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Modafinil for the treatment of fatigue in lung cancer: a pilot study

Modafinil for the treatment of fatigue in lung cancer: a pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN82265570
Enrollment
20
Registered
2006-04-24
Start date
2006-04-26
Completion date
Unknown
Last updated
2022-11-07

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

Conditions

Non small cell lung cancer Cancer Non small cell lung cancer

Interventions

Modafinil 100 mg daily for one week, increasing to 200 mg daily for one week

Sponsors

Cambridge University Hospitals NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Histologically or cytologically confirmed non-small cell lung cancer (NSCLC) 2. A fatigue score of four using bimodal scoring in the Chalder fatigue scale 3. World Health Organisation (WHO) performance status of 0-3 4. Ability to give informed consent to participate

Exclusion criteria

Exclusion criteria: 1. Received radiotherapy or chemotherapy within the last four weeks 2. Commenced on antidepressants or steroids (corticosteroids and progestational steroids) within the last two weeks 3. Received blood transfusion within the last two weeks 4. Potentially fertile women of child-bearing age 5. Uncontrolled moderate to severe hypertension, arrhythmia 6. Previous adverse reaction to modafinil or other central nervous system (CNS) stimulant 7. Current active involvement in another clinical trial

Design outcomes

Primary

MeasureTime frame
Change in fatigue

Secondary

MeasureTime frame
Change in sleepiness and depression levels

Countries

England, United Kingdom

Outcome results

None listed

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