- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT05157815
Study to Investigate the Effect of Dietary Fibre Supplementation on Long-term Glucose Control in Prediabetic Subjects
A Randomized, Double-blind, Placebo-controlled, Parallel Study to Investigate the Effect of 16 Weeks of Twice Daily Supplementation With Soluble Corn Fibre on Long Term Glucose Control in Prediabetic Subjects
The purpose of the study is to explore the potential metabolic health benefits of a dietary fibre intervention by using Soluble Fibre in a human intervention study in Healthy Obese Pre-diabetic participants over a period of 16 weeks with a focus on long term glucose control.
The hypothesis is that twice daily supplementation with Soluble Fibre over a period of 16 weeks will significantly improve long term glucose control in pre-diabetic participants.
Tutkimuksen yleiskatsaus
Tila
Ehdot
Interventio / Hoito
Opintotyyppi
Ilmoittautuminen (Odotettu)
Vaihe
- Ei sovellettavissa
Yhteystiedot ja paikat
Opiskeluyhteys
- Nimi: Ieva Laurie, PhD
- Puhelinnumero: +447900632410
- Sähköposti: IEVA.LAURIE@TATEANDLYLE.COM
Opiskelupaikat
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Cork, Irlanti
- Rekrytointi
- Atlantia Food Clinical Trials
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Päätutkija:
- Noel Caplice, PhD
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Alatutkija:
- Florence Herrison, PhD
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Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
Inclusion Criteria:
- Be able to give written informed consent.
- Males & females aged 18 to 70 years (inclusive).
- Has a BMI between ≥30 and ≤40 kg/m2.
- HbA1c between ≥38.8 and ≤47 mmol/mol (5.7-6.4 %)
- Has a stable body weight (≤5 % change) over the past 3-months.
- Is in general good health, as determined by the investigator.
- Willing to consume the investigational product daily for the duration of the trial.
- Willing to wear a continuous glucose monitoring sensor for two 14-day periods.
- Be willing to maintain stable dietary habits and physical activity levels throughout the trial period.
Exclusion Criteria:
1. Are aged less than 18 or greater than 70 years. 2. Participants who are pregnant, breastfeeding, or wish to become pregnant during the trial.
3. Participants currently of childbearing potential, but not using an effective method of contraception, as outlined below:
- Complete abstinence from intercourse two weeks prior to administration of the investigational product, throughout the clinical trial, until the completion of follow-up procedures or for two weeks following discontinuation of the investigational product in cases where participant discontinues the trial prematurely. (Participants utilising this method must agree to use an alternate method of contraception if they should become sexually active and will be queried on whether they have been abstinent in the preceding 2 weeks when they present to the clinic for the Final Visit).
- Has a male sexual partner who is surgically sterilised prior to the Screening Visit and is the only male sexual partner for that participant.
- Sexual partner(s) is/are exclusively female.
- Use of acceptable method of contraception, such as a spermicide, mechanical barrier (e.g., male condom, female diaphragm) or contraceptive pill. The participant must be using this method for at least 1 week following the end of the trial.
Use of any non-hormonal intrauterine device (IUD) or contraceptive implant with published data showing that the highest expected failure rate is less than 1 % per year. The participant must have the device inserted at least 2 weeks prior to the first Screening Visit, throughout the trial, and 2 weeks following the end of the trial.
4. Are hypersensitive to any of the components of the investigational product or common food allergens.
5. Has taken antibiotics within the previous 12-weeks prior to randomisation 6. Participant regularly takes probiotics, prebiotics, or fibre supplements (daily use in the 4 weeks prior to screening and up to baseline) 7. Has an intake of more than 19 g of fibre per day. 8. Has taken anti-obesity medication/supplement within the previous 12-weeks prior to randomisation.
9. Participant is actively or has recently (3 months prior to randomisation) participated in a weight loss program or weight change of 5 % during the past 3 months.
10. Participant has Type 1 or Type 2 Diabetes Mellitus. 11. Has a history of bariatric surgery. 12. Participant who is severely immuno-compromised (HIV positive, transplant patient, on antirejection medications, or has undergone chemotherapy or radiotherapy within the last year).
13. Participant has significant comorbidities or an uncontrolled disease, as determined by the PI/Sub-Investigator on the basis of medical history and routine laboratory test results that may adversely affect the participant's ability to complete the trial or it's assessments or which may pose significant risk to the participant.
14. Participant has a history of co-existing gastrointestinal, and/or gynaecological, and/or urologic pathology (e.g., colon cancer, colitis, Crohn's Disease, Celiac, Endometriosis, prostate cancer) or lactose intolerance.
15. Has a gastrointestinal or chronic infective disease (i.e., diarrhoea, Crohn's disease, ulcerative colitis, irritable bowel syndrome, diverticulosis, stomach or duodenal ulcers, hepatitis, HIV, cancer, etc.), or with a history of such diseases.
16. Has a history of drug and/or alcohol abuse at the time of enrolment.
- Consumes greater than nationally recommended units of alcohol per week (>11 units for women & >17 units for men).
- Is currently in treatment (or has been in the last 6 months) for alcohol/substance abuse
Has been diagnosed with alcohol/substance abuse disorder. 17. Has used oral/injectable steroids within the previous 30 days prior to Screening (or between Screening/Baseline Visit).
18. Taking a medication that the investigator believes would interfere with the objectives of the trial or pose a safety risk or confound the interpretation of the trial results. Prohibited medications include:
- Metformin
Anti-psychotic drugs 19. If taking anti-hypertensive drugs, anti-depressive drugs, statins, or any other medication that the investigator determines could impact the results of the study, the participant must have been taking the product for at least 3 months prior to screening. (Changes to the dose during the trial will be assessed by the investigator for impact on trial results).
20. Individual who work a shift work pattern that requires them to work >1 nightshift per week.
21. Individuals living in the same residence as a previously or currently enrolled participants on the trial.
22. Individuals who, in the opinion of the investigator, are considered to be poor attendees or unlikely for any reason to be able to comply with the trial.
23. Participant is currently, or planning, to participate in another interventional study during the study period.
24. Participants may not be receiving treatment involving experimental drugs. If the participant has been in a recent experimental trial, these must have been completed not less than 30 days prior to this trial.
25. Individuals who have a history of non-compliance or, in the opinion of the investigator, are considered to be poor attendees or unlikely for any reason to be able to comply with the trial.
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Perustiede
- Jako: Satunnaistettu
- Inventiomalli: Rinnakkaistehtävä
- Naamiointi: Kolminkertaistaa
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
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Kokeellinen: Soluble Corn Fibre
12g compound per Sachet (providing 10g fibre) consumed twice per day
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10g soluble corn fibre to be consumed twice per day
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Placebo Comparator: Maltodextrin
Calorie matched control of 2 g compound per sachet (0 g fibre), composed of: Maltodextrin, consumed twice per day
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2g maltodextrin consumed twice per day
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Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Change in plasma HbA1c concentration
Aikaikkuna: 16 weeks
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Change from baseline to week 16 in the treatment group compared to placebo on plasma HbA1c (mmol/mol) concentration
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16 weeks
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Toissijaiset tulostoimenpiteet
Tulosmittaus |
Aikaikkuna |
|---|---|
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Change in post-prandial Blood Glucose (mmol/L) measured by incremental Area Under the Curve (iAUC) derived from an Oral Glucose Tolerance Test (OGTT)
Aikaikkuna: 16 weeks
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16 weeks
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Change in post-prandial Blood Glucose maximal concentration, derived from an Oral Glucose Tolerance Test (OGTT)
Aikaikkuna: 16 weeks
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16 weeks
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Change in post-prandial Blood Glucose time to peak, derived from an Oral Glucose Tolerance Test (OGTT)
Aikaikkuna: 16 weeks
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16 weeks
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Change in post-prandial insulin (mIU/L) as measured by incremental Area Under the Curve (iAUC) derived from an Oral Glucose Tolerance Test (OGTT)
Aikaikkuna: 16 weeks
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16 weeks
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Change in post-prandial insulin maximal concentration (Cmax) derived from an Oral Glucose Tolerance Test (OGTT)
Aikaikkuna: 16 weeks
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16 weeks
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Change in post-prandial Blood Insulin time to peak (Tmax), derived from an Oral Glucose Tolerance Test (OGTT)
Aikaikkuna: 16 weeks
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16 weeks
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Change in insulin resistance (mIU/L)
Aikaikkuna: 16 weeks
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16 weeks
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Change in lipids (mmol/L): Triglycerides (TG), Total Cholesterol (TC), High-Density Lipoprotein Cholesterol (HDL), Low-Density Lipoprotein Cholesterol (LDL)
Aikaikkuna: 16 weeks
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16 weeks
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Change in waist-to-hip ratio
Aikaikkuna: 16 weeks
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16 weeks
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Change in BMI (kg/m2)
Aikaikkuna: 16 weeks
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16 weeks
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Continuous blood glucose monitoring (during run-in & 2-weeks before End of Study) as measured by Freestyle Libre Glucose Monitoring System, a continuous glucose monitoring (CGM) device.
Aikaikkuna: 16 weeks
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16 weeks
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Change in Fasting Blood Glucose (FBG) (mmol/L)
Aikaikkuna: 16 weeks
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16 weeks
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Change in Fasting Insulin (mIU/L).
Aikaikkuna: 16 weeks
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16 weeks
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Muut tulostoimenpiteet
Tulosmittaus |
Aikaikkuna |
|---|---|
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Change in gut hormones (GLP-1 and PYY) measured by iAUC (T-15 to T120 minutes)
Aikaikkuna: 16 weeks
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16 weeks
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Change in self-reported hunger and satiety measured by iAUC (T-15 to T120 minutes)
Aikaikkuna: 16 weeks
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16 weeks
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Change in the composite score of gastrointestinal symptoms, (bloating score + abdominal cramping score + stomach noises score + flatulence score)
Aikaikkuna: 16 weeks
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16 weeks
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Change in stool consistency (Bristol Stool Scale) and frequency
Aikaikkuna: 16 weeks
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16 weeks
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Change in Faecal Short Chain Fatty Acids (fSCFA) microbiota
Aikaikkuna: 16 weeks
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16 weeks
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Change in TNF alpha
Aikaikkuna: 16 weeks
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16 weeks
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Yhteistyökumppanit ja tutkijat
Sponsori
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Todellinen)
Ensisijainen valmistuminen (Odotettu)
Opintojen valmistuminen (Odotettu)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Avainsanat
Muita asiaankuuluvia MeSH-ehtoja
Muut tutkimustunnusnumerot
- AFCRO-129
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