl for Refractory Dyspnea in COPD

Huib A.M. Kerstjens10 sites in 1 country59 target enrollmentNovember 15, 2019

Overview

Phase
Phase 4
Intervention
Morphine Retard
Conditions
COPD
Sponsor
Huib A.M. Kerstjens
Enrollment
59
Locations
10
Primary Endpoint
Change in dyspnea sensation
Status
Completed
Last Updated
11 months ago

Overview

Brief Summary

Rationale: The most important complaint in severe COPD is dyspnea which is associated with a diminished exercise tolerance, reduced quality of life and can lead to anxiety and depression. If dyspnea continues to exist despite optimal therapy it is called refractory dyspnea. There is evidence that morphine is effective and can safely be prescribed for treating refractory dyspnea.

However, a Dutch study recently showed that few pulmonologists actually prescribe opioids for this indication. The main reasons for this are concerns about side effects and respiratory insufficiency as well as negative emotions for the patient and families at the thought of using morphine.

Most studies investigating opioids for treatment of dyspnea are conducted with morphine tablets, and only a part of these patients suffered from COPD. To our knowledge there has not been a randomized controlled trial investigating fentanyl patches for refractory dyspnea in COPD patients. However, studies comparing fentanyl and morphine in pain management show that patients may prefer fentanyl patches and have less problems with obstipation.

Objective: There are three main objectives for this study.

First, the investigators will investigate the following hypothesis: Both fentanyl and morphine provide a reduction of dyspnea which is better than placebo. Fentanyl has less side effects than morphine.

Secondly, with this Dutch multi-center study the investigators would like to enlarge the evidence base and contribute to the experience with opioids for refractory dyspnea in COPD thereby greatly facilitating its implementation in the Netherlands.

Finally, the investigators will develop and evaluate educational material about opioid use for dyspnea in COPD.

Study design: This is a multi-center double blind, double-dummy cross-over randomized placebo-controlled trial with three study arms. A total of 60 COPD patients will be included in this study.

Participants will be treated sequentially with three combinations of medication and/or placebo medication in a random order. They will receive either a Fentanyl patch in combination with placebo tablets, a placebo patch with Morphine Slow release tablets or a placebo patch with placebo tablets. Main study parameters/endpoints: The primary endpoint is change in dyspnea sensation Secondary endpoints are change in HR-QoL, anxiety, sleep quality, hypercapnia and the number and seriousness of side effect.

Registry
clinicaltrials.gov
Start Date
November 15, 2019
End Date
August 24, 2024
Last Updated
11 months ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Huib A.M. Kerstjens
Responsible Party
Sponsor Investigator
Principal Investigator

Huib A.M. Kerstjens

Full professor pulmonology, head of department pulmonology and tuberculosis, principal investigator.

University Medical Center Groningen

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 40 years.
  • Read, understood and signed the Informed Consent form.
  • COPD GOLD class III or IV, according to GOLD criteria (Post-bronchodilation FEV/FVC \<70% and FEV1 \< 50%pred.
  • Complaints of refractory dyspnea as established by patient and doctor.
  • mMRC score ≥
  • Life expectancy of ≥ 2 months.
  • Optimized standard therapy according to Dutch LAN guideline for diagnosis and treatment of COPD.

Exclusion Criteria

  • Other severe disease with chronic pain or chronic dyspnea (a non substantial component of left sided heart failure is acceptable).
  • Current use of opioids for whatever indication.
  • Allergy / intolerance for opioids
  • Psychiatric disease, not related to severe COPD.
  • Exacerbation of COPD 8 weeks prior to inclusion or between screening and randomization.
  • Problematic (leading to medical help or social problems) substance abuse during the last five years.
  • Active malignancy, with the exception of planocellular or basal cell carcinoma of the skin.
  • eGFR \<15 ml/min

Arms & Interventions

Morphine capsules and Placebo patch

Morphine retard 10 mg twice daily Placebo patch, change every three days.

Intervention: Morphine Retard

Morphine capsules and Placebo patch

Morphine retard 10 mg twice daily Placebo patch, change every three days.

Intervention: Placebo patch

Placebo capsules and Fentanyl patch

Placebo capsules twice daily Fentanyl patch 12 mcg/hr, change every three days

Intervention: Fentanyl

Placebo capsules and Fentanyl patch

Placebo capsules twice daily Fentanyl patch 12 mcg/hr, change every three days

Intervention: Placebo oral capsule

Placebo capsules and Placebo patch

Placebo capsules twice daily Placebo patch, change every three days

Intervention: Placebo patch

Placebo capsules and Placebo patch

Placebo capsules twice daily Placebo patch, change every three days

Intervention: Placebo oral capsule

Outcomes

Primary Outcomes

Change in dyspnea sensation

Time Frame: Daily during the six week treatment period

Change in dyspnea sensation measured on a Numeric Rating Scale from 0 to 10. A lower score represents a better outcome.

Secondary Outcomes

  • Hypercapnia(4 times during the six week treatment period: baseline, 2 weeks, 4 weeks, 6 weeks.)
  • Change in CCQ (HR-QoL)(Daily during the six week treatment period)
  • Change in CRQ (HR-QoL)(4 times during the six week treatment period: baseline, 2 weeks, 4 weeks, 6 weeks.)
  • Change on the HADS-A questionnaire (Anxiety)(4 times during the six week treatment period: baseline, 2 weeks, 4 weeks, 6 weeks.)
  • Sleep quality(Daily during the six week treatment period)
  • Change in CRQ mastery (HR-QoL)(4 times during the six week treatment period: baseline, 2 weeks, 4 weeks, 6 weeks.)
  • Side effects(Daily during the six week treatment period)
  • Continued opioid use(Once, three months after the end of the treatment period)

Study Sites (10)

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