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NCT01915173 · ClinicalTrials.gov registry record · NA

Response to Supplement and Placebo in GERD

A NA study, sponsored by Beth Israel Deaconess Medical Center.

Completed
Registry status
NA
Development phase
24
Enrollment target

NCT01915173 is a NA study that has completed, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 24 participants.

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The verdict

NCT01915173, a NA study, has completed, sponsored by Beth Israel Deaconess Medical Center.

COMPLETED
Registry status
NA
Development phase
24 participants
Enrollment target

Study Summary

The purpose of this study is to investigate the effects of a widely available over the counter supplement marketed for heartburn symptoms on symptoms and health-related quality of life in patients with gastroesophageal reflux disease (GERD). This study is designed as a pilot trial to assess safety and feasibility and to provide preliminary estimates of effect sizes.

Interventions

  • DRUG Placebo
  • DRUG Supplement
  • BEHAVIORAL Expanded Interview
  • BEHAVIORAL Standard Interview

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2013-06
Est. Completion 2014-04
Phase NA

What the Registry Record Tells You About NCT01915173

The ClinicalTrials.gov registry entry for NCT01915173 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Beth Israel Deaconess Medical Center, which has 488 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.

NCT01915173 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01915173 about?

NCT01915173 is a clinical study titled "Response to Supplement and Placebo in GERD". The purpose of this study is to investigate the effects of a widely available over the counter supplement marketed for heartburn symptoms on symptoms and health-related quality of life in patients with gastroesophageal reflux disease (GERD). This study is designed as a pilot trial to assess safety a...

What is the current status of trial NCT01915173?

This trial is currently completed. It is a NA study. The enrollment target is 24 participants. The study started on 2013-06. Estimated completion is 2014-04.

What interventions are being tested in trial NCT01915173?

The interventions under investigation include: Placebo (DRUG), Supplement (DRUG), Expanded Interview (BEHAVIORAL), Standard Interview (BEHAVIORAL).

Who is sponsoring clinical trial NCT01915173?

This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.