Cost-effectiveness of low salt diet in lowering blood pressure in Hong Kong Chinese
| ISRCTN | ISRCTN65375464 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN65375464 |
| Protocol serial number | 811028 |
| Sponsor | Hong Kong Health Services Research Fund (Hong Kong) |
| Funder | Hong Kong Health Services Research Fund (Hong Kong) |
- Submission date
- 14/10/2002
- Registration date
- 14/10/2002
- Last edited
- 01/07/2009
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Circulatory System
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr BMY Cheung
Scientific
Scientific
Department of Medicine
Faculty of Medicine
University of Hong Kong
-
-
Hong Kong
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study objectives | Not provided at time of registration |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | High blood pressure |
| Intervention | All patients will undergo a 4-week placebo run-in and drug washout phase. After baseline measurements, each patient will be randomised to conventional treatment or low sodium diet for 6 months. |
| Intervention type | Other |
| Primary outcome measure(s) |
Not provided at time of registration |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 01/09/2000 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Lower age limit | 18 Years |
| Sex | All |
| Key inclusion criteria | 1. Age between 18 and 75 inclusive 2. Patient has seated diastolic blood pressure between 90 and 110 mmHg inclusive; or seated systolic blood pressure of greater than 140 mmHg 3. Patient must be willing to give full informed consent |
| Key exclusion criteria | Does not meet inclusion criteria |
| Date of first enrolment | 01/10/1998 |
| Date of final enrolment | 01/09/2000 |
Locations
Countries of recruitment
- Hong Kong
Study participating centre
Department of Medicine
-
-
Hong Kong
-
Hong Kong
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |