search
Back to results

STITCH2 (Simplified Therapeutic Intervention to Control Hypertension and Hypercholesterolemia) (STITCH2)

Primary Purpose

Hypertension, Hypercholesterolemia

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Treatment algorithm:caduet, Amlodipine, ACEI-ARB combo dose, a-blocker, b-blocker or spironolactone, dyslipidemic therapy with ezetamide
Sponsored by
University of Western Ontario, Canada
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypertension focused on measuring hypertension, hypercholesterolemia, family physicians, fixed dose combination therapy, cluster randomized controlled trial

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • male or female subjects 18 years or older
  • documented diagnoses of hypertension and of hypercholesterolemia or current therapy for these conditions
  • uncontrolled hypertension (SBP >140 mmHg or DBP >90 mmHg) or cholesterol levels above their threshold based on their global atherosclerotic risk profile (based on ATP III assessment)
  • ability to give written informed consent

Exclusion Criteria:

  • ischemic heart disease, atrial fibrillation, chronic kidney disease and significant liver disease
  • currently prescribed 3 or more drugs to control blood pressure
  • currently prescribed 2 or more drugs to control hypercholesterolemia
  • participating in other hypertension/hypercholesterolemia studies

Sites / Locations

  • Robarts Research Insititute

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

1

2

Arm Description

Drug: Fix dose combination therapy

Guidelines based management

Outcomes

Primary Outcome Measures

Proportion of subjects whose systolic BP [SBP] <140 mmHg and diastolic BP [DBP] <90 mmHg)or proportion whose cholesterol levels are at or below threshold based on their global artherosclerotic risk profile compared at the practice level.

Secondary Outcome Measures

Secondary measures include the change at 6 months in SBP and DBP and cholesterol levels. These outcomes will be compared at the practice level

Full Information

First Posted
March 3, 2008
Last Updated
June 13, 2012
Sponsor
University of Western Ontario, Canada
Collaborators
Pfizer
search

1. Study Identification

Unique Protocol Identification Number
NCT00637078
Brief Title
STITCH2 (Simplified Therapeutic Intervention to Control Hypertension and Hypercholesterolemia)
Acronym
STITCH2
Official Title
Evaluation of a Primary Treatment Algorithm Using Combination Therapy for the Management of Patients With Hypertension and Hypercholesterolemia
Study Type
Interventional

2. Study Status

Record Verification Date
June 2012
Overall Recruitment Status
Completed
Study Start Date
February 2008 (undefined)
Primary Completion Date
June 2010 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Western Ontario, Canada
Collaborators
Pfizer

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of this study is to assess if the implementation of a treatment algorithm including initial treatment with a low dose diuretic/ACE-inhibitor or ARB combination and subsequently a low dose DHP-CCB/statin combination will improve the management of hypertension/hypercholesterolemia compared to guidelines-base management at family practices.
Detailed Description
Utilization of fixed dose combination therapy has been advocated as an adherence-enhancing strategy and has been so recommended in the 2007 Canadian Hypertension Education Program (CHEP) recommendations. Further, in a previous study (STITCH) it was demonstrated that a simplified treatment algorithm utilizing initial therapy with a low dose fixed-dose combination therapy improved blood pressure control in hypertensive patients. However, the effectiveness of either a simplified treatment algorithm or the initial use of fixed dose combination therapies for 2 risk factors in hypertensive dyslipidemic patients has yet to be determined. Therefore, the current study is designed to determine whether utilization of a fixed dose combination hypertension/hypercholesterolemia therapy results in improved adherence, patient satisfaction as well as improved rates of reaching target LDL cholesterol and blood pressure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Hypercholesterolemia
Keywords
hypertension, hypercholesterolemia, family physicians, fixed dose combination therapy, cluster randomized controlled trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1000 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Drug: Fix dose combination therapy
Arm Title
2
Arm Type
No Intervention
Arm Description
Guidelines based management
Intervention Type
Other
Intervention Name(s)
Treatment algorithm:caduet, Amlodipine, ACEI-ARB combo dose, a-blocker, b-blocker or spironolactone, dyslipidemic therapy with ezetamide
Intervention Description
initial treatment with a low dose diuretic/ACE-inhibitor or ARB combination followed by a low dose DHP-CCB/statin combination
Primary Outcome Measure Information:
Title
Proportion of subjects whose systolic BP [SBP] <140 mmHg and diastolic BP [DBP] <90 mmHg)or proportion whose cholesterol levels are at or below threshold based on their global artherosclerotic risk profile compared at the practice level.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Secondary measures include the change at 6 months in SBP and DBP and cholesterol levels. These outcomes will be compared at the practice level
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: male or female subjects 18 years or older documented diagnoses of hypertension and of hypercholesterolemia or current therapy for these conditions uncontrolled hypertension (SBP >140 mmHg or DBP >90 mmHg) or cholesterol levels above their threshold based on their global atherosclerotic risk profile (based on ATP III assessment) ability to give written informed consent Exclusion Criteria: ischemic heart disease, atrial fibrillation, chronic kidney disease and significant liver disease currently prescribed 3 or more drugs to control blood pressure currently prescribed 2 or more drugs to control hypercholesterolemia participating in other hypertension/hypercholesterolemia studies
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ross Feldman, MD
Organizational Affiliation
Deputy Director
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
George Dresser, MD
Organizational Affiliation
Co prinicipal investigator
Official's Role
Principal Investigator
Facility Information:
Facility Name
Robarts Research Insititute
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5K8
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

STITCH2 (Simplified Therapeutic Intervention to Control Hypertension and Hypercholesterolemia)

We'll reach out to this number within 24 hrs