Dexamethasone for Treatment of Radiation-related Fatigue in Patients Receiving RT for Head-neck and Lung Cancer
Stopped early · Phase 2 · Has a placebo group
Conditions studied: Head and Neck Cancer, Non-small Cell Lung Cancer
In brief
This study will look at how dexamethasone and placebo influence radiation fatigue, quality of life and number of treatment days missed during radiation therapy or radiation therapy and chemotherapy for cancer.
Key facts
- Study ID
- NCT02410382
- Run by
- University of Arizona
- People needed
- 79
- Starts
- 2014-08-27
- Expected to finish
- 2018-02-16
- Last updated by the study team
- 2019-05-14
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- confirmation of head \& neck cancer (stage I-IV) or non-small cell lung cancer (stage II \& III)
- Undergoing treatment with either radiation alone or in combination with chemotherapy
- Normal cognition and willingness to complete fatigue and quality of life forms, patient observation form, and pill diary
You may not qualify if…
- Hypersensitivity to dexamethasone or corticosteroids or Equal sugar substitute
- Corticosteroid within the past 30 days prior to study enrollment for greater than one week duration
- Planned Stereotactic Body Radiation Therapy (SBRT)
- Active psychosis
- Current pregnancy
- Active peptic ulcer disease or evidence of gastrointestinal bleed
- Current active tuberculosis or systemic fungal infection
- Previous diagnosis of diabetes mellitus
- Acute febrile illness
- Known human immunodeficiency virus or acquired immunodeficiency syndrome
- Major surgery within two weeks of study enrollment of which the patient has not recovered
- Psychostimulant use in the past 30 days prior to registration
- History of phenylketonuria (PKU)
Where it is running
- University of Arizona — Tucson, Arizona, United States
Full record on ClinicalTrials.gov
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