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Recruiting NCT07318077

NCT07318077 Radicle GI Health DBG: A Study Assessing the Impact of Health and Wellness Products on GI Health and Related Health Outcomes

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Clinical Trial Summary
NCT ID NCT07318077
Status Recruiting
Phase
Sponsor Radicle Science
Condition Belly Pain
Study Type INTERVENTIONAL
Enrollment 825 participants
Start Date 2026-01-06
Primary Completion 2027-01-13

Eligibility & Interventions

Sex All sexes
Min Age 21 Years
Max Age 105 Years
Study Type INTERVENTIONAL
Interventions
GI Health Product Placebo ControlGI Health Active Product 1GI Health Active Product 2

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 825 participants in total. It began in 2026-01-06 with a primary completion date of 2027-01-13.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Radicle GI Health DBG: A randomized, double-blind, placebo-controlled study assessing the impact of health and wellness products on GI health and related health outcomes.

Eligibility Criteria

Inclusion Participants must meet all the following criteria: * Adults, at least 21 years of age at the time of electronic consent, inclusive of all ethnicities, races, and gender identities * Assigned sex at birth will determine sex-specific recruitment and surveys (male vs female) employed, when needed * Resides in the United States * Has the opportunity for at least 30% improvement in their primary health outcome * Expresses a willingness to take a study product and not know the product identity (active or placebo) until the end of the study Exclusion Individuals who report any of the following during screening may be excluded from participation: * Report being pregnant, trying to become pregnant, or breastfeeding * Unable to provide a valid US shipping address and mobile phone number * Unable to verify their identity during consent using Veriff * Reports current enrollment in another clinical trial * Reports being a heavy drinker (defined as drinking 3 or more alcoholic beverages per day) * Unable to read and understand English at approx. a 7th grade level * Reports a current and/or recent (up to 3 months ago) major illness and/or surgery that poses a known, significant safety risk. * Reports a diagnosis of cardiac dysfunction, liver or kidney disease that presents a known contraindication and/or a significant safety risk with any of the study product ingredients. * NYHA Class III or IV congestive heart failure, atrial fibrillation, uncontrolled arrhythmias, cirrhosis, end-stage liver disease, stage 3b or 4 chronic kidney disease, or kidney failure * Reports taking medications that have a well-established moderate or severe interaction, posing a substantial safety risk with any of the study product ingredients. * Anticoagulants, antihypertensives, anxiolytics, antidepressants, chemotherapy, immunotherapy, sedative hypnotics, seizure medications, medications that warn against grapefruit consumption, corticosteroids at doses greater than 5 mg per day, diabetic medications, oral anti-infectives (antibiotics, antifungals, antivirals) to treat an acute infection, antipsychotics, MAOIs, or thyroid products * Reports current use of the primary ingredient(s) and/or similar product(s) to the active study product(s) that may limit the effects of the study products and/or pose a safety risk * Lack of reliable daily access to the internet

Contact & Investigator

Central Contact

Study Manager

✉ studymgmt@radiclescience.com

📞 858-779-0086

Principal Investigator

Susan Hewlings

PRINCIPAL INVESTIGATOR

Radicle Science

Frequently Asked Questions

Who can join the NCT07318077 clinical trial?

This trial is open to participants of all sexes, aged 21 Years or older, up to 105 Years, studying Belly Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07318077 currently recruiting?

Yes, NCT07318077 is actively recruiting participants. Contact the research team at studymgmt@radiclescience.com for enrollment information.

Where is the NCT07318077 trial being conducted?

This trial is being conducted at Del Mar, United States.

Who is sponsoring the NCT07318077 clinical trial?

NCT07318077 is sponsored by Radicle Science. The principal investigator is Susan Hewlings at Radicle Science. The trial plans to enroll 825 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology