Patient Controlled Administration of Methylphenidate for Cancer Related Fatigue - PRN Methylphenidate

PHASE1CompletedINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

August 1, 2002

Primary Completion Date

December 28, 2021

Study Completion Date

December 28, 2021

Conditions
Fatigue
Interventions
DRUG

Methylphenidate

5 mg tablet by mouth as needed every 2 hours for participant described significant fatigue. Participants to take a maximum of 20 mg/day, for total of 28 tablets for 7 days.

BEHAVIORAL

Fatigue Evaluations

Participants to have evaluation of their fatigue, ability to sleep, and will answer a set of general symptom questions at baseline visit, daily while on study drug, and on seventh day of treatment.

Trial Locations (1)

77030

University of Texas MD Anderson Cancer Center, Houston

All Listed Sponsors
lead

M.D. Anderson Cancer Center

OTHER

NCT02361125 - Patient Controlled Administration of Methylphenidate for Cancer Related Fatigue - PRN Methylphenidate | Biotech Hunter | Biotech Hunter