Protocol for the Specified Clinical Experience Investigation on the Single Use of Casodex® Tablet 80 mg (CAMON)
Study Overview
Status
Status
Conditions
Conditions
Study Type
Study Type
Enrollment (Actual)
Enrollment
Contacts and Locations
Study Locations
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Aichi, Japan
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Akita, Japan
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Fukuoka, Japan
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Fukushima, Japan
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Gifu, Japan
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Hiroshima, Japan
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Kochi, Japan
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Kumamoto, Japan
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Kyoto, Japan
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Nagasaki, Japan
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Nara, Japan
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Okayama, Japan
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Osaka, Japan
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Saitama, Japan
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Shizuoka, Japan
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Tokushima, Japan
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Tottori, Japan
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Toyama, Japan
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Wakayama, Japan
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Yamagata, Japan
- Research Site
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Aichi
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Houmei, Aichi, Japan
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Inuyama, Aichi, Japan
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Kasugai, Aichi, Japan
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Nagoya, Aichi, Japan
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Okazaki, Aichi, Japan
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Toyohashi, Aichi, Japan
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Toyota, Aichi, Japan
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Akita
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Odate, Akita, Japan
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Aomori
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Hirosaki, Aomori, Japan
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Chiba
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Asahi, Chiba, Japan
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Funahashi, Chiba, Japan
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Ichihara, Chiba, Japan
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Ichikawa, Chiba, Japan
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Narashino, Chiba, Japan
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Sakura, Chiba, Japan
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Ehime
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Imabari, Ehime, Japan
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Matsuyama, Ehime, Japan
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Niihama, Ehime, Japan
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Uwajima, Ehime, Japan
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Fukuoka
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Chikushino, Fukuoka, Japan
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Iizuka, Fukuoka, Japan
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Kasuga, Fukuoka, Japan
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Kita Kyushu, Fukuoka, Japan
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Kurume, Fukuoka, Japan
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Yukuhashi, Fukuoka, Japan
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Fukushima
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Aizuwakamatsu, Fukushima, Japan
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Gifu
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Ibi, Gifu, Japan
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Kani, Gifu, Japan
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Minokamo, Gifu, Japan
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Mizunami, Gifu, Japan
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Ogaki, Gifu, Japan
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Seki, Gifu, Japan
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Yamagata, Gifu, Japan
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Yourou, Gifu, Japan
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Gunma
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Isesaki, Gunma, Japan
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Kiryu, Gunma, Japan
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Numata, Gunma, Japan
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Ohta, Gunma, Japan
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Takasaki, Gunma, Japan
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Hokkaido
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Asahikawa, Hokkaido, Japan
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Eniwa, Hokkaido, Japan
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Kushiro, Hokkaido, Japan
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Sapporo, Hokkaido, Japan
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Sunagawa, Hokkaido, Japan
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Tomakomai, Hokkaido, Japan
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Hyogo
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Akashi, Hyogo, Japan
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Katou, Hyogo, Japan
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Kobe, Hyogo, Japan
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Takarazuka, Hyogo, Japan
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Ibaraki
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Hitachi, Ibaraki, Japan
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Mito, Ibaraki, Japan
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Sashima, Ibaraki, Japan
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Toride, Ibaraki, Japan
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Tsuchiura, Ibaraki, Japan
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Ishihawa
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Hakusan, Ishihawa, Japan
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Iwate
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Ichinoseki, Iwate, Japan
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Kamaishi, Iwate, Japan
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Miyako, Iwate, Japan
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Morioka, Iwate, Japan
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Shiwa, Iwate, Japan
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Kagawa
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Takamatsu, Kagawa, Japan
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Zentrsuji, Kagawa, Japan
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Kagoshima
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Minami Satsuma, Kagoshima, Japan
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Kanagawa
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Atsugi, Kanagawa, Japan
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Chigasaki, Kanagawa, Japan
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Ebina, Kanagawa, Japan
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Kawasaki, Kanagawa, Japan
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Sagamihara, Kanagawa, Japan
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Yamato, Kanagawa, Japan
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Yokohama, Kanagawa, Japan
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Yokosuka, Kanagawa, Japan
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Kyoto
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Nantan, Kyoto, Japan
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Mie
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Inabe, Mie, Japan
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Tsu, Mie, Japan
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Miyagi
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Matsushima, Miyagi, Japan
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Natori, Miyagi, Japan
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Sendai, Miyagi, Japan
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Shiogama, Miyagi, Japan
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Tagajo, Miyagi, Japan
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Nagasaki
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Isahaya, Nagasaki, Japan
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Sasebo, Nagasaki, Japan
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Nara
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Ikoma, Nara, Japan
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Kashiba, Nara, Japan
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Niigata
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Gosen, Niigata, Japan
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Tsubame, Niigata, Japan
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Oita
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Nakatsu, Oita, Japan
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Okayama
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Kurashiki, Okayama, Japan
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Osaka
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Habikino, Osaka, Japan
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Ibaraki, Osaka, Japan
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Ikeda, Osaka, Japan
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Izumisano, Osaka, Japan
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Kaizuka, Osaka, Japan
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Kishiwada, Osaka, Japan
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Matsubara, Osaka, Japan
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Minoo, Osaka, Japan
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Motiguchi, Osaka, Japan
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Neyagawa, Osaka, Japan
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Osaka Sayama, Osaka, Japan
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Sakai, Osaka, Japan
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Suita, Osaka, Japan
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Toyonaka, Osaka, Japan
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Yao, Osaka, Japan
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Saitama
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Asagiri, Saitama, Japan
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Hidaka, Saitama, Japan
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Kawagoe, Saitama, Japan
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Koshigaya, Saitama, Japan
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Kumagaya, Saitama, Japan
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Sayama, Saitama, Japan
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Shimane
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Hamada, Shimane, Japan
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Shizuoka
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Fuji, Shizuoka, Japan
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Fujieda, Shizuoka, Japan
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Hamamatsu, Shizuoka, Japan
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Izu, Shizuoka, Japan
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Shimizu, Shizuoka, Japan
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Tochigi
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Ashikaga, Tochigi, Japan
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Tokushima
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Yoshinogawa, Tokushima, Japan
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Tokyo
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Adachi, Tokyo, Japan
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Arakawa, Tokyo, Japan
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Chiyoda, Tokyo, Japan
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Edogawa, Tokyo, Japan
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Itabashi, Tokyo, Japan
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Katsushika, Tokyo, Japan
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Koutou, Tokyo, Japan
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Minato, Tokyo, Japan
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Musashino, Tokyo, Japan
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Nakano, Tokyo, Japan
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Nishi Tokyo, Tokyo, Japan
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Oota, Tokyo, Japan
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Ota, Tokyo, Japan
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Setagaya, Tokyo, Japan
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Shibuya, Tokyo, Japan
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Shinagawa, Tokyo, Japan
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Shinjyuku, Tokyo, Japan
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Sumida, Tokyo, Japan
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Tachikawa, Tokyo, Japan
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Toshima, Tokyo, Japan
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Toyama
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Kurobe, Toyama, Japan
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Takaoka, Toyama, Japan
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Yamagata
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Kahoku, Yamagata, Japan
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Yamanashi
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Kai, Yamanashi, Japan
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Nirasaki, Yamanashi, Japan
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Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Prostate cancer patients who have no history of receiving endocrine therapy (including surgical castration), and who plan to undergo Casodex® tablets monotherapy for not less than 12 months
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Adverse event incidence
Time Frame: Time since starting Casodex monotherapy, monthly
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Time since starting Casodex monotherapy, monthly
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Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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improvement of prostate cancer using Tumor marker PSA
Time Frame: Time since starting Casodex monotherapy, monthly
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Time since starting Casodex monotherapy, monthly
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Maintenance of sexual function
Time Frame: At 3 months since starting Casodex monotherapy,
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At 3 months since starting Casodex monotherapy,
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Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- NIS-OJP-CAS-2009/1
- CAS002
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.