3 registrations that name wheat Dextrin as a study arm and are recruiting or about to, as ClinicalTrials.gov listed them on Oct 20, 2026. Read each listing for its full criteria and current status.
Kymata never assesses eligibility. Each listing names its own criteria; only its study team can say whether someone can join. Trial doses are given under the trial's monitoring and are not a schedule for anyone outside it.
Filter 3 registrations
Status
Phase
3US sites across 3 states
1
2 to 4
5 to 19
20 or more
All 3 registrations
RecruitingNCT06852365
Combined Oral Contraceptive Pill and Resistance Starch
Phase 2
University of Pennsylvania
About 100 people
Started Jun 10, 2025
In plain words A Phase 2 study of wheat Dextrin in female participants 18 to 40, run by University of Pennsylvania. It plans to enroll about 100 people at 1 US site.
Women between ages of 18-40 years with BMI greater than or equal to 25 kg/m² to less than or equal to 48 kg/m² diagnosed with PCOS defined by the Rotterdam criteria based on a history of chronic anovulation (8 or fewer periods), androgen…
For women with more regular bleeding patterns, but who are suspected to be experiencing periodic anovulatory bleeding, a midluteal progesterone (P4) level less than 3ng/dL will be evidence of ovulatory dysfunction and qualify as…
Women with only hyperandrogenic PCOS phenotype (hyperandrogenism + one more criteria) will be included to decrease the heterogeneity of the cohort and as metabolic risks are increased in these women compared to normo-androgenic women with…
Subjects should be willing to avoid pregnancy for the entire duration of the study.
This study will enroll women with PCOS to study the effects of first line therapy, oral contraceptive pills, and then either 12 weeks of resistant starch or 12 weeks of placebo to explore if resistant starch improves cardiometabolic parameters or impacts gut dysbiosis compared to placebo.
Where, as registered
1 US site in 1 state.
RecruitingNCT07846254
The Effects of Daily Supplementation of a Soluble Fiber on the Fecal Microbiota in Volunteers.
No phase
Roquette Freres
About 100 people
Started Aug 31, 2026
In plain words A study of wheat Dextrin in people 18 to 60, run by Roquette Freres. It plans to enroll about 100 people at 1 US site.
Who it lists and where
Who the trial lists, as registered
Lists people 18 to 60; healthy volunteers accepted. Conditions: Healthy Volunteers.
Men and women aged ≥ 18 and ≤ 60 years;
Body mass index (BMI) ≥ 18 and ≤ 30 kg/m²;
With a usual normal intestinal transit (according to BSS). According to stool questionnaire completed between V0 and V1, mean of the 7 days of completion, maximum 3 stools / day and 3 stools/week minimum and with mean normal consistency
Good general and mental health according to the opinion of the investigator: no clinically significant and relevant abnormalities of medical history or physical examination;
3 more inclusion criteria and the exclusion criteria are on the listing.
What it tests, as registered
NUTRIOSE®; Active comparator
Registered summary
The effects of daily supplementation with NUTRIOSE® on the fecal microbiota. The study aims to evaluate the ability of NUTRIOSE® to support a beneficial modulation of the intestinal microbiota in healthy volunteers, compared with a placebo.
Where, as registered
1 US site in 1 state.
RecruitingNCT07756658
The Effects of Tyrosol and Creatine on Exercise Performance and Cognition in Healthy Adults
No phase
Applied Science & Performance Institute
About 60 people
Started Sep 4, 2026
In plain words A study of wheat Dextrin in male participants 20 to 55, run by Applied Science & Performance Institute. It plans to enroll about 60 people at 1 US site.
Who it lists and where
Who the trial lists, as registered
Lists male participants 20 to 55; healthy volunteers accepted. Conditions: Tyrosol; Creatine; Endurance Performance; Cognition; Mood.
Healthy males aged 20-55
Currently active (engaged in moderate to vigorous activity at least 2-days per week as defined by the American College of Sports Medicine Guidelines)
Estimated VO2 max greater than the 40th percentile of the population norm for age (assessed via ACSM guidelines, 2014).
Able to read and write in English
2 more inclusion criteria and the exclusion criteria are on the listing.
What it tests, as registered
Tyrosol; Creatine Monohydrate; Resistant Dextrin
Registered summary
This study will be a randomized, double-blind, placebo-controlled trial. It will be conducted over a 8-week intervention investigating the effects of creatine (5g Creatine monohydrate); placebo control (5g resistant dextrin), and a combination group containing both creatine and tyrosol (5g creatine monohydrate + 150mg tyrosol/day). Endurance, strength, cognition, and fatigue resistance will be examined through repeated strength and endurance testing (described below). The full summary is on the listing.