Feasibility study of the use of point-of-care NP measurement
Not Applicable
Completed
- Conditions
- Specialty: Primary care, Primary sub-specialty: Cardiovascular diseaseUKCRC code/ Disease: Cardiovascular/ Other forms of heart diseaseCirculatory SystemCardiovascular disease
- Registration Number
- ISRCTN12866009
- Lead Sponsor
- niversity of Oxford
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 27
Inclusion Criteria
1. Participant is willing and able to give informed consent for participation in the study
2. Male or female, aged 18 years or above
3. Confirmed diagnosis of heart failure made by cardiologist and/or echocardiography
4. Currently managed in a primary care setting where the clinician is willing to take part in routine POC NP monitoring
Exclusion Criteria
Participant is considered to be terminally ill or receiving palliative care for another condition only at the time of recruitment.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Between- and within- person variability of point-of-care NP is measured using point-of-care NT-proBNP test results at baseline, 6 months, 12 months, and routine visits for heart failure.
- Secondary Outcome Measures
Name Time Method