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Artificially Sweetened Beverage Feeding Study

Artificially Sweetened Beverage Feeding Study

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04258345
Enrollment
0
Registered
2020-02-06
Start date
2021-07-31
Completion date
2021-07-31
Last updated
2020-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Disease

Brief summary

The aims of the study are to conduct a pre- and post- two week feeding study of artificial sweetened beverage consumption in middle-aged women. The study will also compare metabolic profiles before and after artificially sweetened beverage consumption.

Detailed description

The aims of the study are to: 1. To conduct a pre- and post- two week feeding study of Artificially Sweetened Beverage (ASB) in women. 2. To assess the general levels of ASB consumption. 3. To compare metabolic profiles before and after beverage consumption

Interventions

OTHERASB Feeding Study

Participants will undergo a washout period and then scheduled for blood draw after which ASB feeding period will begin followed by a second blood draw.

Sponsors

Albert Einstein College of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
40 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

• Healthy women

Exclusion criteria

• Having a history of diabetes or cardiovascular disease and any other health or chronic condition that precludes participation in the study.

Design outcomes

Primary

MeasureTime frameDescription
Change in artificial sweetener levels pre- and post- feedingtwo weeksChange in metabolites pre- and post-feeding

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026