- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT07703254
A Clinical Trial to Investigate the Efficacy of Acacia Fiber on Gastrointestinal Health and Microbiota Composition in Healthy Adults With Occasional Constipation
A Randomized, Triple-Blind, Placebo Controlled, Parallel Clinical Trial to Investigate the Efficacy of Acacia Fiber on Gastrointestinal Health and Microbiota Composition in Healthy Adults With Occasional Constipation
The goal of this randomized blinded placebo-controlled clinical trial is to investigate the effect of low- and high-dose supplementation of Acacia fiber on gut health and microbiota composition in adults with occasional constipation in a controlled diet context. Acacia fiber is a soluble dietary fiber with prebiotic properties, and this study evaluates its role in modulating gut microbiota and associated gastrointestinal outcomes. Acacia fiber has previously demonstrated improvements in stool frequency in the context of an irritable bowel syndrome with constipation (IBS-C)-characterized population. The main questions this study aims to answer are: Does Acacia fiber supplementation (5 g or 10 g) improve the frequency of bowel movements or stool consistency (assessed by Bristol Stool Scale) in the context of healthy population with occasional constipation? Does Acacia fiber benefit on gut health correlates with specific gut microbiota modulation characterised by shotgun sequencing? What are mechanistical faecal & blood markers that may support this correlation? Researchers will compare low-dose Acacia fiber (5 g), high-dose Acacia fiber (10 g), and placebo to see if Acacia fiber modulates gut microbiota composition in a manner consistent with prebiotic activity and whether these changes are associated with improvements in bowel movement frequency and stool consistency. Participants will:
- Take a daily supplement of either 5 g Acacia fiber, 10 g Acacia fiber, or placebo
- Complete study diaries, including the Bowel Habits Diary and Bristol Stool Scale
- Complete the Patient Assessment of Constipation Quality of Life, modified Gastrointestinal Symptoms Rating Scale, and sleep and stress Likert scales
- Complete 3-day food records
Přehled studie
Postavení
Typ studie
Zápis (Odhadovaný)
Fáze
- Nelze použít
Kontakty a umístění
Studijní kontakt
- Jméno: Erin Lewis, PhD
- Telefonní číslo: 248 1-226-242-4551
- E-mail: elewis@kgkscience.com
Studijní záloha kontaktů
- Jméno: Damien Guillemet
- Telefonní číslo: +33 2 32 83 18 18
- E-mail: d.guillemet@nexira.com
Studijní místa
-
-
Ontario
-
London, Ontario, Kanada, N5Y 5V6
- KGK Science Inc.
-
-
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
Přijímá zdravé dobrovolníky
Popis
Inclusion Criteria:
- Males and females aged between 30 and 60 years old, inclusive
- Body Mass Index (BMI) between 18.5 to 29.9 kg/m², inclusive
- Stable body weight defined as a <5% change in body weight in the three months prior to baseline as assessed by the Qualified Investigator (QI)
Participants must meet the following criteria of occasional constipation for the past 3 months. This will be assessed at screening and confirmed over a 2-week period prior to baseline:
- 5 CSBMs per week AND either one of the following: at least 25% of Bowel Movements (BMs) are BSS type 1 or 2 OR straining for most of the BMs (≥50%), defined as 3 minutes or more during BM, as assessed by the QI
OR,
At least 50% of BMs are BSS type 1 and 2, as assessed by the QI
OR,
≤ 3 CSBMs per week as assessed by the QI
- Low to moderate fiber intake, defined as < 18 g per day for women and < 22 g per day for men, as assessed by the Food Frequency Questionnaire (FFQ)
- Females not of child-bearing potential, defined as those who have undergone a sterilization procedure (e.g. hysterectomy, bilateral oophorectomy, bilateral tubal ligation, complete endometrial ablation) or have been post-menopausal for at least 1 year prior to screening
OR,
Individuals of child-bearing potential must have a negative baseline urine pregnancy test and agree to use a medically approved method of birth control for the duration of the study. All hormonal birth control must have been in use for a minimum of three months. Acceptable methods of birth control include:
Hormonal contraceptives including oral contraceptives, hormone birth control patch (Ortho Evra), vaginal contraceptive ring (NuvaRing), injectable contraceptives (Depo-Provera, Lunelle), or hormone implant (Norplant System)
Double-barrier method
Intrauterine devices
Non-heterosexual lifestyle and agrees to use contraception if planning on changing to heterosexual partner(s)
Vasectomy of partner at least 6 months prior to screening
Abstinence and agrees to use contraception if planning on becoming sexually active during the study
- Agrees to maintain current lifestyle habits (diet, sleep, physical activity, medications, supplements, and without any new addition) as much as possible throughout the study
- Provided voluntary, written, informed consent to participate in the study
- Healthy as determined by medical history and laboratory results as assessed by the Qualified Investigator (QI)
- Willing and able to comply with the study protocol (e.g., concomitant treatment) and complete questionnaires, records and diaries associated with the study, as well as complete all clinic visits
Exclusion Criteria:
- Individuals who are pregnant, breast feeding, or planning to become pregnant during the study
- Allergy, sensitivity or intolerance, to study products
- Chronic constipation, as assessed by the QI
- Following a specific diet (e.g., vegetarian, paleo, ketogenic, carnivore)
- Colonoscopy within four weeks prior to baseline or during the study
- Gastrointestinal related sensitivities including gluten and lactose intolerance
- Current or history of any significant diseases of the gastrointestinal tract (e.g., irritable bowel syndrome, irritable bowel disease, gastrointestinal surgery) as assessed by the QI
- Unstable metabolic disease, autoimmune disease or chronic diseases as assessed by the QI
- Unstable hypertension. Treatment on a stable dose of medication for at least 3 months will be considered by the QI (See Section 8.3.1)
- Type I diabetes
- Type II diabetes if on insulin treatment. Type II diabetics on stable medication for at least three months and an Hemoglobin A1c (HbA1c) of <8.0% may be included after assessment by the QI on a case-by-case basis
- Significant cardiovascular event in the past 6 months. Participants with no significant cardiovascular event on stable medication may be included after assessment by the QI on a case-by-case basis
- History of or current diagnosis with kidney and/or liver diseases as assessed by the QI on a case-by-case basis, with the exception of history of kidney stones in participants who are symptom free for 6 months
- Self-reported confirmation of current or pre-existing thyroid condition. Treatment on a stable dose of medication for at least 3 months will be considered by the QI
- Major surgery in the past 3 months or individuals who have planned surgery during the course of the study. Participants with minor surgery will be considered on a case-by-case basis by the QI
- Cancer, except skin basal cell carcinoma completely excised with no chemotherapy or radiation with a follow up that is negative. Volunteers with cancer in full remission for more than five years after diagnosis are acceptable
- Individuals with an autoimmune disease or are immune compromised as assessed by the QI
- Self-reported confirmation of a Human Immunodeficiency Virus (HIV)-, Hepatitis B- and/or C-positive diagnosis as assessed by the QI
- Self-reported confirmation of blood/bleeding disorders as assessed by the QI
- Use of prescribed cannabinoid products
- Chronic use of cannabinoid products (>2 times/week). Occasional users will be required to washout for at least 60 days and abstain for the duration of the study period
- Regular use of tobacco or nicotine products within the past three years, as assessed by the QI.
- Alcohol intake average of >2 per day or >10 per week of standard drinks as assessed by the QI
- Alcohol or drug abuse within the last 12 months
- Current use of prescribed and/or over-the-counter (OTC) medications, supplements, and/or consumption of food/drinks that may impact the efficacy and/or safety of the investigational product, gut transit and/or constipation, or gut microbiota characteristics (e.g., fibre, pre- pro- postbiotic, polyphenols extract, etc.) (Section 8.3)
- Clinically significant abnormal laboratory results at screening as assessed by the QI
- Blood donation 30 days prior to baseline, during the study, or a planned donation within 30 days of the last study visit
- Participation in other clinical research studies 60 days prior to baseline, as assessed by the QI
- Individuals who are unable to give informed consent
- Any other condition or lifestyle factor, that, in the opinion of the QI, may adversely affect the participant's ability to complete the study or its measures or pose significant risk to the participant
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Randomizované
- Intervenční model: Paralelní přiřazení
- Maskování: Čtyřnásobek
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Komparátor placeba: Placebo
|
Starting the day following the baseline visit (Day 1), participants will take 1 sachet daily for 4 days, then increase to 2 sachets daily until the day prior to the end-of-study visit (Day 56).
Each sachet will be mixed with a usual food or beverage prior to consumption.
|
|
Experimentální: Low-dose Acacia fiber
|
Starting the day following the baseline visit (Day 1), participants will take 1 sachet daily for 4 days, then increase to 2 sachets daily until the day prior to the end-of-study visit (Day 56).
Each sachet will be mixed with a usual food or beverage prior to consumption.
|
|
Experimentální: High-dose Acacia fiber
|
Starting the day following the baseline visit (Day 1), participants will take 1 sachet daily for 4 days, then increase to 2 sachets daily until the day prior to the end-of-study visit (Day 56).
Each sachet will be mixed with a usual food or beverage prior to consumption.
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Frequency of complete and spontaneous bowel movements
Časové okno: Baseline to Day 56
|
Frequency of complete and spontaneous bowel movements (CSBMs), as assessed by the Bowel Habits Diary (BHD)
|
Baseline to Day 56
|
|
Stool consistency
Časové okno: Baseline to Day 56
|
Stool consistency, as assessed by the Bristol Stool Scale (BSS).
The BSS is a 7-item stool description and image scale that assesses the shape and consistency of stool.
Scores range from 1 to 7, with higher scores indicating looser stool consistency and lower scores indicating harder stool consistency.
|
Baseline to Day 56
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Gut Microbiota Composition
Časové okno: Baseline to Day 56
|
Change from baseline to Day 56 between Acacia fiber (5g or 10g) and placebo in gut microbiota composition, as assessed by fecal microbiome shotgun sequencing
|
Baseline to Day 56
|
|
Frequency of CSBMs
Časové okno: Baseline to Day 28
|
Change from baseline to Day 28 between Acacia fiber (5g or 10g) and placebo in frequency of CSBMs, as assessed by the BHD
|
Baseline to Day 28
|
|
Stool Consistency
Časové okno: Baseline to Day 28
|
Change from baseline to Day 28 between Acacia fiber (5g or 10g) and placebo in stool consistency, as assessed by the Bristol Stool Scale (BSS).
The BSS is a 7-item stool description and image scale that assesses the shape and consistency of stool.
Scores range from 1 to 7, with higher scores indicating looser stool consistency and lower scores indicating harder stool consistency.
|
Baseline to Day 28
|
|
Digestive symptoms
Časové okno: Baseline to Day 28 and Day 56
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in digestive symptoms as assessed by Gastrointestinal Symptom Rating Scale (GSRS).
The modified GSRS consists of 14 items on a four-point scale (0-3).
It assesses abdominal pain, reflux syndrome, diarrhea syndrome, indigestion syndrome, and constipation syndrome.
Higher scores indicate more severe gastrointestinal symptoms.
|
Baseline to Day 28 and Day 56
|
|
Patient Assessment of Constipation Quality of Life questionnaire (PAC-QoL)
Časové okno: Baseline to Day 28 and Day 56
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in Quality of life as assessed by Patient Assessment of Constipation Quality of Life questionnaire (PAC-QoL).
The PAC-QoL consists of 28-items with four subscales (worries and concerns, physical discomfort, psychosocial discomfort, and satisfaction), and an overall scale.
Items are scored on a 5-point Likert scale ranging from 0 to 4, with lower scores indicating better constipation-related quality of life.
|
Baseline to Day 28 and Day 56
|
|
Proportion of CSBMs with complete defecation
Časové okno: Day 28 and Day 56
|
The difference in the proportion of CSBMs with complete defecation at Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo
|
Day 28 and Day 56
|
|
proportion of participants with occasional constipation
Časové okno: Day 56
|
The difference in the proportion of participants with occasional constipation at Day 56 between Acacia fiber (5g or 10g) and placebo
|
Day 56
|
|
Sleep and Stress
Časové okno: Baseline to Day 28 and Day 56
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in sleep and stress, as assessed by the sleep and stress Likert scales.
Four-point Likert scales will be used to measure the participant's perceived sleep quality (strongly disagree - 0, disagree - 1, agree - 2, strongly agree - 3) and stress (no stress - 0, minimally stressed - 1, moderately stressed - 2, extremely stressed - 3).
Participants will be instructed to indicate their response on the scale for the following statements: "Overall, I am satisfied with my sleep" and " Rate your current stress level".
Higher scores indicate greater perceived stress.
|
Baseline to Day 28 and Day 56
|
Další výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Change from baseline to Day 28 between Acacia fiber (5g or 10g) and placebo in gut microbiota composition, as assessed by fecal microbiome shotgun sequencing
Časové okno: Baseline to Day 28
|
Change from baseline to Day 28 between Acacia fiber (5g or 10g) and placebo in gut microbiota composition, as assessed by fecal microbiome shotgun sequencing
|
Baseline to Day 28
|
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in short-chain fatty acids (SCFAs)
Časové okno: Baseline to Day 28 and Day 56
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in constipation related fecal biomarkers (short-chain fatty acids (SCFAs).
|
Baseline to Day 28 and Day 56
|
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in lipopolysaccharides (LPS) and LPS binding proteins
Časové okno: Baseline to Day 28 and Day 56
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in constipation related fecal biomarkers (lipopolysaccharides (LPS) and LPS binding proteins).
|
Baseline to Day 28 and Day 56
|
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in primary and secondary bile acids
Časové okno: Baseline to Day 28 and Day 56
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in constipation related fecal biomarkers (primary and secondary bile acids).
|
Baseline to Day 28 and Day 56
|
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in fecal serotonin
Časové okno: Baseline to Day 28 and Day 56
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in constipation related fecal biomarkers (serotonin).
|
Baseline to Day 28 and Day 56
|
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in Immunoglobulin A
Časové okno: Baseline to Day 28 and Day 56
|
Change from baseline to Day 28 and Day 56 between Acacia fiber (5g or 10g) and placebo in constipation related fecal biomarkers (Immunoglobulin A).
|
Baseline to Day 28 and Day 56
|
|
Change from baseline to Day 56 between Acacia fiber (5g or 10g) and placebo in plasma short-chain fatty acid (SCFA) concentrations
Časové okno: Baseline to Day 56
|
Change from baseline to Day 56 between Acacia fiber (5g or 10g) and placebo in constipation related blood biomarkers (SCFAs)
|
Baseline to Day 56
|
|
Change from baseline to Day 56 between Acacia fiber (5g or 10g) and placebo in plasma lipopolysaccharide (LPS) concentrations
Časové okno: Baseline to Day 56
|
Change from baseline to Day 56 between Acacia fiber (5g or 10g) and placebo in constipation related blood biomarkers (LPS)
|
Baseline to Day 56
|
|
Change from baseline to Day 56 between Acacia fiber (5g or 10g) and placebo in plasma zonulin
Časové okno: Baseline to Day 56
|
Change from baseline to Day 56 between Acacia fiber (5g or 10g) and placebo in constipation related blood biomarkers (zonulin)
|
Baseline to Day 56
|
|
Change from baseline to Day 56 between Acacia fiber (5g or 10g) and placebo in plasma serotonin
Časové okno: Baseline to Day 56
|
Change from baseline to Day 56 between Acacia fiber (5g or 10g) and placebo in constipation related blood biomarkers (serotonin)
|
Baseline to Day 56
|
|
Change from baseline to Day 56 between Acacia fiber (5g or 10g) and placebo in plasma motilin
Časové okno: Baseline to Day 56
|
Change from baseline to Day 56 between Acacia fiber (5g or 10g) and placebo in constipation related blood biomarkers (motilin)
|
Baseline to Day 56
|
|
Incidence of post-emergent adverse events (AE)
Časové okno: From screening (Day -45 to Day -15) through final study visit (Visit 4)
|
Incidence of post-emergent adverse events (AE)
|
From screening (Day -45 to Day -15) through final study visit (Visit 4)
|
|
Clinically relevant changes in blood pressure after supplementation
Časové okno: From screening (day -45 to day -15) through final study visit (visit 4)
|
Changes in blood pressure (mmHg) after supplementation
|
From screening (day -45 to day -15) through final study visit (visit 4)
|
|
Change in complete blood count following supplementation
Časové okno: At screening (day -45 to day -15) and visit 4 (day 56)
|
Clinically relevant changes in complete blood count after supplementation
|
At screening (day -45 to day -15) and visit 4 (day 56)
|
|
Change in plasma aspartate aminotransferase (AST) concentration following supplementation
Časové okno: At screening (day -45 to day -15) and visit 4 (day 56)
|
Clinically relevant changes in clinical chemistry (aspartate aminotransferase (AST)) after supplementation
|
At screening (day -45 to day -15) and visit 4 (day 56)
|
|
Change in plasma alanine aminotransferase (ALT) concentration following supplementation
Časové okno: At screening (day -45 to day -15) and visit 4 (day 56)
|
Clinically relevant changes in clinical chemistry (alanine aminotransferase (ALT)) after supplementation
|
At screening (day -45 to day -15) and visit 4 (day 56)
|
|
Change in plasma alkaline phosphatase (ALP) concentration following supplementation
Časové okno: At screening (day -45 to day -15) and visit 4 (day 56)
|
Clinically relevant changes in clinical chemistry (alkaline phosphatase (ALP)) after supplementation
|
At screening (day -45 to day -15) and visit 4 (day 56)
|
|
Change in total bilirubin following supplementation
Časové okno: At screening (day -45 to day -15) and visit 4 (day 56)
|
Clinically relevant changes in total bilirubin after supplementation
|
At screening (day -45 to day -15) and visit 4 (day 56)
|
|
Change in creatinine following supplementation
Časové okno: At screening (day -45 to day -15) and visit 4 (day 56)
|
Clinically relevant changes in creatinine after supplementation
|
At screening (day -45 to day -15) and visit 4 (day 56)
|
|
Change in estimated glomerular filtration rate (eGFR) following supplementation
Časové okno: At screening (day -45 to day -15) and visit 4 (day 56)
|
Clinically relevant changes in estimated glomerular filtration rate (eGFR) after supplementation
|
At screening (day -45 to day -15) and visit 4 (day 56)
|
|
Change in potassium following supplementation
Časové okno: At screening (day -45 to day -15) and visit 4 (day 56)
|
Clinically relevant changes in serum potassium after supplementation
|
At screening (day -45 to day -15) and visit 4 (day 56)
|
|
Change in sodium following supplementation
Časové okno: At screening (day -45 to day -15) and visit 4 (day 56)
|
Clinically relevant changes in serum sodium after supplementation
|
At screening (day -45 to day -15) and visit 4 (day 56)
|
|
Change in chloride following supplementation
Časové okno: At screening (day -45 to day -15) and visit 4 (day 56)
|
Clinically relevant changes in serum chloride after supplementation
|
At screening (day -45 to day -15) and visit 4 (day 56)
|
|
Clinically relevant changes in heart rate after supplementation
Časové okno: From screening (day -45 to day -15) through final study visit (visit 4)
|
Changes in heart rate (beats per minute) after supplementation
|
From screening (day -45 to day -15) through final study visit (visit 4)
|
Spolupracovníci a vyšetřovatelé
Sponzor
Spolupracovníci
Vyšetřovatelé
- Vrchní vyšetřovatel: David Crowley, MD, KGK Science Inc.
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Odhadovaný)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další identifikační čísla studie
- FIB16 / 25NXCRR01
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .
Klinické studie na Gastrointestinální zdraví
-
Biostime Institute of Nutrition and CareDokončeno
-
University of ZurichDokončenoOutcome Assessment, Health CareŠvýcarsko
-
University of BernUniversity Hospital Inselspital, BerneDokončenoNeuroscience of Dreaming, HealthŠvýcarsko
-
Onconic Therapeutics Inc.DokončenoDrogové interakce a bezpečnost mezi JP-1366, amoxicilinem a klarithromycinem u zdravých dobrovolníkůHelicobacter Pylori Associated Gastrointestinal DiseaseKorejská republika
-
University of Colorado, DenverEunice Kennedy Shriver National Institute of Child Health and Human Development... a další spolupracovníciDokončenoPreventivní zdravotní služby (PREV HEALTH SERV)Spojené státy
-
Queens College, The City University of New YorkNáborZveřejnění článků předložených American Journal of Public HealthSpojené státy
-
Seattle Children's HospitalEunice Kennedy Shriver National Institute of Child Health and Human Development... a další spolupracovníciZatím nenabírámePreventivní zdravotní služby (PREV HEALTH SERV)Spojené státy
-
University of WashingtonNational Institute of Environmental Health Sciences (NIEHS)Aktivní, ne náborTeplo | Havarijní připravenost | Extrémní teplo | Health Health | Extrémní tepelné vlny | Řízení katastrof | Plánování katastrof | KatastrofySpojené státy
-
Assiut UniversityZatím nenabírámeGIT - Gastrointestinal Tract Hemorrhage
-
Kliniek ViaSanaSt. Anna Ziekenhuis, Geldrop, NetherlandsDokončenoBolest | Užívání opioidů | Totální náhrada kolena | Aplikace E-healthHolandsko