- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00220506
Fatigue Treatment Using Provigil
Fatigue Treatment Using Provigil in Patients With Relapsing Remitting Multiple Sclerosis
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Multiple sclerosis and fatigue Fatigue is one of the most common symptoms of multiple sclerosis (MS), occurring in 30%-80% of patients and for many of them fatigue is the most disabling symptom (1).
Definition of fatigue according to the MS Council for Clinical Practice Guidelines is as follows: "A subjective lack of physical and/or mental energy that is perceived by the individual or caregiver to interfere with usual and desired activities".
As fatigue is a subjective and non-specific symptom, and can easily be confused with either weakness or depressed mood, both common in MS, the following characteristics have been defined to better diagnose MS-associated fatigue:
- MS-related fatigue generally occurs on a daily basis.
- It tends to worsen as the day progresses.
- It tends to be aggravated by heat and humidity.
- It is not directly correlated with either depression or the degree of physical impairment.
- It may occur first thing in the morning even if the patient has had a restful full night's sleep.
The current medications used for the treatment of MS-associated fatigue such as amantadine hydrochloride and pemoline are useful to some, but not all patients. In a multicenter trial (2) it was found that 100 mg amantadine twice daily significantly improves fatigue. Pemoline in a placebo-controlled trial (3) failed to show significant effect on fatigue in MS patients and was poorly tolerated as side effects occurred in 25% of patients. A third trial (4) compared pemoline to amantadine and placebo, and showed only a positive trend for pemoline, while amantadine had a benefit over placebo in some fatigue measures. There was also a marked placebo effect in this trial, with approximately half of patients reporting improvement in fatigue no matter what treatment (pemoline, amantadine or placebo) they were taking.
In the current study proposal we intend to evaluate the effect of Provigil on MS-associated fatigue.
The possibility for add-on drug that will affect fatigue in MS is of importance, as fatigue has a significant impact on activities of daily living, interfering with work, family life and social activities.
1.2. The fatigue scale named "Fatigue Impact Scale" The awareness of the impact of fatigue on patient's quality of life (QOL) and the need to evaluate the effect of the different therapies on this parameter resulted in the development and validation of different questionnaires for the measurement of fatigue, i.e., the Fatigue Impact Scale (FIS), which has been shown to measure both, fatigue and treatment effect on fatigue (6-9).
The FIS is a reliable and validated 40-items questionnaire that is capable of selecting a treatment effect. It is a made up of 3 sub-scales: physical, cognitive and social. Each question is scored from 0-4, allowing a total score of 160. High scores indicate high impairment.
Undersøgelsestype
Tilmelding
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Tel Hashomer, Israel
- Rekruttering
- Multiple Sclerosis Center
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Kontakt:
- Mark Dolev, MD
- Telefonnummer: 973-3-5303899
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Ledende efterforsker:
- Mark Dolev, MD
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- The patients should be diagnosed with clinically definite MS (Posner criteria).
- EDSS at screening: 0 to 5.5, inclusive.
- Positive Fatigue impact scale 40 points or more.
- Age 18-55 years.
- Co-operating patient, capable of complying with all of trial procedures (i.e. FIS, QOL, etc…).
- Patient who signed written informed consent.
- Women of childbearing potential must use effective birth control method during study.
Exclusion Criteria:
- Life threatening and/or unstable clinical condition which in the opinion of the investigator might compromise trial completion
- A relapse during the last 30 days prior to the study.
- Systemic steroid therapy within 30 days
- Known hypersensitivity or intolerance, to Provigil or related substances or to any component of the formulation.
- Sleep apnea
- Narcolepsy
- Participation in experimental drug trials during the last 30 days prior to the trial.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Crossover opgave
- Maskning: Ingen (Åben etiket)
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
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To determine fatigue impact scale
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Sekundære resultatmål
Resultatmål |
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to determine cognition measurements
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Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Mark Dolev, MD, Sheba medical center
Datoer for undersøgelser
Studer store datoer
Studiestart
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Patologiske processer
- Sygdomme i nervesystemet
- Sygdomme i immunsystemet
- Demyeliniserende autoimmune sygdomme, CNS
- Autoimmune sygdomme i nervesystemet
- Demyeliniserende sygdomme
- Autoimmune sygdomme
- Multipel sclerose
- Sclerose
- Træthed
- Lægemidlers fysiologiske virkninger
- Molekylære mekanismer for farmakologisk virkning
- Cytokrom P-450 enzyminducere
- Cytokrom P-450 CYP3A inducere
- Centralnervesystemets stimulanser
- Vågenhedsfremmende midler
- Modafinil
Andre undersøgelses-id-numre
- SHEBA-05-3769-MD-CTIL
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