Fatigue and Symptom Burden in Febrile Neutropenia
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|ClinicalTrials.gov Identifier: NCT00503854|
Recruitment Status : Active, not recruiting
First Posted : July 19, 2007
Last Update Posted : February 22, 2018
- To determine whether fatigue improves as patients are treated for febrile neutropenia (Day #1, Day #2 and Day #6).
- To identify clinical factors associated in cancer patients with low risk for outpatient treatment of febrile neutropenia on either outpatient febrile neutropenia treatment pathway presenting with moderate to severe fatigue. Moderate fatigue is defined as a score of 4 through 6 on the Brief Fatigue Inventory and severe fatigue is defined as a score of 7 through 10 on the Brief Fatigue Inventory.
- To describe demographic information in cancer patients with low risk for outpatient treatment of febrile neutropenia and fatigue while enrolled in either of two outpatient febrile neutropenia treatment pathways.
|Condition or disease||Intervention/treatment|
|Solid Tumors Febrile Neutropenia||Behavioral: Questionnaire|
|Study Type :||Observational|
|Estimated Enrollment :||70 participants|
|Official Title:||Fatigue and Symptom Burden in Febrile Neutropenia|
|Actual Study Start Date :||May 2007|
|Estimated Primary Completion Date :||May 2019|
|Estimated Study Completion Date :||May 2020|
|Fatigue and Fever Assessment||
Questionnaires taking about 15 to 30 minutes total.
Other Name: Survey
- Improvement in mean fatigue level from study day 1 to day 6 [ Time Frame: 6 Days (Baseline to Day 6) ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00503854
|United States, Texas|
|University of Texas MD Anderson Cancer Center|
|Houston, Texas, United States, 77030|
|Principal Investigator:||Carmen Escalante, MD||M.D. Anderson Cancer Center|