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NCT00719160 · ClinicalTrials.gov registry record · Phase 4

The Effect of Protein on Calcium Absorption and Gastric Acid Production

A Phase 4 study of Osteoporosis, sponsored by Yale University.

Completed
Registry status
Phase 4
Development phase
12
Enrollment target
1
Study location

NCT00719160 is a Phase 4 study of Osteoporosis that has completed, run by Yale University. The registered enrollment target is 12 participants, below the 1,546-participant average among 84 other Osteoporosis trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00719160, a Phase 4 study of Osteoporosis, has completed, sponsored by Yale University.

COMPLETED
Registry status
Phase 4
Development phase
12 participants
Enrollment target
1
Study location

Study Summary

We have established that dietary protein is an important regulator of intestinal calcium absorption in humans. However, we do not understand the mechanism by which dietary protein is affecting calcium absorption. Therefore, the purpose of this research is to evaluate whether dietary protein-induced changes in gastric acid secretion explain the observed changes in intestinal calcium absorption.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG esomeprazole

Study Locations (1)

Connecticut

  • Yale New Haven Hospital Hospital Research Unit - New Haven

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2005-01
Est. Completion 2008-05
Phase Phase 4

Sponsor

Yale University

1,492 total trials

What the Registry Record Tells You About NCT00719160

The ClinicalTrials.gov registry entry for NCT00719160 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,546-participant average among 84 other Osteoporosis trials with a reported enrollment target (99% lower). The listed sponsor is Yale University, which has 1,492 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Osteoporosis appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT00719160 reports 1 study location spanning 1 distinct geographic area - top geographies include Connecticut.

Frequently Asked Questions

What is clinical trial NCT00719160 about?

NCT00719160 is a clinical study titled "The Effect of Protein on Calcium Absorption and Gastric Acid Production". We have established that dietary protein is an important regulator of intestinal calcium absorption in humans. However, we do not understand the mechanism by which dietary protein is affecting calcium absorption. Therefore, the purpose of this research is to evaluate whether dietary protein-induced ...

What is the current status of trial NCT00719160?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 12 participants. The study started on 2005-01. Estimated completion is 2008-05.

What conditions does trial NCT00719160 study?

This clinical trial studies the following conditions: Osteoporosis.

What interventions are being tested in trial NCT00719160?

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

Who is sponsoring clinical trial NCT00719160?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00719160 being conducted?

This trial has 1 study location across Connecticut. 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

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.