Sequential Combined Versus Single-Strategy Adrenal Venous Sampling for Primary Aldosteronism(SCOPE)

NCT ID: NCT07298954

Last Updated: 2025-12-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

456 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-12-25

Study Completion Date

2028-12-31

Brief Summary

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This study is a prospective, multicenter, randomized clinical trial aimed to compare the impact of three AVS diagnostic strategies on the clinical outcomes of patients with primary aldosteronism. The strategies include sequential combined AVS (non-ACTH-stimulated followed by ACTH-stimulated AVS), non- ACTH-stimulated AVS alone, and ACTH-stimulated AVS alone. The findings of this study will provide critical evidence for the clinical practice standards of AVS.

Detailed Description

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This is a prospective, multicenter, randomized controlled clinical trial. This study will be led by the First Affiliated Hospital of Chongqing Medical University, with Chuxiong Yi Autonomous Prefecture People's Hospital, the First Affiliated Hospital of Kunming Medical University, and the First Affiliated Hospital of Nanchang Medical University serving as collaborating centers. According to the inclusion and exclusion criteria, eligible patients with confirmed primary aldosteronism (PA) will be enrolled and randomly assigned in a 1:1:1 ratio to one of the following groups: sequential combined AVS, non-ACTH-stimulated AVS alone, and ACTH-stimulated AVS alone. These stratifications will guide clinical treatment decisions, either surgical therapy or medical therapy, and patients will be followed to evaluate their clinical outcomes. The primary outcome is the treatment response rate at 6-month follow-up, which will be compared among the three groups.

Conditions

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Primary Aldosteronism

Keywords

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Primary Aldosteronism Adrenal venous sampling sequential combined AVS non-ACTH-stimulated ACTH-stimulated AVS complete biochemical remission rate

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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sequential combined AVS

non-ACTH-stimulated followed by ACTH-stimulated AVS

Group Type EXPERIMENTAL

sequential combined AVS

Intervention Type DIAGNOSTIC_TEST

non-ACTH-stimulated followed by ACTH-stimulated AVS

non-ACTH-stimulated AVS

non-ACTH-stimulated AVS

Group Type NO_INTERVENTION

No interventions assigned to this group

ACTH-stimulated AVS

ACTH-stimulated AVS

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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sequential combined AVS

non-ACTH-stimulated followed by ACTH-stimulated AVS

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Fully understand the study process, voluntarily agree to participate, and sign informed consent.
* Diagnosed with primary aldosteronism. # Age 18-70 years with hypertension, any sex.

Exclusion Criteria

* Patients for whom AVS can be bypassed: Typical BPA (normal serum potassium and plasma aldosterone concentration (PAC) \< 110 pg/mL, eligible for direct medical therapy); Typical UPA (PAC ≥ 200 pg/mL, plasma renin concentration (PRC) ≤ 5 μIU/mL, spontaneous hypokalemia, unilateral adrenal adenoma ≥ 1 cm with normal contralateral adrenal on CT or 68Ga-Pentixafor PET-CT indicating unilateral functional tumor, eligible for direct surgery);
* Refusal of AVS or surgery, or contraindication to surgery.
* Allergy to ACTH or contrast agents.
* Combined with autonomous cortisol secretion (1 mg overnight dexamethasone suppression test cortisol ≥ 50 nmol/L).
* Early-onset hypertension (\<20 years) with hypokalemia and family history, suggestive of familial hyperaldosteronism or Liddle syndrome.
* Imaging cannot exclude pheochromocytoma or adrenocortical carcinoma (nodule ≥ 4 cm, CT ≥ 20 HU, or MRI suggestive).
* Active malignancy.
* Previous adrenal surgery.
* Chronic glucocorticoid use that cannot be discontinued.
* Adrenal insufficiency requiring hormone replacement.
* Pregnancy or breastfeeding; history of alcohol or substance abuse, or inability to cooperate due to psychiatric disorders.
* NYHA class III-IV heart failure or hospitalization for worsening heart failure in the past 3 months, stroke or acute coronary syndrome in past 3 months, severe anemia (Hb \< 60 g/L), severe liver or renal disease (ALT ≥ 3×upper limit; eGFR \<30 mL/min/1.73 m2 or dialysis), systemic inflammatory response syndrome (SIRS), poorly controlled diabetes (FBG ≥ 13.3 mmol/L), severe obesity (BMI ≥ 35 kg/m2), untreated aneurysm, or other conditions severely interfering with study participation.
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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First Affiliated Hospital of Kunming Medical University

OTHER

Sponsor Role collaborator

The First Affiliated Hospital of Nanchang University

OTHER

Sponsor Role collaborator

The People's Hospital of Chuxiong Yi Autonomous Prefecture

UNKNOWN

Sponsor Role collaborator

Shumin Yang

OTHER

Sponsor Role lead

Responsible Party

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Shumin Yang

Primary investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Shumin Yang

Role: STUDY_CHAIR

the Chongqing Primary Aldosteronism Study (CONPASS) Group

Locations

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The First Affilated Hospital of Chongqing Medical University

Chongqing, , China

Site Status RECRUITING

Countries

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China

Central Contacts

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Shumin Yang

Role: CONTACT

Phone: +86 023-89011552

Email: [email protected]

Facility Contacts

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Shumin Yang

Role: primary

References

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Other Identifiers

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SCOPE PA

Identifier Type: -

Identifier Source: org_study_id