Double Pet Project : A Comparison Between 11C-Acetate and 11C-acetoacetate Heart and Kidney Uptake

NCT ID: NCT05238805

Last Updated: 2023-01-18

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

COMPLETED

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-03-14

Study Completion Date

2022-08-14

Brief Summary

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The objective of this study is to make a comparison between 11C-acetate and 11C-Acetoacetate heart and kidney metabolism

Detailed Description

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Healthy people will have two positron emission tomography scan to perform. One, with a 11C-Acetate Tracer and the other with 11C-Acetoacetate. The results will allow to determine if both tracers are used in a similar way but the organs and see if the investigators can use the already validated analyse method for acetate to make acetoacetate analysis

Conditions

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Ketoses, Metabolic

Study Design

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Allocation Method

NA

Intervention Model

SEQUENTIAL

Participants will have to perform 2 scans one after the other
Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Observational heart and kidney metabolism

Participants will have a PET scan with 11C-Acetate followed by a TEP Scan with 11C-Acetoacetate all in the same day.

Group Type OTHER

Observational heart and kidney on siemens TEP scan

Intervention Type RADIATION

Same as arm description

Interventions

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Observational heart and kidney on siemens TEP scan

Same as arm description

Intervention Type RADIATION

Eligibility Criteria

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Inclusion Criteria

* Aged between 18 and 55
* BMI between 18,5 and 28
* Healthy
* Normal value for blood pressure

Exclusion Criteria

* Taking drugs that could influence metabolism
* Diabetes or prediabetes
* Pregnancy or lactation
* Participation in a intensive sport program
* Being on a ketogenic diet
* Any clinical abnomally in prescreen blood sample
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Nestlé Health Science Spain

INDUSTRY

Sponsor Role collaborator

Université de Sherbrooke

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Research Center on Aging

Sherbrooke, Quebec, Canada

Site Status

Countries

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Canada

Other Identifiers

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2022-4540

Identifier Type: -

Identifier Source: org_study_id

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