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[18F] AldoView PET/CT-guided Precision Partial Adrenalectomy in Unilateral Solitary Aldosterone-Producing Adenoma for Efficacy Evaluation: A China, Multicentre, Prospective, Proof-of-concept Trial

[18F] AldoView PET/CT-guided Precision Partial Adrenalectomy in Unilateral Solitary Aldosterone-Producing Adenoma for Efficacy Evaluation: A China, Multicentre, Prospective, Proof-of-concept Trial - PREPARE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123153
Enrollment
Unknown
Registered
2026-04-22
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Primary aldosteronism

Interventions

Prospective cohort (precise partial adrenalectomy group):[18F] Aldoview PET/CT functional imaging indicated partial adrenalectomy for unilateral solitary aldosterone-producing adenoma
Retrospective cohort (unilateral total adrenalectomy group):None

Sponsors

Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Prospective cohort: 1. Hypertensive patients aged 18-75 years; 2. Diagnosed with primary aldosteronism; 3. Thin-layer enhanced CT of the adrenal glands indicates unilateral adrenal lesion and AVS suggests the same side as the dominant side; 4. [18F] Aldoview PET/CT indicates a single positive nodule on one side, with no limit on nodule size; 5. Patients willing to undergo surgical treatment; 6. Willing and able to follow the study protocol and follow-up, and sign the informed consent form. Retrospective cohort: 1. Hypertensive patients aged 18-75 years; 2. Diagnosed with primary aldosteronism; 3. Thin-layer enhanced CT of the adrenal glands indicates unilateral adrenal lesion and AVS suggests the same side as the dominant side; 4. [18F] Aldoview PET/CT indicates a single positive nodule on one side, with no limit on nodule size; 5. Underwent unilateral adrenalectomy; 6. Willing and able to follow the study protocol and follow-up, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: Prospective cohort: 1.Patients with other common secondary hypertension, such as renal artery stenosis, renal parenchymal hypertension, pheochromocytoma, hypercortisolism, etc.; 2. Patients with malignant tumors or functional disorders of the heart, liver, kidney, and severe physical diseases who cannot tolerate surgery; 3. Patients with severe mental disorders or cognitive impairments who cannot cooperate with the study; 4. Patients who have undergone adrenal surgery before; 5. Patients with adrenal cortical insufficiency requiring hormone replacement therapy; 6. Patients who have been using glucocorticoids for a long time and cannot discontinue the use. Retrospective cohort: 1. Patients with other common secondary hypertension, such as renal artery stenosis, renal parenchymal hypertension, pheochromocytoma, hypercortisolism, etc.; 2. Patients with malignant tumors or functional disorders of the heart, liver, kidney, and severe physical diseases; 3. Patients with severe mental disorders or cognitive impairments who cannot cooperate with the study; 4. Patients who have undergone adrenal surgery before in the context of unilateral adrenal resection; 5. Patients with adrenal cortical insufficiency requiring hormone replacement therapy; 6. Patients who have been using glucocorticoids for a long time and cannot discontinue the use.

Design outcomes

Primary

MeasureTime frame
Biochemical complete success;Clinical complete success;

Secondary

MeasureTime frame
Clavien-Dindo degree;The incidence of postoperative adrenal cortical insufficiency;Biochemical partial success;Clinical partial success;

Countries

China

Contacts

Public ContactLongfei Liu

Xiangya Hospital, Central South University

longfei_liu@csu.edu.cn+86 158 7486 9636

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026