Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-25 @ 1:07 AM
Ignite Modification Date:
2025-12-25 @ 1:07 AM
NCT ID:
NCT06381193
Brief Summary:
The goal of this clinical trial is to learn if supplementation with prebiotics and/or probiotics can lead to an improvement in symptoms of patients with functional constipation. The main objectives are:
* To evaluate the effect of the dietary supplements on the bowel frequency movements in patients with chronic functional constipation, after 8 weeks.
* To evaluate the stool consistency after 8 weeks (Bristol scale).
* To evaluate the quality of life scale score for patients with Constipation (CVE20 and GSRS scales), after 8 weeks.
Participants are randomized into the following groups:
* Group A: 20 assigned to probiotic + placebo
* Group B: 20 assigned to prebiotic + placebo
* Group C: 20 assigned to probiotic + prebiotic
* Group D: 20 assigned to the placebo + placebo
Participants took 4 units of product per day (2 of each assigned product) for 2 months.
Study:
NCT06381193
Study Brief:
Protocol Section:
NCT06381193