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NCT05614726 · ClinicalTrials.gov registry record · NA

A Probiotic Blend Reduces Gastrointestinal Symptoms and Positively Impacts Microbiota Modulation in a Randomized Study

A NA study of Constipation and Microbiota, sponsored by The Center for Applied Health Sciences.

Completed
Registry status
NA
Development phase
52
Enrollment target
1
Study location

NCT05614726 is a NA study of Constipation and Microbiota that has completed, run by The Center for Applied Health Sciences. The registered enrollment target is 52 participants, below the 204-participant average among 54 other Constipation trials with a reported enrollment target (75% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05614726, a NA study of Constipation and Microbiota, has completed, sponsored by The Center for Applied Health Sciences.

COMPLETED
Registry status
NA
Development phase
52 participants
Enrollment target
1
Study location

Study Summary

This randomized, placebo-controlled, double-blind study will determine the effect of daily supplementation with a probiotic blend in 60 apparently healthy men and women recruited at a single investigational center in Northeast Ohio (i.e., The Center for Applied Health Sciences). Subjects will attend three study visits. During Visit 1, subjects will be screened for participation \[i.e., medical history, routine blood work, background baseline diet\]. During Visits 2 and 3 subjects will complete questionnaires that assess their gastrointestinal health (e.g., abdominal discomfort/bloating, constipation, regularity, stool consistency). Visits 2 and 3 will correspond to before (week 0) and after six weeks of supplementation, respectively, with the probiotic dietary supplement or placebo.

Interventions

  • DIETARY_SUPPLEMENT 575mg [30 billion colony forming units] probiotic blend of Bifidobacterium breve, Lactobacillus acidophilus, Lacticaseibacillus rhamnosus, Saccharomyces boulardii, and alpha amylase

Study Locations (1)

Ohio

  • The Center for Applied Health Sciences - Canfield

Trial Details

FieldValue
Enrollment Target 52 participants
Start Date 2021-06-18
Est. Completion 2022-03-17
Phase NA

What the Registry Record Tells You About NCT05614726

The ClinicalTrials.gov registry entry for NCT05614726 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 52 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 204-participant average among 54 other Constipation trials with a reported enrollment target (75% lower). The listed sponsor is The Center for Applied Health Sciences, which has 12 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Constipation appearing as the primary indexed condition, and to 1 intervention - of which 575mg [30 billion colony forming units] probiotic blend of Bifidobacterium breve, Lactobacillus acidophilus, Lacticaseibacillus rhamnosus, Saccharomyces boulardii, and alpha amylase is the first listed.

NCT05614726 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT05614726 about?

NCT05614726 is a clinical study titled "A Probiotic Blend Reduces Gastrointestinal Symptoms and Positively Impacts Microbiota Modulation in a Randomized Study". This randomized, placebo-controlled, double-blind study will determine the effect of daily supplementation with a probiotic blend in 60 apparently healthy men and women recruited at a single investigational center in Northeast Ohio (i.e., The Center for Applied Health Sciences). Subjects will atten...

What is the current status of trial NCT05614726?

This trial is currently completed. It is a NA study. The enrollment target is 52 participants. The study started on 2021-06-18. Estimated completion is 2022-03-17.

What conditions does trial NCT05614726 study?

This clinical trial studies the following conditions: Constipation, Microbiota, Candida.

What interventions are being tested in trial NCT05614726?

The interventions under investigation include: 575mg [30 billion colony forming units] probiotic blend of Bifidobacterium breve, Lactobacillus acidophilus, Lacticaseibacillus rhamnosus, Saccharomyces boulardii, and alpha amylase (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT05614726?

This trial is sponsored by The Center for Applied Health Sciences, which has 12 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05614726 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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