Last updated: 11/07/2018 01:11:10
A randomized, double-blind, parallel group, multicenter study comparing antihypertensive effects of escalating doses of carvedilol MR to placebo in patients with mild to moderate hypertension
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A randomized, double-blind, parallel group, multicenter study comparing antihypertensive effects of escalating doses of carvedilol MR to placebo in patients with mild to moderate hypertension
Trial description: A randomized, double-blind, parallel group, multicenter study comparing antihypertensive effects of escalating doses of carvedilol MR to placebo in patients with mild to moderate hypertension
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Weber MA, Bakris GL, Tarka EA, Iyengar M, Fleck R, Sica DA. Efficacy of a once-daily formulation of carvedilol for the treatment of hypertension. Journal of Clinical Hypertension 2006, 8(12) 840-849.
Weber MA, Sica DA, Tarka EA, Iyengar M, Fleck R, Bakris GL. Controlled-release carvedilol in the treatment of essential hypertension. American Journal of Cardiology 2006, 98(7A Suppl S):32L-38L..
Medical condition
Hypertension
Product
carvedilol
Collaborators
Not applicable
Study date(s)
September 2004 to June 2005
Type
Not applicable
Phase
3
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Clinical study report
Available language(s): English
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
Not applicable
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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