Conventional Versus Automated Measurement of Blood Pressure in the Office (The CAMBO Study)

Phase 4

Completed

• Conditions: Hypertension

• Registration Number: NCT00325832
• Lead Sponsor: Sunnybrook Health Sciences Centre

Brief Summary

To determine if the use of automated office blood pressure readings can improve management of systolic hypertension in routine clinical practice. Automated office SBP recordings in routine clinical practice using the BpTRU device will reflect more accurately the mean awake ambulatory systolic BP than will manual BP readings taken with conventional mercury sphygmomanometry. This should lead to improvements in the management of systolic hypertension with optimization of drug therapy in practices using the BpTRU device.

Detailed Description

Not available

Study Timeline

• Study Start: 2006-01
• Study First Submitted: 2006-05-12
• Study First Submitted QC: 2006-05-12
• Study First Posted: 2006-05-15
• Status Verified: 2008-05
• Last Update Submitted: 2010-08-20
• Last Update Posted: 2010-08-23

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 750

Inclusion Criteria

• Both treated and untreated patients with systolic hypertension under routine FP care
• For untreated patients, routine office SBP as measured by the patient's FP at the last routine office visit using a mercury device must have SBP ≥ 160 mmHg and DBP <= 95 mmHg
• For patients already receiving antihypertensive therapy, the last routine office BP as measured by the patient's FP using mercury sphygmomanometry must be SBP ≥ 140 mmHg and DBP <= 90 mmHg

Exclusion Criteria

• Presence of target organ damage such as MI, stroke, and serum creatinine twice normal
• Diabetes mellitus treated with insulin or oral hypoglycemic therapy
• Secondary hypertension
• Participation in another research study involving measurement of BP
• Patient's insistence on using self BP measurement outside of the study
• Any conditions or circumstances which might preclude the successful completion of the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: FACTORIAL

Primary Outcome Measures

Name	Time	Method
ambulatory blood pressure

Trial Locations

Locations (1)

Sunnybrook Health Sciences Centre; 🇨🇦 Toronto, Ontario, Canada