Clinical trial • Not applicable • Endocrinology

Para-chloro-2-[18F]fluoroethyl-etomidate for Primary aldosteronism

Not applicable trial of Para-chloro-2-[18F]fluoroethyl-etomidate for Primary aldosteronism. 12 participants.

Overview

Trial Therapeutic Area
Endocrinology
Trial Disease
Primary aldosteronism
Trial Stage
Not applicable
Drug Modality
Radiopharmaceutical

Key dates

Initial CTIS Submission Date
14-02-2024
First CTIS Authorization Date
05-06-2024

Trial design

Not applicable trial across 1 site in Netherlands.

Target Sample Size
12

Eligibility

Recruits 12 No vulnerable population selected.

Vulnerable Population
No vulnerable population selected

Recruitment

Planned Sample Size
12
Recruitment Window Months
25

Geography

Total Number Of Sites
1
Total Number Of Participants
12

Netherlands

Earliest CTIS Part Ii Submission Date
06-05-2024
Latest Decision Or Authorization Date
05-06-2024
Processing Time Days
30
Number Of Sites
1
Number Of Participants
12

Sites

Site Name
University Medical Center Groningen
Department Name
Internal Medicine - Endocrinology
Principal Investigator Name
Michiel Kerstens
Principal Investigator Email
m.n.kerstens@umcg.nl
Contact Person Name
Michiel Kerstens
Contact Person Email
m.n.kerstens@umcg.nl
Number Of Participants
12

Sponsor

Primary sponsor

Full Name
Universitair Medisch Centrum Groningen
Organisation Type
Hospital/Clinic/Other health care facility
Country Of Registered Address
Netherlands

Investigational products

Investigational Product Name
Para-chloro-2-[18F]fluoroethyl-etomidate ([18F]CETO)
Active Substance
Para-chloro-2-[18F]fluoroethyl-etomidate
Modality
Radiopharmaceutical

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