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NCT01010191 · ClinicalTrials.gov registry record · NA

Harnessing Placebo Effects: Non-Deceptive Use of Placebo in Irritable Bowel Syndrome (IBS)

A NA study of Irritable Bowel Syndrome, sponsored by Harvard University Faculty of Medicine.

Completed
Registry status
NA
Development phase
70
Enrollment target
1
Study location

NCT01010191 is a NA study of Irritable Bowel Syndrome that has completed, run by Harvard University Faculty of Medicine. The registered enrollment target is 70 participants, below the 143-participant average among 47 other Irritable Bowel Syndrome trials with a reported enrollment target (51% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01010191, a NA study of Irritable Bowel Syndrome, has completed, sponsored by Harvard University Faculty of Medicine.

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

Study Summary

Irritable bowel syndrome patients will be given either placebo pill or no treatment for a period of 3 weeks.

Conditions Studied

Interventions

  • OTHER Sugar pill

Study Locations (1)

Massachusetts

  • Beth Israel Deaconess Medical Center - Boston

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2008-07
Est. Completion 2010-04
Phase NA

What the Registry Record Tells You About NCT01010191

The ClinicalTrials.gov registry entry for NCT01010191 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 143-participant average among 47 other Irritable Bowel Syndrome trials with a reported enrollment target (51% lower). The listed sponsor is Harvard University Faculty of Medicine, which has 9 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Irritable Bowel Syndrome appearing as the primary indexed condition, and to 1 intervention - of which Sugar pill is the first listed.

NCT01010191 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT01010191 about?

NCT01010191 is a clinical study titled "Harnessing Placebo Effects: Non-Deceptive Use of Placebo in Irritable Bowel Syndrome (IBS)". Irritable bowel syndrome patients will be given either placebo pill or no treatment for a period of 3 weeks.

What is the current status of trial NCT01010191?

This trial is currently completed. It is a NA study. The enrollment target is 70 participants. The study started on 2008-07. Estimated completion is 2010-04.

What conditions does trial NCT01010191 study?

This clinical trial studies the following conditions: Irritable Bowel Syndrome.

What interventions are being tested in trial NCT01010191?

The interventions under investigation include: Sugar pill (OTHER).

Who is sponsoring clinical trial NCT01010191?

This trial is sponsored by Harvard University Faculty of Medicine, which has 9 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01010191 being conducted?

This trial has 1 study location across Massachusetts. 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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