- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00613756
Special Survey on PD Patients With Renal Dysfunction
12. november 2013 opdateret af: Boehringer Ingelheim
Post Marketing Surveillance of BI-Sifrol® (Pramipexole). Special Survey on Patients With Parkinson's Disease and Renal Dysfunction
The survey is conducted to collect safety and effectiveness information targeting patients who have both Parkinson's disease and renal dysfunction treated with Pramipexole in the daily clinical settings in Japan.
Studieoversigt
Status
Afsluttet
Betingelser
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
107
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Asahikawa, Japan
- Boehringer Ingelheim Investigational Site
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Azumino, Japan
- Boehringer Ingelheim Investigational Site
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Chuo, Japan
- Boehringer Ingelheim Investigational Site
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Eiheiji, Japan
- Boehringer Ingelheim Investigational Site
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Fuji, Japan
- Boehringer Ingelheim Investigational Site
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Fujinomiya, Japan
- Boehringer Ingelheim Investigational Site
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Fujisaki, Japan
- Boehringer Ingelheim Investigational Site
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Fukaya, Japan
- Boehringer Ingelheim Investigational Site
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Fukui, Japan
- Boehringer Ingelheim Investigational Site
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Fukuoka, Japan
- Boehringer Ingelheim Investigational Site
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Gifu, Japan
- Boehringer Ingelheim Investigational Site
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Hachioji, Japan
- Boehringer Ingelheim Investigational Site
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Hamamatsu, Japan
- Boehringer Ingelheim Investigational Site
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Himeji, Japan
- Boehringer Ingelheim Investigational Site
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Hiroshima, Japan
- Boehringer Ingelheim Investigational Site
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Ichinoseki, Japan
- Boehringer Ingelheim Investigational Site
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Iga, Japan
- Boehringer Ingelheim Investigational Site
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Iida, Japan
- Boehringer Ingelheim Investigational Site
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Ina, Japan
- Boehringer Ingelheim Investigational Site
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Inazawa, Japan
- Boehringer Ingelheim Investigational Site
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Isehara, Japan
- Boehringer Ingelheim Investigational Site
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Isezaki, Japan
- Boehringer Ingelheim Investigational Site
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Iwamizawa, Japan
- Boehringer Ingelheim Investigational Site
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Kagoshima, Japan
- Boehringer Ingelheim Investigational Site
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Kajiki, Japan
- Boehringer Ingelheim Investigational Site
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Kanoya, Japan
- Boehringer Ingelheim Investigational Site
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Kashiwazaki, Japan
- Boehringer Ingelheim Investigational Site
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Kawagoe, Japan
- Boehringer Ingelheim Investigational Site
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Kawasaki, Japan
- Boehringer Ingelheim Investigational Site
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Koga, Japan
- Boehringer Ingelheim Investigational Site
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Komae, Japan
- Boehringer Ingelheim Investigational Site
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Koriyama, Japan
- Boehringer Ingelheim Investigational Site
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Koshigaya, Japan
- Boehringer Ingelheim Investigational Site
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Kurashiki, Japan
- Boehringer Ingelheim Investigational Site
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Kyoto, Japan
- Boehringer Ingelheim Investigational Site
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Maebashi, Japan
- Boehringer Ingelheim Investigational Site
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Marugame, Japan
- Boehringer Ingelheim Investigational Site
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Matsudo, Japan
- Boehringer Ingelheim Investigational Site
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Matsumoto, Japan
- Boehringer Ingelheim Investigational Site
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Miki, Japan
- Boehringer Ingelheim Investigational Site
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Mito, Japan
- Boehringer Ingelheim Investigational Site
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Miyazaki, Japan
- Boehringer Ingelheim Investigational Site
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Miyoshi, Japan
- Boehringer Ingelheim Investigational Site
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Mooka, Japan
- Boehringer Ingelheim Investigational Site
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Morioka, Japan
- Boehringer Ingelheim Investigational Site
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Moroyama, Japan
- Boehringer Ingelheim Investigational Site
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Nagahama, Japan
- Boehringer Ingelheim Investigational Site
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Nagakute, Japan
- Boehringer Ingelheim Investigational Site
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Nagasaki, Japan
- Boehringer Ingelheim Investigational Site
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Nagoya, Japan
- Boehringer Ingelheim Investigational Site
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Nanao, Japan
- Boehringer Ingelheim Investigational Site
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Nangoku, Japan
- Boehringer Ingelheim Investigational Site
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Narita, Japan
- Boehringer Ingelheim Investigational Site
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Nishinomiya, Japan
- Boehringer Ingelheim Investigational Site
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Ogaki, Japan
- Boehringer Ingelheim Investigational Site
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Oita, Japan
- Boehringer Ingelheim Investigational Site
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Okawa, Japan
- Boehringer Ingelheim Investigational Site
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Okayama, Japan
- Boehringer Ingelheim Investigational Site
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Okinawa, Japan
- Boehringer Ingelheim Investigational Site
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Onga, Japan
- Boehringer Ingelheim Investigational Site
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Onojo, Japan
- Boehringer Ingelheim Investigational Site
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Osaka, Japan
- Boehringer Ingelheim Investigational Site
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Oshu, Japan
- Boehringer Ingelheim Investigational Site
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Sado, Japan
- Boehringer Ingelheim Investigational Site
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Sagamihara, Japan
- Boehringer Ingelheim Investigational Site
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Saitama, Japan
- Boehringer Ingelheim Investigational Site
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Sanjo, Japan
- Boehringer Ingelheim Investigational Site
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Sapporo, Japan
- Boehringer Ingelheim Investigational Site
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Sekigahara, Japan
- Boehringer Ingelheim Investigational Site
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Shimotsuke, Japan
- Boehringer Ingelheim Investigational Site
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Shingu, Japan
- Boehringer Ingelheim Investigational Site
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Shunan, Japan
- Boehringer Ingelheim Investigational Site
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Suita, Japan
- Boehringer Ingelheim Investigational Site
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Takasago, Japan
- Boehringer Ingelheim Investigational Site
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Takatsuki, Japan
- Boehringer Ingelheim Investigational Site
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Togitsu, Japan
- Boehringer Ingelheim Investigational Site
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Tokyo Adachi-ku, Japan
- Boehringer Ingelheim Investigational Site
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Tokyo Bunkyo-ku, Japan
- Boehringer Ingelheim Investigational Site
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Tokyo Chiyoda-ku, Japan
- Boehringer Ingelheim Investigational Site
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Tokyo Itabashi-ku, Japan
- Boehringer Ingelheim Investigational Site
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Tokyo Meguro-ku, Japan
- Boehringer Ingelheim Investigational Site
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Tokyo Ota-ku, Japan
- Boehringer Ingelheim Investigational Site
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Tokyo Setagaya-ku, Japan
- Boehringer Ingelheim Investigational Site
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Tokyo Shibuya-ku, Japan
- Boehringer Ingelheim Investigational Site
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Tokyo Shinjuku-ku, Japan
- Boehringer Ingelheim Investigational Site
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Tokyo Suginami-ku, Japan
- Boehringer Ingelheim Investigational Site
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Toride, Japan
- Boehringer Ingelheim Investigational Site
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Toyoake, Japan
- Boehringer Ingelheim Investigational Site
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Tsukuba, Japan
- Boehringer Ingelheim Investigational Site
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Uki, Japan
- Boehringer Ingelheim Investigational Site
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Wakayama, Japan
- Boehringer Ingelheim Investigational Site
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Yamagata, Japan
- Boehringer Ingelheim Investigational Site
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Yamaguchi, Japan
- Boehringer Ingelheim Investigational Site
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Yokohama, Japan
- Boehringer Ingelheim Investigational Site
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Yokosuka, Japan
- Boehringer Ingelheim Investigational Site
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Yonago, Japan
- Boehringer Ingelheim Investigational Site
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Yoshinogawa, Japan
- Boehringer Ingelheim Investigational Site
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Yufu, Japan
- Boehringer Ingelheim Investigational Site
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
20 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Patients with idiopathic PD with renal dysfunction from Primary Care setting.
Beskrivelse
Inclusion Criteria:
Patients with Parkinson's disease who have renal dysfunction with pretreatment creatinine clearance =<70mL/min or whose renal dysfunction was determined by the physician
Exclusion Criteria:
None
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Incidence of adverse events
Tidsramme: up to 12 weeks
|
up to 12 weeks
|
|
Incidence of adverse drug reactions (ADRs
Tidsramme: up to 12 weeks
|
up to 12 weeks
|
|
Incidence of serious adverse events (SAEs)
Tidsramme: up to 12 weeks
|
up to 12 weeks
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Modified Hoehn & Yahr rating scale
Tidsramme: change from baseline to week 12
|
change from baseline to week 12
|
|
Unified Parkinson's Disease Rating Scale (UPDRS) part III total score
Tidsramme: change from baseline to week 12
|
change from baseline to week 12
|
|
Physician's overall judgement by medical interview into 4 grades (5 categories)
Tidsramme: week 12
|
week 12
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. februar 2004
Primær færdiggørelse (Faktiske)
1. september 2008
Datoer for studieregistrering
Først indsendt
31. januar 2008
Først indsendt, der opfyldte QC-kriterier
12. februar 2008
Først opslået (Skøn)
13. februar 2008
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
13. november 2013
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
12. november 2013
Sidst verificeret
1. november 2013
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 248.548
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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