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Neurological Impacts of Artificial Sweeteners in the Context of Diet Sodas

Beth Israel Lahey Health logo

Beth Israel Lahey Health

Status

Completed

Conditions

Obesity

Treatments

Behavioral: Carbonated Water
Behavioral: Regular soda
Behavioral: diet soda

Study type

Interventional

Funder types

Other

Identifiers

NCT04048681
2019P000649

Details and patient eligibility

About

This study seeks to determine whether artificial sweeteners in the context of diet soda may alter the brain's response to food cues and thus impact appetite.

Enrollment

5 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Men and women who are 18-65 years old, with a BMI >30kg/m2.

Exclusion criteria

  • Unable or unwilling to participate in the study for any reason
  • Metal in the body or other safety concerns which makes patient unable to have an MRI
  • Pregnant women will be excluded to protect the fetus against potential effects of a non-medically required MRI on fetal development and difficulty of measuring accurate BMI.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

5 participants in 3 patient groups, including a placebo group

Diet Soda
Experimental group
Description:
12oz can of Diet Coke
Treatment:
Behavioral: diet soda
Soda
Active Comparator group
Description:
12oz can of Coke
Treatment:
Behavioral: Regular soda
Carbonated Water
Placebo Comparator group
Description:
12oz can of carbonated (unflavored) water
Treatment:
Behavioral: Carbonated Water

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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