TY - JOUR
T1 - The Combination Therapy of Hypertension to Prevent Cardiovascular Events (COPE) trial
T2 - Rationale and design
AU - Ogihara, Toshio
AU - Matsuzaki, Masunori
AU - Matsuoka, Hiroaki
AU - Shimamoto, Kazuaki
AU - Shimada, Kazuyuki
AU - Rakugi, Hiromi
AU - Umemoto, Seiji
AU - Kamiya, Akira
AU - Suzuki, Norihiro
AU - Kumagai, Hiroo
AU - Ohashi, Yasuo
AU - Takishita, Shuichi
AU - Abe, Keishi
AU - Saruta, Takao
AU - Kikuchi, K.
AU - Itoh, S.
AU - Suzuki, H.
AU - Fujita, T.
AU - Higaki, J.
AU - Etoh, T.
AU - Tei, C.
AU - Nogawa, S.
AU - Yoshikawa, T.
AU - Yumura, K.
AU - Utsunomiya, K.
AU - Kario, K.
AU - Kitagawa, K.
AU - Makino, H.
AU - Matsumoto, M.
AU - Hayashi, K.
AU - Kawana, M.
AU - Fujishima, M.
AU - Otsuka, K.
AU - Tanabe, K.
PY - 2005/4
Y1 - 2005/4
N2 - A number of major clinical trials have demonstrated the clinical benefits of lowering blood pressure and have indicated that a majority of patients with hypertension will require more than one drug to achieve optimal blood pressure control. However, there is little data showing which antihypertensive combination best protects patients from cardiovascular events and which best achieves the target blood pressure with the fewest adverse events. The Combination Therapy of Hypertension to Prevent Cardiovascular Events (COPE) trial is the first large-scale investigator-initiated multicenter study with a prospective, randomized, open, blinded endpoint evaluation (PROBE) design to directly compare cardiovascular mortality and morbidity, incidence of adverse drug reaction, and degree of blood pressure reduction in Japanese hypertensive patients for a combination of angiotensin receptor blockers, β-blockers or thiazide diuretics in addition to a calcium antagonist, benidipine hydrochloride, with a response-dependent dose titration scheme. The COPE trial is being conducted with the cooperation of more than 100 centers and clinics in Japan and involves 3,000 patients, who will be followed for 3 years. Eligible patients are being enrolled from May 2003 until May 2006. Results from the COPE trial should provide new evidence for selecting optimal combination therapies for hypertensive patients.
AB - A number of major clinical trials have demonstrated the clinical benefits of lowering blood pressure and have indicated that a majority of patients with hypertension will require more than one drug to achieve optimal blood pressure control. However, there is little data showing which antihypertensive combination best protects patients from cardiovascular events and which best achieves the target blood pressure with the fewest adverse events. The Combination Therapy of Hypertension to Prevent Cardiovascular Events (COPE) trial is the first large-scale investigator-initiated multicenter study with a prospective, randomized, open, blinded endpoint evaluation (PROBE) design to directly compare cardiovascular mortality and morbidity, incidence of adverse drug reaction, and degree of blood pressure reduction in Japanese hypertensive patients for a combination of angiotensin receptor blockers, β-blockers or thiazide diuretics in addition to a calcium antagonist, benidipine hydrochloride, with a response-dependent dose titration scheme. The COPE trial is being conducted with the cooperation of more than 100 centers and clinics in Japan and involves 3,000 patients, who will be followed for 3 years. Eligible patients are being enrolled from May 2003 until May 2006. Results from the COPE trial should provide new evidence for selecting optimal combination therapies for hypertensive patients.
KW - Benidipine
KW - Combination therapy
KW - Hypertension
KW - Multicenter clinical trial
KW - PROBE (prospestive, randomized, open, blinded endpoint evaluation)
UR - http://www.scopus.com/inward/record.url?scp=21244464728&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=21244464728&partnerID=8YFLogxK
U2 - 10.1291/hypres.28.331
DO - 10.1291/hypres.28.331
M3 - Article
C2 - 16138563
AN - SCOPUS:21244464728
SN - 0916-9636
VL - 28
SP - 331
EP - 338
JO - Hypertension Research
JF - Hypertension Research
IS - 4
ER -