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Clinical Trial to Evaluate Short-term Efficacy of Palliative Methylphenidate in Asthenia in Advanced Cancer Patients

Phase 3
Terminated
Conditions
Asthenia
Interventions
Registration Number
NCT01773837
Lead Sponsor
Clinica Universidad de Navarra, Universidad de Navarra
Brief Summary

Fatigue is the most prevalent symptom in advanced cancer patients, interfering functional capacity, social relations, wellbeing, and quality of life. Methylphenidate is a central nervous system stimulant that has traditionally been used in cancer patients to manage depression, opioid-induced sedation, hypoactive delirium due to multiorgan failure, and cognitive disorder associated with brain tumors. Although there is evidence from prospective studies of the efficacy of this drug in cancer-related fatigue, the only one randomised clinical trials gave non-conclusive results. In order to define the real efficacy of methylphenidate in this setting, the investigators designed a new clinical trial comparing methylphenidate and placebo in cancer-related fatigue, assessed both by the verbal numeric scale (VNS) included in the Edmonton Symptom Assessment System (ESAS) and the subscale for fatigue of the Functional Assessment of Cancer Therapy (FACT-F). The investigators will include 122 advanced cancer patients with fatigue ≥ 5/10 (VNS, from 0 to 10) and hemoglobin ≥ 9 g/dl. Patients will be randomized to methylphenidate or placebo. Doses will be adapted to response within a range from 10 mg at morning time and 5 at noon, to 25 mg/day. Assessment of response will be performed on day 3 and day 6 with ESAS and FACT-F. Drug-induced adverse events will be checked. The VNS of fatigue on day 6 will be consider the primary endpoint.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Advanced cancer; including metastatic, locally advanced or relapsed not amenable for curative treatment.
  • Mini.mental status examination results within normal limits.
  • Informed consent.
  • Estimated life expectancy of at least one month.
  • Hemoglobin >= 9 g/dl.
  • Asthenia >= 5 (0-10; numeric verbal scale).
Exclusion Criteria
  • History of psychosis.
  • Structured suicidal ideation.
  • Severe anxiety.
  • Severe renal, hepatic or cardiac (arrythmia, hypertension, ischemic heart disease) failure.
  • Simultaneous treatment with drugs that may interact with methylphenidate as: coumarinics, anticonvulsivants (phenobarbital, phenitoin, primidone), phenylbutazone, inhibitors of mono-amine-oxidase, guanethidine.
  • History of glaucoma.
  • Hyperthyroidism.
  • History of hypersensibility to methylphenidate.
  • Clinical suspicion of: infection, hypercalcemia, hypothyroidism or renal failure.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
placeboplacebothe same number of pills (p.o.) than methylphenidate for six days
methylphenidatemethylphenidatemethylphenidate (pill) p.o. 15 to 25 mg daily for six days
Primary Outcome Measures
NameTimeMethod
Intensity of asthenia assessed with the verbal numeric scale (VNS) included on the Edmonton Symptom Assessment System (ESAS)After six days of therapy

We are looking for a difference between goups (methylphenidate versus placebo) of 1.5 (numeric rating scale: o to 10)

Secondary Outcome Measures
NameTimeMethod
Intensity of other symptoms assessed with the Edmonton Symptom Assessment System (ESAS)After three and six days of treatment
Intensity of asthenia assessed with the verbal numeric scale (VNS) included on the Edmonton Symptom Assessment System (ESAS) and the subscale for fatigue of the Functional Assessment of Cancer Therapy (FACT-F).After three and six days of therapy
Intensity of asthenia assessed with the subscale for fatigue of the Functional Assessment of Cancer Therapy (FACT-F)After six days of therapy
Number of participants with treatment-related adverse events and severity of these adverse events.After three and six days of treatment

We will check for methylphenidate-related adverse events as: restlessness, hyperactivity, hyporexia, nausea and vomiting, dry mouth, palpitations, sleep insomnia, cephalea, muscle cramps, tics, and any other adverse event that could be treatment-related according to investigator. We will include the severity of the adverse event (mild, moderate, or severe), the presumed relationship with treatment, the measured required to treat it, and the final outcome.

Cognitive level.After three and six days of treatment

We use a specific questionnaire. In order to facilitate its use in fatigued patients it is designed with a limited number of items selected from three validated tools as MMSE, 3MS, and RBANS

Trial Locations

Locations (1)

Clinica Universidad de Navarra

🇪🇸

Pamplona, Navarra, Spain

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