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Trial · NCT02811289

Pharmacological Activation of Brown Adipose Tissue Metabolism

NCT02811289, Not applicable, Completed, Université de Sherbrooke

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Pharmacological Activation of Brown Adipose Tissue Metabolism. Trials, record NCT02811289. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02811289

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Pharmacological Activation of Brown Adipose Tissue Metabolism
NCT number
NCT02811289
Status
Completed
Phases
Not applicable
Enrollment
22 participants, actual
Lead sponsor
Université de Sherbrooke
Conditions
Type 2 Diabetes
Interventions
Mirbetriq (Mirabegron), cold exposure, injection of 18FDG, injection of 11C-acetate, [3-3H]-glucose, [U-13C]-palmitate, 2H-Glycerol
First posted
2016-06-23
Last updated
2018-08-22

Source ClinicalTrials.gov

Registered outcomes12

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryBAT net glucose uptake2 yearswill be assessed using i.v. injection of 18FDG with sequential dynamic PET/CT scanning.
PrimaryBAT oxidative metabolism2 yearswill be determined using i.v. injection of 11C-acetate during dynamic PET/CT scanning
PrimaryBAT volume of metabolic activity2 yearswill be determined using a total body CT (16 mA) followed by a PET acquisition.
Primarywhole body organ glucose partitioning2 yearswill be determined using a total body CT (16 mA) followed by a PET acquisition be determined using a total body CT (16 mA) followed by a PET acquisition
Secondarylipolysis rate2 yearswill be measured using i.v. administration of \[13C\]-palmitate and \[2H\]-glycerol, using steele's non steady state equations
SecondaryGlucose appearance rate2 yearswill be determined using \[3-3H\]-glucose
SecondaryEnergy expenditure2 yearswill be determined by indirect calorimetry from VO2 and VCO2 (Vmax29n, Sensormedics)
SecondaryInsulin sensitivity2 yearswill be determined using the HOMA-IR (based on fasting insulin and glucose levels)
SecondaryInsulin secretion rate2 yearswill be assessed using deconvolution of plasma C-peptide with standard C-peptide kinetic parameters
Secondaryβ-cell function2 yearswill be assessed by calculation of the disposition index (DI) that is insulin secretion in response to the ambient insulin sensitivity.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
32755608DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02811289

GET https://conductscience.org/api/trials/v1/NCT02811289/registered