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The Effect of Renal Denervation on Renal Flow in Humans

The Effect of Renal Denervation on Renal Flow in Humans

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01848314
Enrollment
15
Registered
2013-05-07
Start date
2013-04-30
Completion date
2014-09-30
Last updated
2015-06-08

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

Conditions

Hypertension

Brief summary

Many studies have studied the effect and safety of renal denervation. However, it remains unknown what the exact mechanism behind renal denervation is. It can be hypothesized that a difference in renal blood flow occurs after treatment. In the light of this ignorance, current study will investigate whether renal denervation leads to a difference in renal blood flow after treatment with renal denervation.

Interventions

PROCEDURERenal Denervation

Flowmeasurements will be performed before and after renal denervation

Sponsors

UMC Utrecht
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Individual is scheduled to undergo renal denervation as standard patient care for resistant hypertension. * Individual is diagnosed with resistant hypertension. Secondary causes and a white coat hypertension are actively excluded. * Individual is ≥18 years of age. * Individual agrees to have all study procedures performed, and is competent and willing to provide written informed consent to participate in this clinical study.

Exclusion criteria

* Individual is excluded from treatment with pRDN . * Individual has an estimated glomerular filtration rate (eGFR) of \<30mL/min/1.73m2, using the MDRD calculation. * Individual has experienced a myocardial infarction, unstable angina pectoris, or a cerebrovascular accident within 6 months of the screening visit, or has widespread atherosclerosis, with documented intravascular thrombosis or unstable plaques. * Individual has any serious medical condition, which in the opinion of the investigator, may adversely affect the safety and/or effectiveness of the participant or the study (i.e., patients with clinically significant peripheral vascular disease, abdominal aortic aneurysm, bleeding disorders such as thrombocytopenia, haemophilia or significant anaemia). * Individual is pregnant, nursing or planning to be pregnant. * Individual has a known, unresolved history of drug use or alcohol dependency, lacks the ability to comprehend or follow instructions, or would be unlikely or unable to comply with study follow-up requirements.

Design outcomes

Primary

MeasureTime frame
Change in microvascular resistanceWithin 30 minutes after renal denervation

Secondary

MeasureTime frame
change in average flow velocitywithin 30 minutes after renal denervation

Other

MeasureTime frame
safety of measurementwithin 24 hour after renal denervation

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026