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COMPLETED NA

Study to Evaluate a Probiotic in Healthy Subjects With a History of Abdominal Discomfort and Bloating

NCT01099696 · View on ClinicalTrials.gov ↗

Study Summary

This is a multicenter, double-blind, randomized, placebo-controlled, 6-week study of a probiotic for abdominal discomfort and bloating in healthy subjects.

Interventions

  • DIETARY_SUPPLEMENT placebo
  • DIETARY_SUPPLEMENT B. infantis 35624

Study Locations (10)

Illinois

  • Research Site — Chicago
  • Research Site — Rockford

North Carolina

  • Research Site — Chapel Hill
  • Research Site — Greensboro

Indiana

  • Research Site — Indianapolis

Maryland

  • Research Site — Chevy Chase

Ohio

  • Research Site — Cincinnati

South Carolina

  • Research Site — Greer

Tennessee

  • Research Site — Nashville

Virginia

  • Research Site — Charlottesville

Trial Details

FieldValue
Enrollment Target 302 participants
Start Date 2010-04
Est. Completion 2010-10
Phase NA

Sponsor

Procter and Gamble

25 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01099696

The ClinicalTrials.gov registry entry for NCT01099696 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 302 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Procter and Gamble, which has 25 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Bloating appearing as the primary indexed condition, and to 2 interventions — of which placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01099696 reports 10 study locations spanning 8 distinct geographic areas — top geographies include Illinois, North Carolina, Indiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01099696 about?

NCT01099696 is a clinical study titled "Study to Evaluate a Probiotic in Healthy Subjects With a History of Abdominal Discomfort and Bloating". This is a multicenter, double-blind, randomized, placebo-controlled, 6-week study of a probiotic for abdominal discomfort and bloating in healthy subjects.

What is the current status of trial NCT01099696?

This trial is currently completed. It is a NA study. The enrollment target is 302 participants. The study started on 2010-04. Estimated completion is 2010-10.

What conditions does trial NCT01099696 study?

This clinical trial studies the following conditions: Bloating, Abdominal Discomfort. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01099696?

The interventions under investigation include: placebo (DIETARY_SUPPLEMENT), B. infantis 35624 (DIETARY_SUPPLEMENT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01099696?

This trial is sponsored by Procter and Gamble, which has 25 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01099696 being conducted?

This trial has 10 study locations across Illinois, Indiana, Maryland, North Carolina, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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