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A Single Group Study to Evaluate the Efficacy of Bye Bye Bloat Capsules in Relieving Bloating and Promoting Healthy Digestion.

A Single Group Study to Evaluate the Efficacy of Bye Bye Bloat Capsules in Relieving Bloating and Promoting Healthy Digestion.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06516744
Enrollment
40
Registered
2024-07-24
Start date
2024-02-08
Completion date
2024-04-20
Last updated
2024-07-24

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

Conditions

Digestion, Digestive Health

Keywords

Gastrointestinal Symptoms, Hormonal Bloating, Capsule Supplement

Brief summary

This virtual single-group study aims to evaluate the efficacy of Bye Bye Bloat Capsules in relieving hormonal and food-related bloating and promoting healthy digestion. The study will last 4 weeks, involving 40 female participants aged 18+ who will take two capsules after meals and during times of bloating. Measurements and questionnaires will be completed at Baseline, first use, Week 2, and Week 4.

Interventions

DIETARY_SUPPLEMENTBye Bye Bloat Capsules

Bye Bye Bloat Capsules contain the following ingredients: Organic Fenugreek Seed Powder, Organic Dandelion Root Powder, Organic Fennel Seed Powder, Organic Ginger Root Powder, Organic Parsley Leaf Powder, Amylase Complex, Protease Complex, Pepsin Complex, Lipase Complex, Bromelain Complex, Papain Complex. Other ingredients include Hypromellose Capsule, Maltodextrin, Microcrystalline Cellulose, and Magnesium Stearate. Participants will take 2 capsules immediately after eating at least 3 times a week and during times of hormonal bloating for 4 weeks.

Sponsors

Citruslabs
CollaboratorINDUSTRY
Love Wellness
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Women aged 18+ * Self-reported concerns with bloating after eating * Issues with hormonal bloating * Generally healthy without uncontrolled chronic diseases * Willing to avoid using digestive health remedies and other oral supplements during the study

Exclusion criteria

* Pre-existing chronic conditions preventing adherence to the protocol * Undergoing procedures related to digestive health * Started new medications or supplements targeting digestive health in the past 3 months * Severe allergic reactions requiring an Epi-Pen * Pregnant, breastfeeding, or attempting to conceive * Unwilling to follow the study protocol * Recent surgeries or planned surgeries during the study * Diagnosed gastrointestinal disorders * Recent changes in hormonal birth control use

Design outcomes

Primary

MeasureTime frameDescription
Reduction in BloatingBaseline, first use, Week 2, and Week 4Evaluation of parameters associated with hormonal and food-related bloating through self-reported questionnaires taken at Baseline, first use, Week 2, and Week 4.

Secondary

MeasureTime frameDescription
Improvement in Digestion and Mental Well-beingBaseline, first use, Week 2, and Week 4Assessment of changes in participant perception of digestion, gas, mental health, and well-being associated with bloating through self-reported questionnaires taken at Baseline, first use, Week 2, and Week 4.

Countries

United States

Outcome results

None listed

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