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:
2025-12-24 @ 10:55 PM
Ignite Modification Date:
2025-12-24 @ 10:55 PM
NCT ID:
NCT01540669
Eligibility Criteria:
Inclusion Criteria:
* Age between 18 and 70 years
* Body mass index between 18.5 and 29.9 kg/m2 (encompasses normal weight and overweight)
* Meets the Rome III criteria for functional constipation as follows: (Criteria fulfilled for the last 3 months with symptom onset at least 6 months prior to diagnosis):
Must meet 2 or more of the following criteria:
* Straining during at least 25% of defecations
* Lumpy or hard stools in at least 25% of defecations
* Sensation of incomplete evacuation for at least 25% of defecations
* Sensation of anorectal obstruction/blockage for at least 25% of defecations
* Manual maneuvers to facilitate at least 25% of defecations (e.g., digital evacuation, support of the pelvic floor)
* Fewer than three defecations per week
* Loose stools are rarely present without the use of laxatives
* Insufficient criteria for irritable bowel syndrome
* Ability of the participant (in the investigator's opinion) to comprehend the full nature and purpose of the study including possible risks and side effects
* Consent to the study and willing to comply with study product and methods
* Willingness to maintain a stable diet throughout the study
* Consistent use and dose of chronic medication, if any, in the past 30 days
Exclusion Criteria:
* Major gastrointestinal complication (e.g. Crohn"s disease, colitis, celiac disease)
* Febrile diverticulitis within 1 year of screening
* Pelvic floor dysfunction
* Prior abdominal surgery that in the opinion of the investigator may present a risk for the subject or confound study results
* Prior abdominal surgery of the following type: gastric bypass, lap band, colectomy, removal of gall bladder
* Clinically significant underlying systemic illness that may preclude the subject"s ability to complete the trial or that may confound the study outcomes
* Any clinically relevant abnormalities in the physical examination or in laboratory variables before entry into the study
* Daily consumption of probiotics, prebiotics, fermented milk, and/or yogurt within 2 weeks of screening
* Laxative, fiber supplement, or other constipation medication (e.g. prokinetic drugs) use within 2 weeks of screening
* Antibiotic use within 1 month of enrollment
* Regular use of any drug or dietary supplement known to cause constipation (e.g. iron, opioids, sucralfate, misoprostol, 5-HT#- antagonists, antacids with magnesium or aluminum, or diarrhea medication)
* Anticipated major dietary or exercise changes during the study period
* Known allergies to any substance in the study product
* Pregnant or lactating female, or pregnancy planned during study period
* Eating disorder
* History of alcohol, drug, or medication abuse
* Participation in another study with any investigational product within 3 months of screening
* Investigator believes that the participant may be uncooperative and/or noncompliant and should therefore not participate in the study
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
70 Years
Study:
NCT01540669
Study Brief:
Protocol Section:
NCT01540669