Primary Aldosteronism and Surgically Curable Forms in Hypertension Patients Using 11C-Metomidate
Primary Purpose
Primary Aldosteronism, Primary Aldosteronism Due to Aldosterone Producing Adenoma
Status
Completed
Phase
Early Phase 1
Locations
Singapore
Study Type
Interventional
Intervention
11C-Metomidate PET/CT Scan
Sponsored by
About this trial
This is an interventional diagnostic trial for Primary Aldosteronism focused on measuring 11-C Metomidate PET/CT, Hypertension, Adrenalectomy, Adrenal Vein Sampling, Subtyping
Eligibility Criteria
Inclusion Criteria:
• Primary aldosteronism, as defined in Endocrine Society Guidelines 2016, with positive confirmatory test (post-salt loading aldosterone >140pmol/L); or hypokalemia with undetectable renin levels and aldosterone >550pmol/L.
Exclusion Criteria:
- Inability to provide written informed consent
- < 21 years or > 70 years
- Chronic renal failure of Stage 3b or greater severity
- Severe or terminal medical condition(s)
- Contraindications to isotope scanning or CT Scan
- Contraindication to ingestion of corticosteroids
Sites / Locations
- Changi General Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Single Arm
Arm Description
All patients will undergo standard-of-care investigations (CT imaging of adrenals and AVS) and the research test (11C-metomidate PET-CT) with a dose of 150 - 300 Megabecquerel (MBq) (11C-metomidate) to identify functional unilateral adrenal disease.
Outcomes
Primary Outcome Measures
Cure of Primary Aldosteronism Post-Adrenalectomy
Percentage of patients accurately identified with unilateral PA (determined by post-surgery biochemical cure) using 11C-metomidate PET/CT compared to percentage of patients accurately identified with unilateral PA (determined by post-surgery biochemical cure) using AVS
Secondary Outcome Measures
Clinical Diagnosis of Unilateral Primary Aldosteronism
Percentage of patients accurately identified with unilateral PA (determined by clinical diagnosis made by multidisciplinary team) using 11C-metomidate PET/CT compared to percentage of patients accurately identified with unilateral PA (determined by clinical diagnosis made by multidisciplinary team) using AVS
Cost-Effectiveness of Diagnostic Test
Cost-Effectiveness of Diagnostic Test to identify unilateral PA
Full Information
NCT ID
NCT03990701
First Posted
December 19, 2018
Last Updated
May 28, 2021
Sponsor
Changi General Hospital
Collaborators
National University Health System, Singapore, Clinical Imaging Research Centre, Singapore General Hospital, Tan Tock Seng Hospital, Khoo Teck Puat Hospital, Ng Teng Fong General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03990701
Brief Title
Primary Aldosteronism and Surgically Curable Forms in Hypertension Patients Using 11C-Metomidate
Official Title
Primary Aldosteronism and Surgically Curable Forms in Hypertension Patients Using 11C-Metomidate
Study Type
Interventional
2. Study Status
Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
May 21, 2018 (Actual)
Primary Completion Date
March 30, 2021 (Actual)
Study Completion Date
March 30, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Changi General Hospital
Collaborators
National University Health System, Singapore, Clinical Imaging Research Centre, Singapore General Hospital, Tan Tock Seng Hospital, Khoo Teck Puat Hospital, Ng Teng Fong General Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
10% of patients with hypertension potentially have the treatable condition - primary aldosteronism. Primary aldosteronism (PA) is caused by either bilateral adrenal disease (~40%), managed with lifelong medications; or unilateral disease (~60%), cured with laparoscopic surgery (adrenalectomy). Unfortunately, many patients with curable hypertension remain undiagnosed and consequently develop cardiac disease and strokes. The difficulty with identifying curable unilateral disease is due to adrenal vein sampling (AVS): an invasive, and technically-difficult procedure, with inconclusive results in 50% of patients. An alternative novel imaging, 11C-metomidate Positron emission tomography-computed tomography (PET-CT), can detect adrenal tumors, and concurrently confirm their over-activity. It is non-invasive, non-operator-dependent, and can identify more patients with curable hypertension.
Investigators hypothesize that 11C-metomidate PET-CT can accurately identify patients with surgically-curable unilateral adrenal disease among hypertensive Asians with primary aldosteronism.
Detailed Description
25 patients with confirmed PA who are keen for a surgical cure if unilateral PA is confirmed, will undergo conventional tests, CT, AVS, as well as 11C-metomidate PET/CT.
Results will be reviewed and discussed at a multidisciplinary meeting, and patients with unilateral PA will be offered surgery. Patients will be reviewed 6 months post surgery to assess for cure of PA.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Aldosteronism, Primary Aldosteronism Due to Aldosterone Producing Adenoma
Keywords
11-C Metomidate PET/CT, Hypertension, Adrenalectomy, Adrenal Vein Sampling, Subtyping
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Model Description
11C-metomidate will be manufactured in Clinical Imaging Research Centre in compliance with good manufacturing practice using a General Electric Medical Systems PET trace 860 cyclotron. Non-contrast CT images will be acquired over the adrenal. After an intravenous injection of 11C-metomidate, PET images will be acquired within the first 45 min. Attenuation and decay-corrected images will be converted to standardized uptake value (SUV) maps through division by (injected activity per patient weight). The maximum SUV values over regions of interest will be determined for 10-min static images starting 35 min after the injection.
Masking
None (Open Label)
Allocation
N/A
Enrollment
25 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Single Arm
Arm Type
Experimental
Arm Description
All patients will undergo standard-of-care investigations (CT imaging of adrenals and AVS) and the research test (11C-metomidate PET-CT) with a dose of 150 - 300 Megabecquerel (MBq) (11C-metomidate) to identify functional unilateral adrenal disease.
Intervention Type
Combination Product
Intervention Name(s)
11C-Metomidate PET/CT Scan
Intervention Description
11C-Metomidate PET/CT imaging at Clinical Imaging Research Centre
Primary Outcome Measure Information:
Title
Cure of Primary Aldosteronism Post-Adrenalectomy
Description
Percentage of patients accurately identified with unilateral PA (determined by post-surgery biochemical cure) using 11C-metomidate PET/CT compared to percentage of patients accurately identified with unilateral PA (determined by post-surgery biochemical cure) using AVS
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Clinical Diagnosis of Unilateral Primary Aldosteronism
Description
Percentage of patients accurately identified with unilateral PA (determined by clinical diagnosis made by multidisciplinary team) using 11C-metomidate PET/CT compared to percentage of patients accurately identified with unilateral PA (determined by clinical diagnosis made by multidisciplinary team) using AVS
Time Frame
6 months
Title
Cost-Effectiveness of Diagnostic Test
Description
Cost-Effectiveness of Diagnostic Test to identify unilateral PA
Time Frame
6 months
Other Pre-specified Outcome Measures:
Title
Diagnostic criteria using 11C-Metomidate PET/CT
Description
To assess the cut-off level of SUVmax which offers the best sensitivity and specificity for lateralisation in 11C-metomidate PET-CT
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
• Primary aldosteronism, as defined in Endocrine Society Guidelines 2016, with positive confirmatory test (post-salt loading aldosterone >140pmol/L); or hypokalemia with undetectable renin levels and aldosterone >550pmol/L.
Exclusion Criteria:
Inability to provide written informed consent
< 21 years or > 70 years
Chronic renal failure of Stage 3b or greater severity
Severe or terminal medical condition(s)
Contraindications to isotope scanning or CT Scan
Contraindication to ingestion of corticosteroids
Facility Information:
Facility Name
Changi General Hospital
City
Singapore
ZIP/Postal Code
529889
Country
Singapore
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35703880
Citation
Puar TH, Khoo CM, Tan CJ, Tong AKT, Tan MCS, Teo AE, Ng KS, Wong KM, Reilhac A, O'Doherty J, Gomez-Sanchez CE, Kek PC, Yee S, Tan AWK, Chuah MB, Lee DHM, Wang KW, Zheng CQ, Shi L, Robins EG, Foo RSY; for the PA CURE investigators. 11C-Metomidate PET-CT versus adrenal vein sampling to subtype primary aldosteronism: a prospective clinical trial. J Hypertens. 2022 Jun 1;40(6):1179-1188. doi: 10.1097/HJH.0000000000003132.
Results Reference
derived
Learn more about this trial
Primary Aldosteronism and Surgically Curable Forms in Hypertension Patients Using 11C-Metomidate
We'll reach out to this number within 24 hrs