- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT00614575
Survey on PD Patients With Depressive Symptoms
BI_Sifrol Tablets Special Drug Use Surveillance(Survey on the Safety and Efficacy in Parkinson's Disease Patients With Depressive Symptoms)
The primary objective of this investigation is to conduct a 12-week prospective survey in PD patients with depressive symptoms treated with BI Sifrol Tablets (hereinafter referred to as this drug) in the routine clinical settings to determine the following items related to the safety and efficacy.
i. Adverse drug reaction symptoms, incidence, and severity ii. Motor capacity during the investigation iii. Depressive symptoms during the investigation
Přehled studie
Postavení
Podmínky
Typ studie
Zápis (Aktuální)
Kontakty a umístění
Studijní místa
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Akashi, Japonsko
- Boehringer Ingelheim Investigational Site
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Akita, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Akita, Japonsko
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Asahikawa, Japonsko
- Boehringer Ingelheim Investigational Site
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Ashikaga, Japonsko
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Awaji, Japonsko
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Chitose, Japonsko
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Chuo, Japonsko
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Fuchu, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Fuchu, Japonsko
- Boehringer Ingelheim Investigational Site 2
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Fuefuki, Japonsko
- Boehringer Ingelheim Investigational Site
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Fuehuki, Japonsko
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Fujioka, Japonsko
- Boehringer Ingelheim Investigational Site
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Fujisaki, Japonsko
- Boehringer Ingelheim Investigational Site
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Fujisawa, Japonsko
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Fukaya, Japonsko
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Fukuoka, Japonsko
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Fukuoka, Japonsko
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Fukuoka, Japonsko
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Fukuoka, Japonsko
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Fukuoka, Japonsko
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Fukushima, Japonsko
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Fukushima, Japonsko
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Funabashi, Japonsko
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Gifu, Japonsko
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Gifu, Japonsko
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Habikino, Japonsko
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Hachioji, Japonsko
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Hamamatsu, Japonsko
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Hamamatsu, Japonsko
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Hamamatsu, Japonsko
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Hamamatsu, Japonsko
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Hamamatsu, Japonsko
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Hanamaki, Japonsko
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Hayashima, Japonsko
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Higashiosaka, Japonsko
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Higashiosaka, Japonsko
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Himeji, Japonsko
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Hirakata, Japonsko
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Hirishima, Japonsko
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Hirosaki, Japonsko
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Ibaragi, Japonsko
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Iizuka, Japonsko
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Inag, Japonsko
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Irima, Japonsko
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Isahaya, Japonsko
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Iwaki, Japonsko
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Iwamizawa, Japonsko
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Iwata, Japonsko
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Jyoetsu, Japonsko
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Jyoetsu, Japonsko
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Jyoyo, Japonsko
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Kagoshima, Japonsko
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Kagoshima, Japonsko
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Kagoshima, Japonsko
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Kahoku, Japonsko
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Kamakura, Japonsko
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Kanazawa, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Kanazawa, Japonsko
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Kanoya, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Kanoya, Japonsko
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Kashihara, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Kashihara, Japonsko
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Kasuga, Japonsko
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Kawagchi, Japonsko
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Kawaguchi, Japonsko
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Kawasaki, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Kawasaki, Japonsko
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Kitakami, Japonsko
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Kiyose, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Kiyose, Japonsko
- Boehringer Ingelheim Investigational Site 2
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Kodaira, Japonsko
- Boehringer Ingelheim Investigational Site
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Kofu, Japonsko
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Koga, Japonsko
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Komae, Japonsko
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Komatsu, Japonsko
- Boehringer Ingelheim Investigational Site
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Komatsushima, Japonsko
- Boehringer Ingelheim Investigational Site
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Koriyama, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Koriyama, Japonsko
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Koshigaya, Japonsko
- Boehringer Ingelheim Investigational Site
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Kumamoto, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Kumamoto, Japonsko
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Kumamoto, Japonsko
- Boehringer Ingelheim Investigational Site 3
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Kure, Japonsko
- Boehringer Ingelheim Investigational Site
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Kusatsu, Japonsko
- Boehringer Ingelheim Investigational Site
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Kyoto, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Kyoto, Japonsko
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Kyoto, Japonsko
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Kyoto, Japonsko
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Maebashi, Japonsko
- Boehringer Ingelheim Investigational Site
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Matsudo, Japonsko
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Matsumoto, Japonsko
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Mibu, Japonsko
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Mihara, Japonsko
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Mihoro, Japonsko
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Miriyama, Japonsko
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Misato, Japonsko
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Miyako, Japonsko
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Miyazaki, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Miyazaki, Japonsko
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Moriguchi, Japonsko
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Morioka, Japonsko
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Morioka, Japonsko
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Moriya, Japonsko
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Musashino, Japonsko
- Boehringer Ingelheim Investigational Site
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Nagano, Japonsko
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Nagaoka, Japonsko
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Nagaokakyo, Japonsko
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Nagoya, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Nagoya, Japonsko
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Nagoya, Japonsko
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Nagoya, Japonsko
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Nara, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Nara, Japonsko
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Narashino, Japonsko
- Boehringer Ingelheim Investigational Site
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Narita, Japonsko
- Boehringer Ingelheim Investigational Site
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Naruto, Japonsko
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Nasushiobara, Japonsko
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Nichinan, Japonsko
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Ninohe, Japonsko
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Nishinomiya, Japonsko
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Nishitokyo, Japonsko
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Ogaki, Japonsko
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Oiso, Japonsko
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Oita, Japonsko
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Oita, Japonsko
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Oita, Japonsko
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Okaya, Japonsko
- Boehringer Ingelheim Investigational Site
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Okayama, Japonsko
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Okayama, Japonsko
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Okazaki, Japonsko
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Okinawa, Japonsko
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Omura, Japonsko
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Omuta, Japonsko
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Onojyo, Japonsko
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Osaka, Japonsko
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Osaka, Japonsko
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Osaka, Japonsko
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Osaka, Japonsko
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Osaka, Japonsko
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Osaka, Japonsko
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Ota, Japonsko
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Otake, Japonsko
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Otsu, Japonsko
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Ryugasaki, Japonsko
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Saeki, Japonsko
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Saga, Japonsko
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Sagamihara, Japonsko
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Sagamihara, Japonsko
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Sagamihara, Japonsko
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Saijyo, Japonsko
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Saitama, Japonsko
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Sakai, Japonsko
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Sakai, Japonsko
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Sapporo, Japonsko
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Sapporo, Japonsko
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Sapporo, Japonsko
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Sapporo, Japonsko
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Sapporo, Japonsko
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Sapporo, Japonsko
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Sapporo, Japonsko
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Sapporo, Japonsko
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Sapporo, Japonsko
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Sekigahara, Japonsko
- Boehringer Ingelheim Investigational Site
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Sendai, Japonsko
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Sendai, Japonsko
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Shimoda, Japonsko
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Shimotsuke, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Shimotsuke, Japonsko
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Shinngu, Japonsko
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Shiroishi, Japonsko
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Shizuoka, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Shizuoka, Japonsko
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Showajima, Japonsko
- Boehringer Ingelheim Investigational Site
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Suita, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Suita, Japonsko
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Susono, Japonsko
- Boehringer Ingelheim Investigational Site
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Suzuka, Japonsko
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Takaoka, Japonsko
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Takaoka, Japonsko
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Takatsuki, Japonsko
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Tarimizu, Japonsko
- Boehringer Ingelheim Investigational Site
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Togitsu, Japonsko
- Boehringer Ingelheim Investigational Site
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Tokoname, Japonsko
- Boehringer Ingelheim Investigational Site
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Tokushima, Japonsko
- Boehringer Ingelheim Investigational Site
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Tokyo Arakawa-ku, Japonsko
- Boehringer Ingelheim Investigational Site
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Tokyo Bunkyo-ku, Japonsko
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Tokyo Chuo-ku, Japonsko
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Tokyo Chuo-ku, Japonsko
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Tokyo Daito-ku, Japonsko
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Tokyo Koto-ku, Japonsko
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Tokyo Meguro-ku, Japonsko
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Tokyo Meguro-ku, Japonsko
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Tokyo Minato-ku, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Tokyo Minato-ku, Japonsko
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Tokyo Minato-ku, Japonsko
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Tokyo Nakano-ku, Japonsko
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Tokyo Nerima-ku, Japonsko
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Tokyo Ota-ku, Japonsko
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Tokyo Ota-ku, Japonsko
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Tokyo Setagaya, Japonsko
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Tokyo Setagaya-ku, Japonsko
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Tokyo Shibuya-ku, Japonsko
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Tokyo Shinagawa-ku, Japonsko
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Tokyo Shinjyuku-ku, Japonsko
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Tokyo Shinjyuku-ku, Japonsko
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Tokyo Shinjyuku-ku, Japonsko
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Tokyo Sibuya-ku, Japonsko
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Tokyo Toshima-ku, Japonsko
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Tokyo-Edogawa-ku, Japonsko
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Tokyo-Itabashi-ku, Japonsko
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Toride, Japonsko
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Tosu, Japonsko
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Toyama, Japonsko
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Toyama, Japonsko
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Toyama, Japonsko
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Toyohashi, Japonsko
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Toyokawa, Japonsko
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Toyonaka, Japonsko
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Ube, Japonsko
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Uchinada, Japonsko
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Ueda, Japonsko
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Ushiku, Japonsko
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Utsunomiya, Japonsko
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Utsunomiya, Japonsko
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Wakayama, Japonsko
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Yachiyo, Japonsko
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Yachiyo, Japonsko
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Yachiyo, Japonsko
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Yamanashi, Japonsko
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Yanago, Japonsko
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Yoichi, Japonsko
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Yokohama, Japonsko
- Boehringer Ingelheim Investigational Site 1
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Yokohama, Japonsko
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Yokohama, Japonsko
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Yokohama, Japonsko
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Yokosuka, Japonsko
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Yoshinogawa, Japonsko
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Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Metoda odběru vzorků
Studijní populace
Popis
Inclusion criteria:
**PD patients with depressive symptoms Patients who have not received pramipexole hydrochloride hydrate preparations within 1 month before survey entrance.
Exclusion criteria:
- PD patients with the past history of suicidal attempt, suicidal ideation or tendency
- PD patients with suicidal ideation
- PD patients with the past history of suicidal tendency
Studijní plán
Jak je studie koncipována?
Detaily designu
Kohorty a intervence
Skupina / kohorta |
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BI-Sifrol® Tablets (Pramipexole)
BI-Sifrol® Tablets, pramipexole dose: 0.125 mg, 0.5 mg, No reference therapy
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Percentage of Participants With Adverse Events, Adverse Drug Reactions, and Serious Adverse Events
Časové okno: for 12 weeks
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The aim of this Post Marketing Surveillance (PMS) was to obtain safety data with treatment of pramipexole in Parkinson's disease patients with depressive symptoms.
The percentage of participants with adverse events, adverse drug reactions, and serious adverse events are presented.
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for 12 weeks
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Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Clinical Global Impression of Improvement
Časové okno: for 12 weeks after initiation of the treatment
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Investigators evaluation of the Parkinson's disease (PD) symptoms on the Clinical Global Impression (CGI) with 5 categories (very much improved, much improved, minimally improved, no effect, and unassessable).
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for 12 weeks after initiation of the treatment
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Mean Change From Baseline in Unified Parkinson's Disease Rating Scale (UPDRS) Part III Total Score
Časové okno: Baseline and after 12 weeks (or at the time of discontinuation)
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Part III of the UPDRS contains the clinician-scored motor evaluation, and includes 14 individual items each scored from 0 (Normal) to 4 (Extreme dysfunction).
The total score ranged from 0 to 56.
A negative change in the Part III total score indicates improvement.
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Baseline and after 12 weeks (or at the time of discontinuation)
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Mean Change From Baseline in Beck's Depression Inventory (BDI) Total Score
Časové okno: Baseline and after 12 weeks (or at the time of discontinuation)
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The degree of severity in depressive state are scored between 0-63 in BDI.
A decrease in the score means improvement.
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Baseline and after 12 weeks (or at the time of discontinuation)
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Mean Change From Baseline in UPDRS (Unified Parkinson's Disease Rating Scale) Part I Item 3 Score
Časové okno: Baseline and after 12 weeks (or at the time of discontinuation)
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Unified Parkinson's Disease Rating Scale Part I Item 3 assesses the participant for symptoms of depression.
Item 3 scores range from 0 (None) to 4 (Sustained depression with suicidal thoughts or intent).
A higher score indicates more severe depression symptoms.
A negative change in the item 3 score indicates improvement.
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Baseline and after 12 weeks (or at the time of discontinuation)
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Mean Change From Baseline in Modified Hoehn & Yahr Rating Scale
Časové okno: After 12 weeks or at the time of discontinuation
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This scale is an investigator-completed assessment of the degree of complications arising from Parkinson's disease.
The scale ranges from 0 (No signs) to 5 (Bedridden).
A negative change in the Yahr rating scale indicates improvement.
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After 12 weeks or at the time of discontinuation
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Spolupracovníci a vyšetřovatelé
Sponzor
Publikace a užitečné odkazy
Užitečné odkazy
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia
Primární dokončení (Aktuální)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Odhad)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Odhad)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Další relevantní podmínky MeSH
Další identifikační čísla studie
- 248.635
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .
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-
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-
CND Life SciencesDigestive Disease Associates of CTNáborParkinsonova choroba | Parkinson | PARKINSONOVA NEMOC (porucha) | Parkinsonova chorobaSpojené státy
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University of Sao Paulo General HospitalInCor Heart InstituteDokončenoSrdeční arytmie | Cesta pro příslušenství | Wolf Parkinson White syndromBrazílie