Evaluation of the Additional Efficacy, and Safety of Olmesartan Medoxomil 20mg / Hydrochlorothiazide 12.5mg in the Treatment of Chinese Patients With Mild to Moderate Essential Hypertension

PHASE3CompletedINTERVENTIONAL
Enrollment

304

Participants

Timeline

Start Date

August 31, 2006

Primary Completion Date

July 31, 2007

Study Completion Date

August 31, 2007

Conditions
Essential Hypertension
Interventions
DRUG

olmesartan medoxomil + hydrochlorothiazide

olmesartan medoxomil 20mg oral tablets, once daily for 4 weeks then olmesartan medoxomil 20mg oral tablets + hydrochlorothiazide 12.5 mg oral tablets, once daily for up to 8 weeks

DRUG

olmesartan medoxomil

olmesartan medoxomil 20mg oral tablets, once daily for 4 weeks then olmesartan medoxomil 40mg oral tablets, once daily for up to 8 weeks

Trial Locations (8)

Unknown

Beijing

Chengdu

Chongqing

Guangzhou

Hangzhou

Nanjing

Shanghai

Wuhan

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Shanghai Sankyo Pharmaceuticals Co., Ltd.

UNKNOWN

lead

Daiichi Sankyo

INDUSTRY

NCT00872586 - Evaluation of the Additional Efficacy, and Safety of Olmesartan Medoxomil 20mg / Hydrochlorothiazide 12.5mg in the Treatment of Chinese Patients With Mild to Moderate Essential Hypertension | Biotech Hunter | Biotech Hunter