Primary Aldosteronism Due to Adrenal Hyperplasia (Bilateral) Clinical Trial
— SAAE-BIHOfficial title:
Efficacy and Safety of Percutaneous Superselective Adrenal Arterial Embolization in the Treatment of Primary Aldosteronism With Bilateral Idiopathic Hyperaldosteronism: A Prospective Cohort Study
Verified date | December 2021 |
Source | Second Affiliated Hospital of Nanchang University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The most common two subtypes of primary aldosteronism (PA ) are aldosterone producing adenoma (APA) and bilateral idiopathic hyperaldosteronism (IHA). Mineralocorticoid receptor (MR) antagonists is the main treatment for bilateral IHA, because of its side effects, the treatment compliance of those patients is poor. Hence, an alternative therapy is needed in such cases. We hypothesized that superselective adrenal artery embolization (SAAE) could be a suitable alternative approach. To our knowledge, SAAE has so far not been applied to treat bilateral IHA. This study aimed to evaluate the efficacy and safety of SAAE in the treatment of PA patients with bilateral IHA.
Status | Enrolling by invitation |
Enrollment | 50 |
Est. completion date | December 31, 2022 |
Est. primary completion date | December 31, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - (1) Age 18-60 years old, regardless of gender; (2) After strict drug elution, it met the diagnostic criteria of primary aldosteronism, and bilateral idiopathic aldosteronism was confirmed by adrenal venous sampling; (3) Blood pressure conditions meet one of the following: 1) Office blood pressure = 140/90mmHg; 2) Ambulatory blood pressure monitoring:whole day blood pressure > 130/80 mmHg or daytime blood pressure > 135/85 mmHg; (4) Adrenal CT showed adrenal hyperplasia, nodules or no obvious morphological abnormalities; (5) The course of hypertension is more than 6 months; (6) The patient or his legal representative shall sign the written informed consent approved by the ethics committee before screening. Exclusion Criteria: - (1) Primary hypertension or secondary hypertension with other causes; (2) A woman who is pregnant or lactating, or has a birth plan in the next year; (3) There are serious organic diseases, especially liver and kidney dysfunction; (4) Severe allergy to contrast medium; (5) Other serious organic diseases, life expectancy < 12 months; (6) Adrenal CT showed adenoma. (7) Patients are enrolled or want to participate in other clinical studies. During the enrollment study, the results of this study will be affected. |
Country | Name | City | State |
---|---|---|---|
China | the Second Affiliated Hospital of Nanchang University | Nanchang | Jiagxi |
Lead Sponsor | Collaborator |
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Second Affiliated Hospital of Nanchang University |
China,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Ambulatory blood pressure monitoring | 24-hour ambulatory blood pressure monitor | one month after SAAE | |
Primary | Office blood pressure | sphygmomanometer | one month after SAAE | |
Secondary | plasma aldosterone | reagent | one month after SAAE | |
Secondary | potassium levels | reagent | one month after SAAE | |
Secondary | adverse events | follow-up | one month after SAAE |
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