Skip to content

Percutaneous Radiofrequency Renal Sympathetic Denervation- Evaluation of results

Percutaneous Radiofrequency Renal Sympathetic Denervation- Evaluation of results - Renal Sympathetic Denervation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON36656
Enrollment
10
Registered
2011-04-22
Start date
2011-05-19
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

high blood pressure hypertension

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: -Age > 18 years en

Exclusion criteria

Exclusion criteria: - Secondary causes of hypertension - Renal Artery stenosis - Suboptimal dosage of antihypertensives - non-complicance -white coat hypertension -pregnancy -GFR

Design outcomes

Primary

MeasureTime frame
- observation of effectiveness renal sympathetic denervation (decrease in blood pressure) -observation of safety of renal sympathetic denervation (adverse events procedure)

Secondary

MeasureTime frame
- decrease in sympathetic tone

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)