The Renin Angiotensin System in Essential Hypertension
| ISRCTN | ISRCTN12415112 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN12415112 |
| Protocol serial number | N0236102657 |
| Sponsor | Record Provided by the NHSTCT Register - 2006 Update - Department of Health |
| Funders | St George's Healthcare NHS Trust (UK), No External Funding, NHS R&D Support Funding (UK) |
- Submission date
- 29/09/2006
- Registration date
- 29/09/2006
- Last edited
- 11/10/2017
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Circulatory System
Plain English summary of protocol
Not provided at time of registration
Contact information
Scientific
Blood Pressure Unit
Dept of Physiological Medicine
St George's Hospital Medical School
Cranmer Terrace
London
SW17 0RE
United Kingdom
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised crossover trial |
| Secondary study design | Randomised cross over trial |
| Study type | Participant information sheet |
| Scientific title | The Renin Angiotensin System in Essential Hypertension |
| Study objectives | To determine and compare the effects of enalapril on sodium balance, atrial pressure and the renin angiotensin aldosterone system in humans. |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Cardiovascular: Essential hypertension |
| Intervention | Randomised crossover trial |
| Intervention type | Other |
| Primary outcome measure(s) |
This research is based on the increasing evidence that blockade of the renin-angiotensin-aldosterone system has benefits additional to a fall in blood pressure. There are two major ways of blocking the renin-angiotensin system (RAS), either by inhibiting the enzyme that generates angiotensin II or by blocking the angiotensin receptor, that medicates most of the actions of angiotensin II on its target tissues. |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 30/09/2005 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 22 |
| Key inclusion criteria | 11 subjects and 11 controls |
| Key exclusion criteria | Does not meet inclusion criteria |
| Date of first enrolment | 03/12/2001 |
| Date of final enrolment | 30/09/2005 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
SW17 0RE
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Participant information sheet | Participant information sheet | 11/11/2025 | 11/11/2025 | No | Yes |
Editorial Notes
11/10/2017: No publications found, verifying study status with principal investigator.