Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 12:32 AM
Ignite Modification Date:
2025-12-25 @ 12:32 AM
NCT ID:
NCT02784067
Eligibility Criteria:
Inclusion Criteria:
1. Subject is 16 years of age or older.
2. Subject is male or female. Women of childbearing potential must be willing to use one of the following contraception methods (for at least 10 days prior to start of study drug and for 10 to 14 days after last dose of study drug): Oral contraceptive, Injectable progestogen, Implants of levonorgestrel, Estrogenic vaginal ring, Percutaneous contraceptive patches, Intrauterine device, Sterile male partner, Double-barrier method of contraception Women of non-child bearing potential include females regardless of age with functioning ovaries and who have a current tubal ligation (Hatcher, 2004), bilateral oophorectomy, or total hysterectomy, or post-menopausal females. Note: Post-menopausal is defined as 1 year without menses with an appropriate clinical profile (e.g., age appropriate, \>45 years, in the absence of hormone replacement therapy).
3. Subject has a minimum of 3 months of self-reported diarrhea (BSFS scores ≥ 5 on at least 3 days per week and ≥1 stool per day)
4. Subject has a value in the SHMBT of at least 20 ppm for hydrogen, or 12 ppm for methane or 15 ppm above a previous breath sample for the combination of both gases.
5. Subject reports that he/she experienced soft stools or diarrhea within the last 24 hours when contacted by the site 24 hours after completing the SHMBT.
6. Subject is able to read, speak, and verbally understand the English language.
7. Subject is located in the United States.
8. Subject has access to the Internet on a daily basis.
9. Subject has access to an acceptable Apple iPhone/iPad/iTouch or Android smartphone/tablet. The sponsor may choose to provide a smartphone in unusual cases (please contact sponsor to request loaner device when applicable)
Exclusion Criteria:
1. Subject has recent history of functional or chronic constipation.
2. Subject has known history of ulcerative colitis, Crohn's disease, or Celiac disease.
3. Subject has known hypersensitivity to papain, glycerol, or yeast.
4. Subject has received bovine serum in the last year.
5. Subject has previous history of Sucraid use.
6. Subject has taken any prebiotic or probiotic within 5 days prior to Visit 2 and does not agree to refrain from taking them during the study.
7. Subject is female and is pregnant, breastfeeding, or planning to become pregnant during the study.
8. Subject has known uncontrolled systemic disease.
9. Subject has prior diagnosis of Type 1 or Type 2 diabetes.
10. Subject has history of bowel resection.
11. Subject is undergoing chemotherapy for the treatment of cancer.
12. Subject has major physical or psychiatric illness within the last 6 months that in the opinion of the investigator would affect the subject's ability to complete the trial.
13. Subject has used an investigational device or investigational drug within 30 days prior to Visit 1.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
16 Years
Study:
NCT02784067
Study Brief:
Protocol Section:
NCT02784067