Viewing Study NCT00926289



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Last Modification Date: 2024-10-26 @ 10:07 AM
Study NCT ID: NCT00926289
Status: COMPLETED
Last Update Posted: 2014-06-27
First Post: 2009-06-22

Brief Title: Telmisartan 80mg Plus Hydrochlorothiazide 25mg First Line in Moderate or Severe Hypertension
Sponsor: Boehringer Ingelheim
Organization: Boehringer Ingelheim

Study Overview

Official Title: A Randomised Double-blind Double Dummy Active Controlled Parallel Group Forced Titration Study to Compare the Fixed-dose Combination of Telmisartan 80mg Plus Hydrochlorothiazide 25mg T80HCTZ25 Versus Telmisartan 80mg T80 Monotherapy as First Line Therapy in Patients With Grade 2 or Grade 3 Hypertension Systolic Blood Pressure SBP 160 mmHg and Diastolic Blood Pressure DBP 100 mmHg
Status: COMPLETED
Status Verified Date: 2013-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The primary objective of this trial is to demonstrate that the fixed-dose combination of T80HCTZ25 is superior as first line therapy in reducing seated trough cuff Systolic Blood PressureSBP compared to the monotherapy of T80 in patients with grade 2 or grade 3 hypertension SBP160 mmHg and Diastolic Blood PressureDBP100 mmHg
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
2008-007711-32 EUDRACT_NUMBER EudraCT None