Study to Evaluate the Tolerability of Prebiotics on the Microbiota

Healthy Clinical Trial

Official title:

A Randomised, Single-Blind, Controlled Study to Evaluate the Tolerability of Prebiotics on the Microbiota

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02628652
• Other study ID #: AFCRO-057
• Status: Completed
• Phase: N/A
• First received: December 2, 2015
• Last updated: February 22, 2016
• Start date: October 2015
• Est. completion date: December 2015

Study information

• Verified date: February 2016
• Source: Kaleido Biosciences
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The primary objective of this study is to determine the tolerability of two polyglycan food ingredients, GOS and GLOS, at two different levels in healthy human subjects. The comparator in this study will be Inulin FOS, a commercially available glycan supplement.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 45
• Est. completion date: December 2015
• Est. primary completion date: December 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

1. Be able to give written informed consent,

2. Be male or female, between 18 and 40 years of age,

3. Have a BMI = 20 & = 27 kg/m2,

4. Be a non-pregnant female,

5. Be in generally good health,

6. Subjects will continue on his/her normal diet and exercise routine,

7. Be an Irish National.

Exclusion Criteria:

1. Are less than 18 and greater than 40 years of age,

2. Females are pregnant, lactating or wish to become pregnant during the study. Female subject is currently either of:

• non-childbearing potential (i.e., physiologically incapable of becoming pregnant, including any female who is post-menopausal or any female who is surgically sterilized (via documented hysterectomy or bilateral tubal ligation). (For purposes of this study, postmenopausal is defined as one year without menses), OR

• child bearing potential, the subject is eligible to enter and participate in this study if she is not lactating and has a negative urine pregnancy test at the screening visit, visit 2 and upon completion of the study at visit 7. The subject must also agree to one of the following methods of contraception: i. Complete abstinence from intercourse two weeks prior to administration of study, throughout the clinical trial, until the completion of follow-up procedures or for two weeks following discontinuation of the study medication in cases where subject discontinues the study prematurely. (Subjects utilizing 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.) or, ii. has a male sexual partner who is surgically sterilized prior to the Screen Visit and is the only male sexual partner for that subject or, iii. sexual partner(s) is of the same gender or, iv. Oral or implant contraceptives (either combined or progestogen only) with double-barrier method of contraception consisting of spermicide with either condom or diaphragm. (Women of child-bearing potential using an oral contraceptive in combination with a double-barrier method of contraception are required to continue to use this form of contraception for 1 week following discontinuation of study medication) or, v. Use of double-barrier contraception, specifically, a spermicide plus a mechanical barrier (e.g. male condom, female diaphragm). The subject must be using this method for at least 1 week following the end of the study or, vi. Use of any intrauterine device (IUD) with published data showing that the highest expected failure rate is less than 1% per year. The subject must have the device inserted at least 2 weeks prior to the first Screen Visit, throughout the study, and 2 weeks following the end of the study.

3. Are hypersensitive to any of the components of the test product,

4. Are currently taking probiotic or prebiotic supplements, or have taken them in the past 28 days,

5. Unwilling to avoid probiotics/prebiotics supplements for the duration of the study

6. Subject has taken antibiotics in the previous 3 months,

7. Have a significant acute or chronic, unstable and untreated disease or any condition which contraindicates, in the investigators judgement, entry to the study,

8. Subject is a smoker,

9. Subject has a history of drug and/or alcohol abuse at the time of enrolment,

10. Having a condition or have taken a medication that the investigator believes would interfere with the objectives of the study, pose a safety risk or confound the interpretation of the study results;

11. 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,

12. Subjects may not be receiving treatment involving experimental drugs,

13. If the subject has been in a recent experimental trial, these must have been completed not less than 60 days prior to this study,

14. Have a malignant disease or any concomitant end-stage organ disease.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject)

Related Conditions & MeSH terms

• Healthy

Intervention

Dietary Supplement:
• GOS

• GLOS

• FOS

Locations

Country	Name	City	State
Ireland	Atlantia Food Clinical Trials/ University Cork College	Cork

Sponsors (1)

Lead Sponsor	Collaborator
Kaleido Biosciences

Country where clinical trial is conducted

Ireland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of subjects with Adverse Events in each group		28 Days	Yes