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Comparison of bupropion, fluoxetine, and methylphenidate in cancer-related fatigue

Comparison of the effectiveness of bupropion, fluoxetine, and methylphenidate in improving cancer-related fatigue

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180623040193N3
Enrollment
60
Registered
2020-08-11
Start date
2020-08-22
Completion date
Unknown
Last updated
2020-09-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer-related fatigue.

Interventions

Intervention 1: Intervention group: Fluoxetine 20 mg/d (Exir pharmaceutics, Iran) for the first 5 days then twice a day for the rest of the first month. In the second month, depending on the patient's

Sponsors

Shahre-kord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Definite diagnosis of cancer from at least 2 month ago Patients are undergoing outpatient chemotherapy Lack of metastasis Lack of any chronic cardiac or respiratory diseases or diabetes mellitus Lack of severe bone pain and balance problem Hemoglobin= 10 Ability to read and write Not receiving any type of treatment (drug or psychotherapy) for fatigue in the past Not having leukemia Lack of past history of any major psychiatric illnesses for which patient was hospitalized or medicated

Exclusion criteria

Exclusion criteria: Acute respiratory, cardiac or infectious diseases Hemoglobin<10 Uncontrolled hypothyroidism

Design outcomes

Primary

MeasureTime frame
Fatigue score in Cancer Fatigue scale and Fatigue Visual Analogue scale. Timepoint: Before intervention, 1 month and 2 months after pharmacotherapy. Method of measurement: Cancer Fatigue scale, Fatigue Visual Analogue scale.

Secondary

MeasureTime frame
The Quality of life score in European Organization for Research and treatment of cancer quality of life questionnaire. Timepoint: Before intervention, 1 month and 2 months after pharmacotherapy. Method of measurement: European Organization for Research and treatment of cancer quality of life questionnaire version 3.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Zarean

Shahre-kord University of Medical Sciences

ezarean@gmail.com+98 38 3222 0016

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026