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Adrenal Artery Ablation for Primary Aldosteronism With Resistant Hypertension

Adrenal Artery Ablation Treats Primary Aldosteronism With Resistant Hypertension (AAA-RHT)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04345198
Enrollment
36
Registered
2020-04-14
Start date
2017-10-01
Completion date
2019-10-15
Last updated
2020-04-14

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

Conditions

Resistant Hypertension

Keywords

resistant hypertension; aldosteronism

Brief summary

Primary aldosteronism(PA) is the most common endocrine cause of resistant hypertension. Surgery and medicine are the main treatment for PA by the current guidelines. However,only a small part of patients with PA meet the surgical criteria, and most of them have to take spironolactone or other antihypertensive drugs for long time. On the other side, long-term inhibition of aldosterone receptor may cause hyperkalemia, male breast hyperplasia and other adverse reactions. Moreover, hyperaldosterone is still not corrected by spironolactone, which cause extensive cerebrovascular damages even though blood pressure and blood potassium had been normalized. With the development of adrenal vein sampling and adrenal ablation, the precise diagnosis and treatment of PA is possible. Selective adrenal artery ablation (AAA) was observed with significant decrease of blood aldosterone and blood pressure in patients with PA, which made it promissing that primary aldosteronism with resistant hypertension could be relieved by adrenal artery ablation.

Interventions

PROCEDUREAdrenal Artery Ablation

Intervention with adrenal artery ablation is performed in PA patients with resistant hypertension.

Sponsors

Third Military Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Male or female, age between 30-65 years old. * Primary aldosteronism with resistant hypertension. * Informed consent signed and agreed to participate in this trial.

Exclusion criteria

* Secodary hyertension due to other causes. * History of depression,schizophrenia or vascular dementia . * History of cardio-cerebral vascular events such as congestive heart failure, myocardial infarction or stroke within 3 months. * Hypohepatia (AST or AST is twice higher than the upper limit) or history of hepatitis or cirrhosis, hepatic encephalopathy. * Renal insufficiency ( serum creatinine is 1.5 times higher than the upper limit) or history of dialysis and nephritic syndrome. * Acute infections, tumor, severe arrhythmia, mental disorders, alcohol or medicine addiction. * Fertile woman without contraceptives. * Any surgical or medical conditions that significantly influence absorption, distribution, metabolism or excretion of the anti-hypertensive drugs. * Allergic to or have contraindication to the contrast agents and alcohol.

Design outcomes

Primary

MeasureTime frameDescription
Change of office systolic blood ptressure24 weeksChange of office systolic blood pressure compared with baseline after 24 weeks.

Secondary

MeasureTime frameDescription
Change of home systolic blood pressure24 weeksChange of home systolic blood pressure compared with baseline after 24 weeks.
Change of home diastolic blood pressure24 weeksChange of home diastolic blood pressure compared with baseline after 24 weeks.
Change of 24-h average systolic blood pressure24 weeksChange of 24-h average systolic blood pressure compared with baseline after 24 weeks.
Change of 24-h average diastolic blood pressure24 weeksChange of 24-h average diastolic blood pressure compared with baseline after 24 weeks.
Change of office dystolic blood pressure24 weeksChange of office dystolic blood pressure compared with baseline after 24 weeks.
Change of plasma adrenal hormones24 weeksChange of plasma aldosterone and cortisol compared with baseline after 24 weeks.
Change of plasma renin levels24 weeksChange of plasma renin levels compared with baseline after 24 weeks.
Change of blood electrolytes24 weeksChange of serum potassium, natrium, and chlorine compared with baseline after 24 weeks.
Change of serum creatinine24 weeksChange of serum creatinine measured as umol/L compared with baseline after 24 weeks.
Change of DDD of anti-hypertensive regimen24 weeksChange of Defined Daily Dose (DDD) of anti-hypertensive regimen compared with baseline after 24 weeks.

Countries

China

Outcome results

None listed

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