Pure Global

Effect of L. Paracasei Strain Shirota on Constipation in Healthy US Adults - Trial NCT06014008

Access comprehensive clinical trial information for NCT06014008 through Pure Global AI's free database. This phase not specified trial is sponsored by Yakult U.S.A. Inc. and is currently Not yet recruiting. The study focuses on Constipation. Target enrollment is 50 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

Free Database
Powered by Pure Global AI
840K+ Trials
NCT06014008
Not yet recruiting
other
Trial Details
ClinicalTrials.gov โ€ข NCT06014008
View on ClinicalTrials.gov
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Effect of L. Paracasei Strain Shirota on Constipation in Healthy US Adults
The Effect of Lacticaseibacillus Paracasei Strain Shirota (LcS) in Healthy US Individuals Suffering From Hard or Lumpy Stools: A Randomized Controlled Open Trial.

Study Focus

Constipation

Test product consumption group

Interventional

other

Sponsor & Location

Yakult U.S.A. Inc.

Timeline & Enrollment

N/A

Aug 01, 2023

Aug 01, 2024

50 participants

Primary Outcome

Proportion of subjects that produce hard or lumpy stools (Subjectively evaluated Bristol stool form scale (BSFS) score of 1 or 2, ) โ‰ฅ 25% of bowel movements.

Summary

The objective of this study is to investigate the efficacy of daily consumption of a
 fermented milk containing LcS in reducing the frequency of bowel movement with hard or lumpy
 stools in generally healthy U.S. adult population with intermittent bowel movements producing
 hard or lumpy stools.

ICD-10 Classifications

Constipation
Irritable bowel syndrome with predominant constipation [IBS-C]
Other laxatives
Poisoning: Other laxatives
Other functional intestinal disorders

Data Source

ClinicalTrials.gov

NCT06014008

Non-Device Trial