Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07413744 · ClinicalTrials.gov registry record · Phase 2

The Gut - PRO Study

A Phase 2 study, sponsored by University of Wisconsin, Madison.

Not yet
Registry status
Phase 2
Development phase
40
Enrollment target

NCT07413744: Clinical Trial Phase 2 study, sponsored by University of Wisconsin, Madison.

NCT07413744 is a Phase 2 study that has not yet begun recruiting, run by University of Wisconsin, Madison. The registered enrollment target is 40 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07413744, a Phase 2 study, has not yet begun recruiting, sponsored by University of Wisconsin, Madison.

NOT YET RECRUITING
Registry status
Phase 2
Development phase
40 participants
Enrollment target

Study Summary

The purpose of this study is to assess the safety and feasibility of an oral probiotic supplement (PS) intervention in individuals with dementia or mild-cognitive impairment (MCI) due to Alzheimer's disease or at risk of dementia due to Alzheimer's disease (AD). 40 participants will be enrolled and can expect to be on study for up to 1 year.

Interventions

  • OTHER Placebo
  • DRUG Probiotic

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2026-08
Est. Completion 2029-03
Phase Phase 2
University of Wisconsin, Madison

1,039 total trials

What is known before NCT07413744 opens enrollment

NCT07413744 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT07413744 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07413744 about?

NCT07413744 is a clinical study titled "The Gut - PRO Study". The purpose of this study is to assess the safety and feasibility of an oral probiotic supplement (PS) intervention in individuals with dementia or mild-cognitive impairment (MCI) due to Alzheimer's disease or at risk of dementia due to Alzheimer's disease (AD). 40 participants will be enrolled and ...

What is the current status of trial NCT07413744?

This trial is currently not yet recruiting. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2026-08. Estimated completion is 2029-03.

What interventions are being tested in trial NCT07413744?

The interventions under investigation include: Placebo (OTHER), Probiotic (DRUG).

Who is sponsoring clinical trial NCT07413744?

This trial is sponsored by University of Wisconsin, Madison, which has 1,039 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07413744's enrollment target sits among peer trials

40 1362nd of 2000 higher than 542 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01306019 · 40 participants · Phase 1

    Lentiviral Gene Transfer for Treatment of Children Older Than Two Years of Age With X-Linked Severe Combined Immunodeficiency (XSCID)

  • NCT01608152 · 40 participants

    Development of a Video Game for the Improvement of Outcomes in Stem Cell Transplant Survivors

  • NCT01668082 · 40 participants · NA

    An Investigation of Brain Tumor Metabolism in Patients Undergoing Surgical Resection

  • NCT02015013 · 40 participants · Phase 2

    Hematopoietic Stem Cell Mobilization in Idiopathic CD4 Lymphocytopenia Patients and Healthy Controls for the Study of T Cell Maturation and Trafficking in Murine Models

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT07413744, the US trial registry maintained by the National Library of Medicine. NCT07413744 (small enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.