Clinical trials

5

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Assessing Changes in the Gut Microbiome of Non-Gastrointestinal Disordered Subjects Before and After Oral Prebiotic Supplementation Using the SIMBA Capsule

This is a randomized, double-blind, placebo-controlled, parallel-group clinical study. The primary objective is to assess the changes in the small intestinal (SI) metagenomic profile of healthy participants without any known gastrointestinal disorders from baseline to endpoint in response to the prebiotic intervention (FiberSmart). The study population are adults (n=30) who will ingest either the FiberSmart or a matched Placebo daily for 21 days. Both products will be referred to as the Investigational Product (IP) in the study procedures section. While prebiotics are widely used for gut health, their specific impact on the small intestinal ecosystem remains largely uncharacterized compared to the large intestine. Understanding their impact on the upper GI tract can lead to new insights into their mechanisms of action. Given the critical role of the small intestine in metabolism and immunity, the study utilizes the SIMBA capsule to measure novel changes in the small intestine along with traditional measurements from stool samples.

Participants needed: 30
Trial details
Phase: Phase 4Age: 19-40Biological sex: MaleType: InterventionalSponsor: Nimble Science Ltd.Updated: Apr 13, 2026Locations: 1
Eligibility criteria

Aged 19-40 years old at the inclusion of the study, both female and male subject... [+5]

Use of any prescription medication within 14 days prior to the start of the stud... [+13]

Status: Not yet recruiting

Assessing Gut Microbiome Changes Before and After an Oral Nutritional Supplement Intake Using the SIMBA Capsule in Diabetic Participants

This is a single-arm interventional clinical study, the primary objective is to assess the changes in the small intestinal (SI) metagenomic profile of in diabetic participants from baseline to midpoint and endpoint in response to the ONS intervention. The study population is Type 2 Diabetes (T2D) participants (n=30) who will ingest an Oral Nutritional Supplement (ONS) .

Participants needed: 30
Trial details
Phase: Phase 1Age: 40-65Biological sex: AllType: InterventionalSponsor: Nimble Science Ltd.Updated: Aug 11, 2025Locations: 1
Eligibility criteria

Aged 40-65 years old at the inclusion of the study, both female and male subject... [+11]

Confirmed type 1 diabetes and/or had a history of diabetic ketoacidosis. [+32]

Status: Recruiting

The Safety And Efficacy Of A Probiotic Intervention On Lactulose Hydrogen Breath Test-Positive Patients And Related Gastrointestinal Symptoms

The goal of this study is to test the effect of a probiotic formulation on gastrointestinal symptoms, gut and small intestine microbiota in participants suffering from small intestinal bacterial overgrowth (SIBO). Two doses of probiotic will be evaluated against placebo.

Participants needed: 105
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Nimble Science Ltd.Updated: Apr 29, 2025Locations: 1
Eligibility criteria

Aged 18-65 years old at the inclusion of the study, both female and male subject... [+6]

History of less than three (3) bowel movements per week. [+27]

Status: Recruiting

Evaluation of the SIMBA Capsule for Small Intestinal Dysbiosis

The SIMBA Capsule is a small, single-use, ingestible capsule that allows for the non-invasive sampling of small bowel contents using purely mechanical means. The study will compare the microbial and metabolomics analysis from the sample collected with the capsule series, to same-participant symptom questionnaires and stool microbial analysis.

Participants needed: 300
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Nimble Science Ltd.Updated: Apr 15, 2025Locations: 1
Eligibility criteria

1. Aged between 18 and 80 years. [+5]

Known disease which, in the investigator's opinion, would lead to intestinal str... [+10]

Status: Not yet recruiting

Assessing the Safety of an IGY Supplement on the Gut Microbiome

This study is to evaluate whether Muno-IgY is effective in enhancing immune health among adults over a six week period.

Participants needed: 20
Trial details
Phase: Phase 1Age: 18-65Biological sex: AllType: InterventionalSponsor: Nimble Science Ltd.Updated: Nov 22, 2024Locations: 1
Eligibility criteria

Aged 18-65 years old at the inclusion of the study, both female and male subject... [+3]

Use of regular prescription medications, including antihypertensives, anti-infla... [+19]