Cancer breathlessness study: can opioids help you walk easier?
NCT ID NCT04188418
First seen Jun 27, 2026 · Last updated Aug 12, 2026 · Updated 2 times
Summary
This study tests if fast-acting opioids (fentanyl or morphine) can reduce shortness of breath during or after walking in 150 cancer patients who already take strong painkillers. Participants will take the drug or a placebo before a short walk test, and researchers will measure changes in their breathing difficulty. The goal is to find a new way to improve daily comfort and activity for people with advanced cancer.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2020
- Expected to finish
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Aug 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Diagnosis of cancer with evidence of active disease 2. Dyspnea on exertion with an average intensity level ≥4/10 on a modified Borg scale 3. Outpatient at participating centers 4. Ambulatory and able to walk, with or without walking aid 5. On strong opioids with morphine equivalent daily dose (MEDD) of 60-400 mg for ≥1 wk (i.e. at least 4 out of 7 days), with stable (i.e. ±30%) regular dose over the last 3 d 6. Karnofsky performance status ≥40% 7. Age ≥18 yrs 8. Able to complete study assessments 9. Able to speak English or Spanish 10. Reside within 65 miles of participating centers or expected to visit MD Anderson in person at least once a month Exclusion Criteria: 1. Dyspnea at rest ≥7/10 on modified Borg scale at enrollment 2. Supplemental oxygen requirement \>6 L/min 3. Delirium (i.e. Memorial Delirium Assessment Scale ≥13) 4. History of unstable angina or myocardial infarction 1 mo prior to enrollment 5. Hemodynamic instability requiring hospitalization 6. History of substance use disorder or abnormal urinary drug screen within the past year, or at risk of opioid abuse as determined by Screener and Opioid Assessment for Patients with Pain (SOAPP14) ≥7 7. History of or known allergy to fentanyl or morphine sulfate 8. Using scheduled benzodiazepines at the time of enrollment and cannot stop during the study 9. Severe anemia (Hb \<7 g/L) if documented in the last month and not corrected prior to study enrollment\* 10. Bilirubin ≥5x upper limit of normal if documented in the last month and not lowered to \<5x normal prior to enrollment\* 11. Diagnosis of acute pulmonary embolism within past 2 wks 12. Diagnosis of pulmonary hypertension 13. Diagnosis of malignant pleural effusion with therapeutic thoracentesis expected in the next 2 wks 14. Currently pregnant or breastfeeding 15. Unwilling to provide informed consent
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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M D Anderson Cancer Center
Houston, Texas, 77030, United States
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