Morphine or Fentanyl for Refractory Dyspnea in COPD (MoreFoRCOPD)
Primary Purpose
COPD
Status
Recruiting
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
Fentanyl
Morphine Retard
Placebo patch
Placebo oral capsule
Sponsored by
About this trial
This is an interventional treatment trial for COPD focused on measuring COPD, Refractory Dyspnea, Morphine, Fentanyl
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 ≥ 3.
- 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
Sites / Locations
- Wilhelmina Ziekenhuis AssenRecruiting
- Ommelander Ziekenhuis GroningenRecruiting
- Elkerliek ZiekenhuisRecruiting
- Noordwest Ziekenhuisgroep AlkmaarRecruiting
- Rode Kruis ZiekenhuisRecruiting
- Spaarne GasthuisRecruiting
- Medisch Spectrum TwenteRecruiting
- Isala KliniekenRecruiting
- Ikazia ZiekenhuisRecruiting
- University Medical Center GroningenRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Experimental
Placebo Comparator
Arm Label
Morphine capsules and Placebo patch
Placebo capsules and Fentanyl patch
Placebo capsules and Placebo patch
Arm Description
Morphine retard 10 mg twice daily Placebo patch, change every three days.
Placebo capsules twice daily Fentanyl patch 12 mcg/hr, change every three days
Placebo capsules twice daily Placebo patch, change every three days
Outcomes
Primary Outcome Measures
Change in dyspnea sensation
Change in dyspnea sensation measured on a Numeric Rating Scale from 0 to 10. A lower score represents a better outcome.
Secondary Outcome Measures
Change in CCQ (HR-QoL)
Change in HR-QoL measured with the Clinical COPD Questionnaire. Scores range from 0 to 6. Lower values represent a better outcome.
Change in CRQ (HR-QoL)
Change in HR-QoL measured with Chronic Respiratory Disease Questionnare. Scores range from 1 to 7. A higher score represents a better outcome.
Change in CRQ mastery (HR-QoL)
Change in HR-QoL measured with Chronic Respiratory Disease Questionnare, domain Mastery. Scores range from 1 to 7. A higher score represents a better outcome.
Change on the HADS-A questionnaire (Anxiety)
Change on the Hospital Anxiety and Depression Scale-anxiety subscale. Scores range from 0 to 21. A lower score represents a better outcome.
Side effects
Reported spontaneously in a daily patient diary and specifically, both open and named side effects at planned visits.
Hypercapnia
Change in pCO2 in capillary blood gas analysis
Sleep quality
Change on a Numeric Rating Scale from 0 to 10. A lower score represents a better outcome.
Continued opioid use
Asked three months after the end of the treatment period
Full Information
NCT ID
NCT03834363
First Posted
January 11, 2019
Last Updated
November 16, 2022
Sponsor
Huib A.M. Kerstjens
Collaborators
Dutch Foundation for Asthma Prevention, Innovatiefonds Zorgverzekeraars
1. Study Identification
Unique Protocol Identification Number
NCT03834363
Brief Title
Morphine or Fentanyl for Refractory Dyspnea in COPD
Acronym
MoreFoRCOPD
Official Title
Morphine or Fentanyl for Refractory Dyspnea in COPD
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 15, 2019 (Actual)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Huib A.M. Kerstjens
Collaborators
Dutch Foundation for Asthma Prevention, Innovatiefonds Zorgverzekeraars
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COPD
Keywords
COPD, Refractory Dyspnea, Morphine, Fentanyl
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Model Description
Crossover, double blind, double dummy Randomized Controlled Trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
For both morphine retard capsules as fentanyl patches there is a placebo available. Participants will be treated in each period with both tablets and a patch. (morphine capsules+placebo patch, placebo capsules+fentanyl patch, placebo capsules+ placebo patch.)
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Morphine capsules and Placebo patch
Arm Type
Active Comparator
Arm Description
Morphine retard 10 mg twice daily Placebo patch, change every three days.
Arm Title
Placebo capsules and Fentanyl patch
Arm Type
Experimental
Arm Description
Placebo capsules twice daily Fentanyl patch 12 mcg/hr, change every three days
Arm Title
Placebo capsules and Placebo patch
Arm Type
Placebo Comparator
Arm Description
Placebo capsules twice daily Placebo patch, change every three days
Intervention Type
Drug
Intervention Name(s)
Fentanyl
Other Intervention Name(s)
Fentanyl Matrix
Intervention Description
Fentanylpatch 12 mcg/hr, change patch every three days.
Intervention Type
Drug
Intervention Name(s)
Morphine Retard
Other Intervention Name(s)
Morphine
Intervention Description
Morphine retard capsules 10 mg bid.
Intervention Type
Drug
Intervention Name(s)
Placebo patch
Intervention Description
Placebo patch, change patch every three days.
Intervention Type
Drug
Intervention Name(s)
Placebo oral capsule
Intervention Description
Placebo oral capsule bid
Primary Outcome Measure Information:
Title
Change in dyspnea sensation
Description
Change in dyspnea sensation measured on a Numeric Rating Scale from 0 to 10. A lower score represents a better outcome.
Time Frame
Daily during the six week treatment period
Secondary Outcome Measure Information:
Title
Change in CCQ (HR-QoL)
Description
Change in HR-QoL measured with the Clinical COPD Questionnaire. Scores range from 0 to 6. Lower values represent a better outcome.
Time Frame
Daily during the six week treatment period
Title
Change in CRQ (HR-QoL)
Description
Change in HR-QoL measured with Chronic Respiratory Disease Questionnare. Scores range from 1 to 7. A higher score represents a better outcome.
Time Frame
4 times during the six week treatment period: baseline, 2 weeks, 4 weeks, 6 weeks.
Title
Change in CRQ mastery (HR-QoL)
Description
Change in HR-QoL measured with Chronic Respiratory Disease Questionnare, domain Mastery. Scores range from 1 to 7. A higher score represents a better outcome.
Time Frame
4 times during the six week treatment period: baseline, 2 weeks, 4 weeks, 6 weeks.
Title
Change on the HADS-A questionnaire (Anxiety)
Description
Change on the Hospital Anxiety and Depression Scale-anxiety subscale. Scores range from 0 to 21. A lower score represents a better outcome.
Time Frame
4 times during the six week treatment period: baseline, 2 weeks, 4 weeks, 6 weeks.
Title
Side effects
Description
Reported spontaneously in a daily patient diary and specifically, both open and named side effects at planned visits.
Time Frame
Daily during the six week treatment period
Title
Hypercapnia
Description
Change in pCO2 in capillary blood gas analysis
Time Frame
4 times during the six week treatment period: baseline, 2 weeks, 4 weeks, 6 weeks.
Title
Sleep quality
Description
Change on a Numeric Rating Scale from 0 to 10. A lower score represents a better outcome.
Time Frame
Daily during the six week treatment period
Title
Continued opioid use
Description
Asked three months after the end of the treatment period
Time Frame
Once, three months after the end of the treatment period
Other Pre-specified Outcome Measures:
Title
Survival
Description
Measured one week after the end of the treatment period
Time Frame
One week after the end of the treatment period, which is 7 weeks after start of the study.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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 ≥ 3.
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marlies van Dijk, MD
Phone
+31503612357
Email
m.van.dijk05@umcg.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Huib AM Kerstjens, MD PhD
Phone
+31503610280
Email
h.a.m.kerstjens@umcg.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Huib AM Kerstjens, MD PhD
Organizational Affiliation
University Medical Center Groningen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wilhelmina Ziekenhuis Assen
City
Assen
State/Province
Drenthe
ZIP/Postal Code
9401 RK
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sander De Hosson, MD
First Name & Middle Initial & Last Name & Degree
Sander De Hosson, MD
Facility Name
Ommelander Ziekenhuis Groningen
City
Scheemda
State/Province
Groningen
ZIP/Postal Code
9676 BJ
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jan Willem De Jong, MD PhD
Facility Name
Elkerliek Ziekenhuis
City
Helmond
State/Province
Noord-Brabant
ZIP/Postal Code
5707 HA
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wai Yee Lam, MD PhD
First Name & Middle Initial & Last Name & Degree
Wai Yee Lam, MD PhD
Facility Name
Noordwest Ziekenhuisgroep Alkmaar
City
Alkmaar
State/Province
Noord-Holland
ZIP/Postal Code
1815 JD
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Liesbeth Peters, MD
First Name & Middle Initial & Last Name & Degree
Liesbeth Peters, MD
Facility Name
Rode Kruis Ziekenhuis
City
Beverwijk
State/Province
Noord-Holland
ZIP/Postal Code
1942 LE
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karin Pool, MD
First Name & Middle Initial & Last Name & Degree
Karin Pool, MD
Facility Name
Spaarne Gasthuis
City
Haarlem
State/Province
Noord-Holland
ZIP/Postal Code
2035 RC
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kris Mooren, MD
First Name & Middle Initial & Last Name & Degree
Kris Mooren, MD
Facility Name
Medisch Spectrum Twente
City
Enschede
State/Province
Overijssel
ZIP/Postal Code
7512 KZ
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wendy Van Beurden, MD
First Name & Middle Initial & Last Name & Degree
Wendy van Beurden, MD
Facility Name
Isala Klinieken
City
Zwolle
State/Province
Overijssel
ZIP/Postal Code
8025 AB
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jan Willem Van den Berg, MD PhD
First Name & Middle Initial & Last Name & Degree
Jan WIllem Van den Berg, MD PhD
Facility Name
Ikazia Ziekenhuis
City
Rotterdam
State/Province
Zuid-Holland
ZIP/Postal Code
3083 AN
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Roxane Heller-Baan, MD
First Name & Middle Initial & Last Name & Degree
Roxane Heller-Baan, MD
Facility Name
University Medical Center Groningen
City
Groningen
ZIP/Postal Code
9713GZ
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Huib A.M. Kerstjens, MD PhD
First Name & Middle Initial & Last Name & Degree
Huib A.M. Kerstjens, MD PhD
First Name & Middle Initial & Last Name & Degree
Marlies van Dijk, MD
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Upon request
IPD Sharing Time Frame
After publication of results Unlimited
IPD Sharing Access Criteria
Clear description of goals for asking
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Results Reference
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Citation
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Results Reference
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Citation
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Citation
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Morphine or Fentanyl for Refractory Dyspnea in COPD
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